The scope of this page is pediatric traumatic brain injury (ages birth through 21 years). ASHA has a separate Practice Portal page on Traumatic Brain Injury in Adults.
See ASHA’s Pediatric Brain Injury Evidence Map for summaries of the available research on this topic.
Traumatic brain injury (TBI) is an acquired brain injury that results from a bump, blow, or jolt to the head (or body) or a penetrating head injury that disrupts normal brain function (Centers for Disease Control and Prevention [CDC], 2015).
TBI can cause focal brain damage (e.g., gunshot wound), diffuse (e.g., abusive head trauma), or both.
Diffuse axonal injury (DAI) is a type of TBI that is caused by a blunt injury to the brain that stretches and disconnects white-matter tracts. DAI is often invisible on an initial computed tomography (CT) scan but can be associated with prolonged coma and long-term disability. DAI is often classified as severe TBI (Mesfin et al., 2025).
TBI can slow, interrupt, alter, or halt brain development, which can delay the visibility of deficits until expected skills fail to emerge. TBI in children is a chronic disease process rather than a one-time event, because symptoms may change and unfold over time (Masel & DeWitt, 2010). Pediatric TBI can be a lifelong condition and may require ongoing, developmentally appropriate strategies that support their growth, independence, and participation across the lifespan. According to the CDC, 70%–80% of children with mild TBI (mTBI) will demonstrate functional recovery by 1–3 months (CDC, 2018).
TBI can result from a primary injury or a secondary injury (see common classifications of TBI for more details). TBI is typically classified as mild, moderate, or severe based on (a) the extent and nature of the injury; (b) the duration of loss of consciousness; (c) posttraumatic amnesia (PTA; i.e., loss of memory for events immediately following injury); and (d) the severity of confusion at initial assessment during the acute phase of injury (Diagnostic and Statistical Manual of Mental Disorders [5th ed.; American Psychiatric Association, 2022]; CDC, 2015).
The National Institutes of Health National Institute of Neurological Disorders and Stroke (NINDS) has launched an international initiative to develop a new model to classify the acute phase of TBI more accurately. This approach includes clinical, biomarker, imaging, and modifier pillars (CBI-M). These modifiers are important to consider in pediatric TBI because they may impact recovery and characterize severity. Modifiers may include
For further information, see Manley et al. (2025).
This new model does not offer specific recommendations to classify pediatric TBI severity. TBI is often diagnosed based on findings from imaging (i.e., CT, magnetic resonance imaging, or positron emission tomography scans) and ratings on the Glasgow Coma Scale (GCS; Teasdale et al., 2014) a numerical tool used to assess TBI severity.
The pediatric GCS has been modified since its initial inception, and no single modification is universally accepted. Per modifications made by James (1986) and the Pediatric Emergency Care Applied Research Network, it can be used in preverbal children who are younger than 2 years and verbal children who are older than 2 years. The GCS can be used in children 5 years and older without modification (Munakomi et al., 2026).
mTBI can present with no overt neuroimaging findings or may be visible on high resolution computed tomography (HCT), computed tomography (CT), or magnetic resonance imaging (MRI).
Concussion, a form of mTBI, is an injury to the brain that may or may not involve a brief loss of consciousness. It is otherwise characterized by the same physical and cognitive sequelae as TBI. Concussion typically occurs due to a blow, bump, or jolt to the head, face, neck, or body (McCrory et al., 2013).
The term “concussion” is often used interchangeably with the term “mTBI” (Silverberg et al., 2021). Consistent use of “mTBI” may be more appropriate than “concussion” for documentation and patient education because it helps prevent misinterpretation of the different terms (Centers for Disease Control and Prevention Guideline on the Diagnosis and Management of Mild Traumatic Brain Injury Among Children, 2020).
Incidence of pediatric TBI refers to the number of new cases identified in a specified time period. Prevalence of TBI refers to the number of children who are living with the condition in a given time period.
Incidence and prevalence rates of pediatric TBI vary across clinical and epidemiological studies. These variations are often due to differences in participant characteristics (e.g., ages included), diagnostic classification criteria within and across subtypes (e.g., mTBI vs. severe TBI), and sources of data (e.g., hospital admissions, emergency room visits, general practitioner visits). Moreover, current statistics do not take into account children and adolescents who do not seek medical care. Therefore, these estimates may significantly underestimate the incidence and prevalence of pediatric TBI.
Regardless of variations, TBI is the leading cause of disability and death in children ages 0–4 years and adolescents ages 15–19 years (CDC, 2015). Also, it is estimated that 145,000 children and adolescents (ages 0–19 years) are living with lasting cognitive, physical, or behavioral effects of TBI (Zaloshnja, Miller, Langlois, & Selassie, 2008).
Signs and symptoms vary depending on the severity of the TBI; Diagnostic and Statistical Manual of Mental Disorders [5th ed.; American Psychiatric Association, 2022]; CDC, 2015; Haarbauer-Krupa & Brink, 2020).
Although some children with TBI maintain typical developmental progression, others may have long-term cognitive difficulty.
Long-term effects happen because the pediatric brain is still developing (Agrawal et al., 2026). For example, sensory systems and the frontal lobes of the brain develop in childhood and continue to develop through late adolescence and into the second decade of life (S. J. Taylor et al., 2013).
Pediatric TBI often affects academic performance (Kingery et al., 2017). Monitoring children with TBI as academic demands increase is important (e.g., moving from elementary to middle school). As demands increase, deficits may become more apparent when they impact a child’s ability to achieve.
Functional difficulties include learning new information and negotiating complex social interactions (Anderson et al., 2012; Turkstra et al., 2015). These difficulties can affect multiple factors (Allonsius et al., 2024; Lundine et al., 2026; Shankar et al., 2018; Wehman et al., 2014). Such factors may include
The full sequelae of pediatric TBI can emerge and/or persist well into adulthood, which is why pediatric TBI should be considered a chronic disease process rather than a one-time event (DePompei, 2010; Masel & DeWitt, 2010).
Infants and toddlers may lack the communication or developmental skills to report signs and symptoms of TBI. Sometimes, there are no apparent external physical signs to indicate a TBI, and attention to behavioral symptoms is critical (Cox, 2016). Clinicians and caregivers need to be aware of the following signs that may be initially observed after TBI for this age group:
Per Dupont et al. (2024), postconcussive symptoms may include
For more information regarding the signs and symptoms of concussion in this population, please see Dupont et al. (2021) and Beauchamp et al. (2024).
Many cognitive skills are undeveloped in infants and toddlers, and TBI can affect the development of these skills. This population must be carefully monitored, as signs and symptoms may become apparent later in life as expected skills fail to develop or emerge more slowly (e.g., when a child is challenged academically; Anderson et al., 2005; McKinlay & Anderson, 2013).
The neurodevelopmental and physical characteristics of infants and toddlers can increase the risk of TBI as compared to adults (e.g., larger head-to-body ratio than adults or older children).
See the Assessment and Treatment sections for more information about young children with TBI.
The causes of pediatric TBI are varied and appear to differ by age. The Centers for Disease Control and Prevention (CDC) identified the following leading causes of TBI in children and adolescents aged 0–14 years:
Falls and assault (e.g., abusive head trauma or other physical abuse) are the most common mechanisms of TBI in infants, toddlers, and preschoolers. TBI secondary to velocity injury (e.g., motor vehicle or bicycle accidents, sports injuries) occurs more often in elementary school children and adolescents (Faul et al., 2010).
SLPs do not diagnose TBI; however, they play a key role in the screening, assessment, and treatment of children and adolescents with TBI. The professional roles and activities in speech-language pathology include clinical services (assessment, planning, and treatment), prevention, and advocacy, as well as education, administration, and research. See ASHA’s Scope of Practice in Speech-Language Pathology (ASHA, 2016).
Appropriate roles for SLPs include the following:
As indicated in the ASHA Code of Ethics (ASHA, 2023), SLPs who serve this population should be specifically educated and appropriately trained to do so.
Audiologists play a central role in the assessment, diagnosis, and rehabilitation of hearing and vestibular deficits in children and adolescents with TBI. See ASHA’s Scope of Practice in Audiology (ASHA, 2018).
Appropriate roles for audiologists include the following:
Collaboration and teaming are integral to speech-language pathology and audiology service delivery for children with TBI. Integration of knowledge and skills from a variety of disciplines is essential for identifying functional abilities; determining the levels of support needed across clinical domains and service delivery settings; maximizing outcomes; and facilitating transition back to home, school, and community. Team members may include physicians, physical and occupational therapists, teachers, neuropsychologists, and school psychologists.
Team models vary (see ASHA’s resource on collaboration and teaming). The model selected will depend on the needs of the child and their family. The role that each team member plays will evolve as the child or adolescent develops and as their needs change.
The roles of the SLP and the audiologist will be guided by each profession’s scope of practice, discipline-specific training, ethical considerations, and state licensure regulations. See ASHA's State-by-State for more information.
For further reading, please see Haarbauer-Krupa et al. (2017) and Alessi et al. (2026).
See the Traumatic Brain Injury section of the Pediatric Brain Injury Evidence Map for pertinent scientific evidence, expert opinion, and client/caregiver perspective.
Children and adolescents with TBI have varied and complex sequelae that can change over time. Assessment considers the child’s behaviors, strengths, and needs over the course of development and rehabilitation, including school and community reentry. It is helpful to focus childhood assessment on areas that are critical to learning and school success.
Assessment requires ongoing collaboration with the family and medical, surgical, rehabilitation, and educational professionals. Findings from the speech-language and audiologic assessments are analyzed in the context of findings from other professionals on the team. See ASHA’s webpage on Interprofessional Education/Interprofessional Practice (IPE/IPP).
Note that mental health concerns are common after pediatric TBI (Max et al., 2022), and clinicians should look for potential indicators (e.g., premorbid history of psychiatric disorder) and refer to appropriate health care providers (e.g., psychiatrists and psychologists) as necessary.
Screening is conducted by audiologists and SLPs to identify possible deficit areas following a TBI. Screening is typically completed prior to conducting more comprehensive evaluations.
Screening identifies the need for further assessment but does not provide a detailed description of severity or symptoms. Screening may result in recommendations for rescreening, comprehensive assessments, or referral for other examinations or services.
Hearing screening and otoscopic inspection ideally occur prior to screening for other deficits. If the child has a history of hearing loss, they would not be appropriate for hearing screening. In this case, follow-up audiologic assessment would be appropriate to determine if the TBI added to the existing hearing loss.
Hearing screening is within the SLP scope of practice. See ASHA’s Practice Portal page on Childhood Hearing Screening.
A referral for a full audiologic evaluation is necessary if the child fails the hearing screening or if hearing loss is suspected. Audiologists may also assess auditory processing, tinnitus, and vestibular function as indicated. See ASHA’s Practice Portal pages on Hearing Loss in Children, Hearing Loss in Adults, Tinnitus and Hyperacusis, and Balance System Disorders.
SLPs screen for speech, language, cognitive-communication, and swallowing deficits. Due to a lack of validated screening tools for this population, recommendations and referrals are often based on developmental expectations (Turkstra et al., 2015). Screening typically includes interviews with family members and/or teachers regarding concerns about the child’s skills. Screening that involves such interviews can also occur in the school setting prior to SLP involvement. In this case, screening may identify previously unrecognized TBIs and/or indicate SLP involvement in assessment and treatment (Perrier et al., 2026). Screening is conducted in the language(s) used by the child and family, with consideration of cultural and linguistic variables.
The purpose of a comprehensive assessment for children with TBI is to determine speech, language, cognitive-communication, and swallowing abilities; identify strengths and deficits; and determine appropriate interventions. The specific focus of a comprehensive assessment can vary depending on the child’s current age and the child’s age at the time of injury, the injury’s severity, the stage of recovery, and prior educational status. Ongoing assessment is necessary to evaluate performance and to track changes in functioning as the child recovers from TBI.
Factors that may influence assessment include the following:
If a child wears prescription eyeglasses or hearing aids and prescriptions are still appropriate post-injury, the glasses or aids should be worn during assessment.
If the TBI resulted in additional hearing or visual deficits, sensory aids and/or accommodations that were used premorbidly may no longer be sufficient for the child, and physical or environmental modifications may be needed (e.g., large-print material, modified lighting, amplification devices).
If changes to premorbid hearing and/or vision are suspected, refer the individual for complete audiologic and/or vision assessments prior to any additional testing. (See ASHA’s Practice Portal pages on Hearing Loss in Children and Hearing Loss in Adults.)
Comprehensive assessment uses both standardized and nonstandardized procedures to help identify areas of weakness, areas of strength, and/or effective educational supports. See ASHA’s resources on assessment tools, techniques, and data sources and dynamic assessment. Functional assessment that includes information from multiple sources (e.g., caregivers, teachers) should be considered to give a better idea of the child’s specific areas of need and how they function in situations that are relevant to their lives (Riccardi et al., 2022).
Ongoing monitoring of cognitive function is necessary due to potential developmental impacts, latent presentation of deficits, and changing environmental expectations (Haarbauer-Krupa et al., 2017).
When selecting standardized assessments, consider the following:
Functional or situational assessments (e.g., language sampling, analog tasks, and naturalistic observation) and anecdotal reports can supplement data from standardized tests. Due to the limitations in standardized assessments, nonstandardized assessment is a critical component of any comprehensive evaluation for youth with TBI.
Nonstandardized measures that focus on process rather than content knowledge may provide valuable information for targeting interventions and identifying effective treatment strategies (Turkstra et al., 2015). These procedures may provide information about the ability of children with TBI to function in real-world contexts (Hall et al., 2021).
Nonstandardized assessments can add insight into a school-age child’s functioning in natural environments (Lundine & Hall, 2020) and may answer questions such as the following:
See ASHA’s Practice Portal page on Childhood Hearing Screening.
See the Assessment section of ASHA’s Practice Portal page on Speech Sound Disorders: Articulation and Phonology.
See the Assessment sections of ASHA’s Practice Portal pages on Childhood Apraxia of Speech and Acquired Apraxia of Speech.
See the Assessment section of ASHA’s Practice Portal page on Voice Disorders.
See the Assessment sections of ASHA’s Practice Portal pages on Spoken Language Disorders and Late Language Emergence.
See the Assessment section of ASHA’s Practice Portal page on Written Language Disorders.
See the Assessment section of ASHA’s Practice Portal page on Social Communication Disorder.
See ASHA’s Practice Portal page on Augmentative and Alternative Communication (AAC).
See the Assessment section of ASHA’s Practice Portal page on Pediatric Feeding and Swallowing.
See the Assessment sections of ASHA’s Practice Portal pages on Hearing Loss in Children and Hearing Loss in Adults.
See the Assessment sections of ASHA’s Practice Portal pages on Balance System Disorders and Tinnitus and Hyperacusis.
Comprehensive assessment typically results in one or more of the following:
Assessments are informed by a person’s cultural and linguistic background and are completed in the language(s) used by the individual with TBI (see ASHA’s Practice Portal pages on Multilingual Service Delivery in Audiology and Speech-Language Pathology; Cultural Responsiveness; and Collaborating With Interpreters, Transliterators, and Translators). TBI may affect each language used by the child in different ways. Therefore, information about all languages should be collected. Any accommodations and modifications related to native language or culture must be documented. Standard scores should not be reported if a standardized test is modified or translated, as norms will not apply.
Conversational and nonverbal norms vary widely across cultures. Clinical judgment should not be based solely on the clinician’s experience of what is appropriate or should be expected. Instead, clinicians consider each child’s cultural and linguistic norms when assessing factors that require subjective judgments (e.g., initiation and response time, turn-taking in conversations, topic maintenance).
TBI often causes deficits in cognition and language. It is important to recognize the overlap and distinctions between these two domains. Language impairment can disrupt cognitive processes (e.g., attention, memory, and executive functions). An impairment of cognitive processes can also disrupt aspects of language (e.g., syntax, semantics, and pragmatics). Assessment identifies strengths and deficits in these related domains. Difficulty with any aspect of communication that is affected by disruption of cognition is diagnosed as a cognitive-communication disorder.
The following may have an impact on the assessment of feeding and swallowing:
See also the Assessment section of ASHA’s Practice Portal page on Pediatric Feeding and Swallowing.
Children with superior canal dehiscence or enlarged vestibular aqueduct are more susceptible to hearing and balance problems after TBI. Audiologists need to be aware of the potential impact of these conditions during assessment. Promoting hearing wellness and monitoring the acoustic environment are also key roles for the audiologist in assessment. See ASHA’s Practice Portal page on Balance System Disorders.
One of the main challenges in assessing infants, toddlers, and preschoolers is a lack of objective information regarding pre-injury function on which to base an evaluation of deficits (Haarbauer-Krupa & Brink, 2020). Cognitive-communication skills are still developing during this period, making symptoms difficult to evaluate, particularly in preverbal children. Ongoing assessment at various points post-injury is critical to monitor for emerging deficits, particularly as cognitive-communication demands increase. It is also essential that caregivers understand the necessity of informing schools about the child’s TBI as they transition to formal schooling (i.e., kindergarten). Structured interviews with parents or caregivers of preschool-age children may help provide information about symptoms (Lundine, Ciccia, & Brown, 2019).
There are few standardized tests for young children with TBI (Haarbauer-Krupa & Brink, 2020); therefore, observation and parent report are key components in determining changes in baseline function or differences from developmental norms. When interpreting assessment results for children ages 0–5 years, it is important to consider
Social skills and academic performance are considered during assessment (Riccardi et al., 2025). Academic success is connected to each child’s social, behavior regulation, and cognitive abilities. Demands on cognitive and social skills increase as children graduate from each grade level. For this reason, deficits that went unnoticed at an early age might become apparent as the child gets older (Crook et al., 2023).
Ideally, cognitive-communicative development is monitored through high school and during the transition to postsecondary educational or vocational settings to help identify any previously missed deficits. Strategies to maximize functional outcomes and life participation can be implemented as deficits are discovered.
See the Traumatic Brain Injury section of the Pediatric Brain Injury Evidence Map for pertinent scientific evidence, expert opinion, and client/caregiver perspective.
Each child with TBI has a unique profile of strengths and needs. In developing a treatment plan, clinicians consider age, previous levels of function, and developmental status as well as functioning in related areas, such as sensory and motor skills.
Preexisting cognitive-communication deficits, including, but not limited to, attention-deficit/hyperactivity disorder and autism spectrum disorder, should also be considered.
Treatment is ideally functional and individualized. It addresses the ability to effectively function in everyday environments (e.g., home, school, work, and community). Treatment can focus on developing and generalizing new skills, remediating lost functions, and/or addressing unwanted behaviors (Crook et al., 2023).
Every child and family has a unique set of circumstances (e.g., cultural background, medical and developmental history, learning styles, social determinants of health) that can affect treatment. Treatment is individualized; provided in the language(s) used by the individual; and done with consideration of their values, needs, and preferences. See ASHA’s Practice Portal pages on Multilingual Service Delivery in Audiology and Speech-Language Pathology; Collaborating With Interpreters, Transliterators, and Translators; and Cultural Responsiveness.
Family-centered practice is the foundation of intervention for pediatric TBI. Treatment outcomes and reintegration into home, school, work, and community environments for children with TBI are best achieved when family members and caregivers play a central role (Lundine, Utz, et al., 2019). These individuals are responsible for making decisions that affect the child’s life and education and provide long-term supports (Roscigno & Swanson, 2011).
Family members and caregivers can be frightened, stressed, and overwhelmed by the magnitude of the medical situation, changes in their child, and the process of learning to care for a child with TBI (Wade et al., 2006). Effective education, training, and counseling require sensitivity to these emotions.
Per Lundine et al. (2026), caregivers may have the following concerns:
Family-centered practice targets the family’s ability to adapt to changes brought about by TBI. Clinicians can assist by helping family members communicate openly, identify priorities, and learn how to solve problems together.
Proper education and emotional support can help bolster families’ innate ability to work with and assist their children. This assistance can help them manage the cognitive, behavioral, communication, and other life changes associated with TBI (Gan et al., 2013).
Family-centered practice provides opportunities for family members and caregivers to
The roles of family members and caregivers vary based on individual needs; the severity of injury; family circumstances; cultural dimensions; and attitudes, beliefs, and expectations (Roscigno & Swanson, 2011). See also ASHA’s resource on focusing care on individuals and their care partners.
For further information, please see Jenkin et al. (2022, 2025) and Laatsch et al. (2020).
A variety of treatment approaches can be used in intervention for children with TBI. These approaches are listed separately below but are not mutually exclusive. Often, aspects of more than one approach are integrated in the delivery of speech and language services.
For further information related to treatment for pediatric TBI, see Laatsch et al. (2020) and Crook et al. (2023).
Restorative approaches involve direct therapy aimed at improving or restoring impaired function(s) through retraining. Treatment is often hierarchical, exercising target-specific processes in the impaired domain before introducing more demanding higher level tasks in that domain and eventually generalizing skills to more functional activities and tasks (ASHA, 2003; Sohlberg & Mateer, 2001).
Habilitative approaches target skills that have not yet developed. Habilitative interventions help children learn, keep, or improve skills and functional abilities following their injury rather than restore skills that they had mastered prior to injury. These approaches often are used in treatment when the injury occurs before some developmental milestones have been met (e.g., cognitive, speech and language, or swallowing). Skills that are not yet fully developed at the time of TBI may be particularly vulnerable post-injury.
As cognitive, behavioral, academic, and social demands increase over time, children with TBI may demonstrate additional deficits not seen immediately following injury (Anderson et al., 2005; Gamino et al., 2009). Habilitative approaches may also be needed at this point to facilitate learning.
Compensatory approaches focus on adapting to deficits by learning new or different ways of doing things to minimize difficulties (National Institutes of Health, 1998). Compensatory approaches use a child’s strengths to maximize their abilities, often through the use of external or internal aids (Blosser & DePompei, 2003; Shum et al., 2011).
A compensatory approach to treatment may also include accommodations and/or modifications.
For further information, please see Ylvisaker and Feeney (1998).
Accommodations are changes to the environment, task, or mode of response that allow an individual to access and participate in an activity without changing the activity itself. Academic accommodations can help students with TBI demonstrate their knowledge and skills by reducing the impact of injury-related challenges, allowing them to engage with learning in ways that reflect their true capabilities (Childers & Hux, 2013).
Academic accommodations for students with TBI may include
An accommodation may be required as part of a Section 504 plan or as part of an individualized family service plan (IFSP) or individualized education program (IEP).
Modifications are changes to the nature of an activity to facilitate participation and promote success in home, community, school, and work settings. Academic modifications can include changes in materials, curriculum content, or acceptable responses (New York State Education Department, 2002).
Modifications for students with TBI may include shortened class schedule or day, reduced number or type of assignment, or modified response type (e.g., multiple-choice questions instead of recall questions or short-answer questions).
External aids are used to facilitate improved attention, time management, organization, and recall of events and information (Burns, 2004; Teasell et al., 2013). Headphones, computers, and handheld devices, including smartphones and voice recorders, may serve as functional external aids for children; low-tech options include calendars, timers, checklists, maps, color-coded binders, and small notebooks (Burns, 2004; DePompei et al., 2008). Training children with TBI to use these strategies independently requires structured, sequenced, and repetitive practice and needs to take into consideration the child’s level of deficit awareness (Sohlberg et al., 2007; Ylvisaker, 1998). Clinicians consider the most appropriate option for each individual when selecting and training the use of external aids to facilitate cognitive-communication function in everyday activities (Wild, 2013, 2014).
Internal aids are mental strategies used to enhance memory and executive function. Examples include mnemonics, visual imagery, association, elaborative encoding, and chunking. For example, mnemonics and visual images can help improve recall for names (Kaschel et al., 2002; OʼNeil-Pirozzi et al., 2015). With elaborative encoding, individuals learn to associate new information with related features or information already in memory (Oberg & Turkstra, 1998). Grouping or chunking information into logical categories can be used when large amounts of information need to be remembered (Kennedy, 2006).
Functional/contextualized approaches focus on personally meaningful goals, routines, and activities with generalization of skills to relevant social, vocational, and educational activities. Contextualized interventions for children and adolescents with TBI are functional, personally relevant, nonhierarchical, and collaborative (Koole et al., 2015). They involve teaming with educators, caregivers, and peers to facilitate carryover of skills to situations and activities of interest and importance to the child and family.
Functional goals consider the child’s and caregivers’ priorities and promote independence, generalization, and community competence across settings (Feeney & Ylvisaker, 2008; Sohlberg & Turkstra, 2011; Ylvisaker, Adelson, et al., 2005).
Goal attainment scaling (GAS) is one collaborative approach for identifying and quantifying individualized, meaningful treatment outcomes by using a point scale to objectively measure goal achievement (Kiresuk et al., 2014). GAS targets executive functions by helping children identify their own goals and plan and manage their related behaviors while engaging in everyday life activities (Grant & Ponsford, 2014).
The following are brief descriptions of both general and specific treatments for individuals with deficits and disorders associated with TBI. This alphabetized list is not exhaustive, and the inclusion of any specific treatment does not imply endorsement by ASHA.
AAC involves supplementing or replacing oral speech and/or writing with aided symbols (e.g., Picture Exchange Communication System [PECS], line drawings, Blissymbols, speech-generating devices, and tangible objects) and/or unaided symbols (e.g., manual signs, gestures, and finger spelling).
Factors that influence the selection and use of AAC systems following TBI include the child’s communication abilities and needs as well as their cognitive, neurobehavioral, motor, sensory, and perceptual impairments (Fager & Spellman, 2010).
AAC intervention is an ongoing and dynamic process because the needs can vary over time, depending on the stage of recovery, the presence of cognitive–behavioral changes, and communication needs in particular settings. The training of teachers, staff, and family members for the purpose of optimizing functional communication is also an essential part of AAC intervention (Fager & Spellman, 2010). See ASHA’s Practice Portal page on Augmentative and Alternative Communication (AAC).
Behavioral intervention is used to teach desired behaviors and is based on behavioral/operant principles of learning (i.e., differential reinforcement, modeling, prompting, and fading). Injuries to the frontal lobe can result in behaviors—such as agitation, aggression, impulsivity, and self-injury—that interfere with a child’s functioning in home, community, and school environments and with their ability to communicate effectively. Behavioral interventions are often used to decrease unwanted behaviors and teach functional alternative behaviors.
Post-TBI behavioral interventions include the following:
Cognitive-communication intervention can address discrete components of the child’s cognitive-communication domains (e.g., memory, attention) or focus more globally on functional communication. Clinicians select interventions and use tools that are appropriate for the child’s current age and current level of development.
Cognitive-communication treatment methods can include direct remediation (e.g., breaking the target into discrete steps and sequentially completing a task) or strategy-based training and accommodations (e.g., training the individual to develop internal strategies to perform complex tasks, making changes in the classroom). Treatment approaches may overlap. Clinicians use the approach or approaches that best meet the child’s needs (Turkstra et al., 2015; Ylvisaker, Adelson, et al., 2005).
Cognitive deficits can impact a child’s ability to participate in therapy. For example, poor insight into deficits may affect treatment buy-in, strategy use, or adherence to recommendations.
Computer-assisted treatment refers to the use of specially designed software programs to improve cognitive-communication functions through repeated, structured practice of tasks related to cognitive domains (e.g., attention, memory), language, and speech. These programs are available for use on computers, smartphones, and tablets. Computer-assisted treatment can be used and monitored by a clinician in person or remotely, providing consistent feedback to the individual (e.g., Politis & Norman, 2016; Teasell et al., 2013).
This type of intervention does not refer to the use of computers or electronic devices (e.g., electronic memory aids or web-based organizational assistants) as external aids.
See considerations for selecting technology or related treatment products.
Direct attention training (DAT) provides structured opportunities for repeated practice to improve various aspects of attention, including sustained attention over time (vigilance), selective attention, divided attention, and the ability to shift attention (Sohlberg, 2002; Sohlberg et al., 2003). Repetitive drills provide opportunities for practice on tasks that impose increasingly more complex attentional demands (Sohlberg et al., 2003; Sohlberg & Mateer, 2001).
Metacognitive skills training is an integral part of DAT when used to treat cognitive-communication deficits in children with TBI (e.g., Lee et al., 2012; Sohlberg et al., 2014).
Drill and practice is the repetition of a specific therapy activity or target. Repetitive-drills Using a repetitive drill-and-practice technique assumes that neural networks underlying performance are strengthened by repeated activation (Sohlberg et al., 2014).
Spaced, or distributed, practice is a drill-and-practice technique in which practice is broken up into several short sessions over a longer period of time. Recall and carryover of information is better when practice trials are spaced or distributed rather than massed (Sohlberg et al., 2005; Sohlberg & Turkstra, 2011).
Drill and practice can be part of the learning process of a new skill. However, clinicians work to transfer these developing skills as soon as possible from drill into an ecologically valid environment (i.e., the classroom) to assist with generalization and learning.
Dual-task training focuses on improving task complexity by targeting the ability to carry out two competing tasks simultaneously. Dual-task training aims to restore executive functions that are often affected by TBI; it is sometimes used to train tasks across both physical and cognitive-communication domains (Valovich, McLeod, & Guskiewicz, 2012).
Errorless learning is a treatment method in which the clinician tries to minimize errors as the individual learns a targeted skill by
Errorless learning is most beneficial for individuals with relatively unimpaired procedural memory and severely impaired declarative memory (Sohlberg et al., 2005). Spaced retrieval (Sohlberg et al., 2005; Sohlberg & Turkstra, 2011) and the method of vanishing cues (Sohlberg et al., 2005) are based on principles of errorless learning.
Metacognitive skills training—also called “metacognitive strategy instruction”—focuses on improving awareness, self-monitoring, self-regulation, and use of goal-setting strategies to facilitate learning and behavioral success. Strategies such as mental imagery, self-talk, self-reflection, and keeping an agenda are used to work through problem situations, provide feedback, and track progress toward goals. Metacognitive skills training can be integrated with DAT (Sohlberg et al., 2005, 2014; Sohlberg & Turkstra, 2011).
Clinicians use project-based intervention to help improve cognitive-communication function and social engagement. Intervention facilitates participation in meaningful activities by involving individuals in a long-term, collaborative project that results in a tangible product. Projects often target competence in planning, organizing, social interaction, and self-regulation (Ylvisaker, Feeney, & Capo, 2007).
Treatment for disorders of consciousness—previously referred to as “coma stimulation”—is the systematic exposure of an individual with severe TBI to a variety of visual, auditory, tactile, olfactory, and kinesthetic stimuli to improve arousal and level of consciousness and to prevent sensory deprivation. Intensity and frequency of stimulation can be tailored to a child’s threshold to elicit a meaningful behavioral response and to monitor changes in responsiveness during recovery (Hotz et al., 2006).
For further information, please see Slomine and Suskauer (2024) and Giacino et al. (2018).
Strategic learning intervention targets the ability to synthesize disparate information (e.g., from text, lectures) into core concepts. This ability typically develops in early adolescence; it is often deficient in youth with TBI and may result in academic challenges.
Training is hierarchical and strategy based rather than content based, often incorporating text-based materials from the child’s schoolwork. The Strategic Memory and Reasoning Training (SMART) program is one example of a strategic learning intervention that teaches the student how to eliminate unimportant information, summarize information in one’s own words, and consider multiple interpretations (Cook et al., 2011).
For further information about collaborative intervention related to goals that are relevant to the child and their caregivers, please see Ylvisaker and Feeney (1998).
In task analysis, a target skill is analyzed or broken down into a sequence of smaller steps that can be taught one step at a time and then chained together. In this way, tasks that seem complex and difficult to learn become more manageable as smaller units (Sohlberg et al., 2005). This process can be applied to skills in any of the cognitive-communication domains.
Language deficits can exist in isolation or in conjunction with cognitive-communication deficits. For example, deficits in working memory may impact a child’s ability to fluently engage in conversation (Ewing-Cobbs & Barnes, 2002).
Language intervention varies depending on the child’s developmental level at the time of injury and their specific deficits.
For younger children, language intervention tends to emphasize
For older children and adolescents, the emphasis of language intervention is often on
Regardless of age at injury, treatment goals for children with TBI might also address the appropriate use of social language in different contexts and under varying demands (Blosser & DePompei, 2003; Ewing-Cobbs & Barnes, 2002; Turkstra et al., 2015).
For further information, see ASHA’s Practice Portal pages on Late Language Emergence, Spoken Language Disorders, Written Language Disorders, and Aphasia.
Social communication intervention for children and adolescents with TBI frequently focuses on training the child’s communication partners (Togher, 2014; Togher et al., 2010, 2013; Ylvisaker & Feeney, 2007; Ylvisaker, Turkstra, & Coelho, 2005). It also focuses on helping school personnel provide the necessary supports, structure, and instruction to help students learn (or relearn) appropriate behaviors and social skills in real-world communications (MacDonald & Wiseman-Hakes, 2010; New York State Education Department, 2002; New Zealand Guidelines Group, 2006).
Social communication intervention helps children develop conversation skills, learn pragmatic language norms (e.g., taking turns, remaining on topic, inhibiting confabulations), and practice impulse control necessary for improved social interactions (Burns, 2004; McDonald et al., 2014).
Intervention in the context of natural environments may incorporate supports such as structured feedback, use of videotaped interactions, modeling and role play, rehearsal and coaching, and training in self-regulation and self-monitoring strategies (MacDonald & Wiseman-Hakes, 2010; Sohlberg & Turkstra, 2011; Ylvisaker, Turkstra, & Coelho, 2005).
See ASHA’s Practice Portal page on Social Communication Disorder for additional information.
Speech intervention addresses problems that result from TBI, such as dysarthria, apraxia, phonation, resonance, respiration, articulation, and/or fluency disorders. Traditional approaches to remediation of these clinical disorders can be used in children with TBI. See ASHA’s Practice Portal pages on Childhood Apraxia of Speech; Acquired Apraxia of Speech; Speech Sound Disorders-Articulation and Phonology; Cleft Lip and Palate; Voice Disorders; and Stuttering, Cluttering, and Fluency.
Intervention for speech problems may focus on the individual speech subsystems of respiration, phonation, articulation, and velopharyngeal function or, more globally, on overall speech intelligibility using behavioral and instrumental treatments, prosthetics, compensatory strategies, AAC, and/or environmental modifications (McDonald et al., 2014; Morgan et al., 2010; Morgan & Vogel, 2008).
Children who are unable to effectively communicate with speech or sign (e.g., due to severe dysarthria, a voice disorder, or motor issues) may need AAC (Doyle & Fager, 2011).
Some children with TBI may initially be unable to speak because they have had a tracheotomy. In these cases, a speaking valve may be used to facilitate voicing.
Underlying speech subsystems may still be developing at the time of injury in pediatric populations, or the child may have preexisting speech deficits. Therefore, clinicians need to consider previous levels of function and developmental status when planning treatment. Cognitive status post-injury is also considered, because a child may appear to have apraxia when the impairment is really one of higher level executive functioning, initiation, and/or planning (Blosser & DePompei, 2003).
Feeding and swallowing intervention aims to support safe and efficient oral intake and to ensure adequate nutrition and hydration. Age and developmental skill level at the time of injury are important considerations when designing feeding and swallowing treatment protocols and providing intervention, especially in infants and young children who can change so quickly (Mendell & Arvedson, 2016). See ASHA’s Practice Portal page on Pediatric Feeding and Swallowing.
Clinicians also consider the child’s cognitive-communication skills, oral–motor function, physical and sensory–perceptual limitations, behavioral deficits, and environmental supports in targeting dysphagia (Morgan, 2010; Morgan et al., 2002, 2004).
For further information, please see Glisson et al. (2026).
Hearing and balance intervention addresses changes in hearing and balance post-injury. Such changes can potentially exacerbate other TBI effects, especially cognitive–linguistic and social communication deficits.
Treatment for hearing loss may include selection and fitting of amplification or implantable devices and training in the use of assistive technologies (e.g., frequency modulation [FM] systems in classrooms). Hearing aids, cognitive–behavioral interventions, and/or sound masking may be used to manage tinnitus associated with TBI.
Vestibular rehabilitation programs aim to improve symptoms of vertigo and other balance-related problems following TBI (Teasell et al., 2013). Intervention may differ when balance and dizziness symptoms are due to post-concussion syndrome versus peripheral vestibular dysfunction; differential diagnosis is key to management and recovery (Doettl, 2015).
Treatment for auditory-related symptoms may also incorporate counseling regarding the use of coping and compensatory skills to minimize the effects of hearing and balance disorders and reduce safety risks.
See ASHA’s Practice Portal pages on Balance System Disorders, Tinnitus and Hyperacusis, Classroom Acoustics, Hearing Loss in Children, and Hearing Loss in Adults.
Culture and language influence how a child communicates, learns, and interacts, and cultural and linguistic norms vary greatly from family to family. Effective treatment plans take these variables into account to help the child function best in their environment. Family beliefs, preferences, and access to resources help determine priorities in treatment, support authentic participation, and strengthen collaboration with caregivers.
Treatment is completed in the language(s) used by the individual with TBI and their caregivers, including counseling, education, and any written materials shared. See ASHA’s page on Social Determinants of Health and Practice Portal pages on Multilingual Service Delivery in Audiology and Speech-Language Pathology; Cultural Responsiveness; and Collaborating With Interpreters, Transliterators, and Translators).
Preschoolers do not have a consistent point of entry into educational support systems following the acute stages of TBI. Children may receive services through early intervention programs, outpatient rehabilitation, or other community-based services depending on eligibility and local resources. Early intervention services are ideally provided in natural environments and emphasize family-centered care that addresses the needs of the child and their siblings and caregivers.
Intervention for young children focuses on maintaining development and building skills needed for participation in home, community, and future educational settings. The effects of TBI may not become apparent until developmental demands increase. Therefore, ongoing monitoring of communication, cognition, behavior, and social participation is critical throughout early childhood (Ciccia et al., 2019).
Clinicians consider the child’s developmental stage, pre-injury functioning, and family priorities when establishing treatment goals. The impact of TBI on a developing brain may differ from that of developmental disorders and may affect the rate at which new skills are acquired (Agrawal et al., 2026).
Families and professionals should communicate the child’s history of TBI to educational teams as children approach school entry and progress through new educational environments. Ongoing collaboration among health care providers, families, early childhood programs, and schools can help identify emerging difficulties and ensure timely supports as academic, social, and behavioral expectations increase (Dichiaro et al., 2023; Haarbauer-Krupa et al., 2023).
Most children with TBI attend school or will attend school. As a result, treatment by a SLP often focuses on the educational environment. Children with TBI may demonstrate needs in areas such as language, cognitive-communication, pragmatics, executive functioning, social competence, behavior, and participation. School-based supports may need to be individualized based on the student’s profile and social and environmental contexts (Crook et al., 2023; Riccardi et al., 2022).
Children with TBI may qualify for special education and related services through
School teams consider the student’s educational performance; functional communication; cognitive-communication needs; participation in academic and social routines; and need for accommodations, modifications, assistive technology, or specialized instruction.
Students with TBI may not be identified or supported immediately because symptoms can change over time. Additional needs may emerge as academic and social demands increase. “Hospital-to-school transition services, educational supports and services, and long-term follow-up must be individualized for students with acquired brain injury (ABI)” (Riccardi et al., 2021).
SLPs help facilitate communication among caregivers, medical providers, rehabilitation professionals, educators, and school teams. This collaboration can help identify students with TBI, contribute to the development of appropriate school reentry plans, and provide for ongoing monitoring of skills (Perrier et al., 2026). SLPs also educate caregivers, teachers, and other school personnel about
Collaboration among specialized instructional support personnel (e.g., physical therapists, SLPs) and the child, their caregivers, school staff, and other relevant partners will help manage difficulties and provide accommodations.
Organizing a systematic return to school is central to supporting the student’s academic and social participation. Return-to-school programs may be housed in health care settings, schools, or state agencies. Program structures differ in access, models of care, and how students are monitored over time. Children with TBI benefit from health care assessment and follow-up that includes parental involvement when returning to school (Haarbauer-Krupa et al., 2023).
Youth with persistent deficits following TBI may continue to experience difficulties as they transition to other settings (e.g., postsecondary education, employment, independent living). Because the effects of childhood TBI can evolve as developmental and environmental demands increase, ongoing monitoring and individualized supports may be needed throughout adolescence and young adulthood. School- and community-based supports are ideally tailored to the individual’s strengths, needs, and future goals (Riccardi et al., 2021).
SLPs collaborate with multiple partners, including the individual, their families, educational teams, vocational personnel, and others to facilitate successful transitions to adulthood.
See ASHA’s resource on postsecondary transition planning and Riccardi et al. (2021).
Students with TBI may experience persistent deficits that can affect success in postsecondary education, vocational training, employment, and independent living. Ongoing assessment that considers communication, participation, and contextual factors can help identify supports needed to promote successful transition outcomes.
Transition planning may include connecting students and families with supports (e.g., community resources, disability support services) before graduation from high school. Students with acquired brain injury may require individualized educational supports and long-term follow-up because needs can change over time as academic, vocational, and social demands increase (Riccardi et al., 2021).
School and community professionals collaborate to identify accommodations and supports that facilitate participation and learning. Depending on the student’s needs and setting, accommodations may include extended time for testing and assignments; modified course schedules; and assistive technologies that support reading, writing, organization, and communication (Riccardi et al., 2021).
SLPs may support students transitioning to postsecondary education through
Youth with TBI experience unique challenges in postsecondary community and/or work environments. Fatigue and sensory issues as well as deficits in oral communication, pragmatic language, literacy, attention, and memory are among the factors that may negatively affect independent living and performance in social and professional settings.
The SLP identifies current cognitive-communication deficits, determines how these may affect life skills and job performance, and then teaches the individual strategies that can help minimize the impact of the deficits in functional settings (Bonelli et al., 2007). The SLP collaborates with a vocational rehabilitation therapist as appropriate, assessing and treating functional work and community-based skills in context and implementing the necessary accommodations for maximum outcomes.
Format refers to the structure of the treatment session (e.g., group and/or individual; direct and/or pullout; integrated and/or consultative). The appropriateness of the treatment format often depends on the service delivery setting, stage of recovery, severity of injury, and primary goal at a particular point in the intervention process.
Formats in acute care or rehabilitation hospitals will look much different from those that are school or community based. For example, initial treatment may involve one-on-one strategy training and/or practice in using AAC with family members only. However, once the child has made progress on these goals, group treatment may be considered to provide opportunities for generalization and practice.
Group therapy can also target cognitive domains and provide opportunities to initiate social interactions and engage in project-based learning in structured and natural environments with feedback from the clinician and peers (Hickey & Saunders, 2010; Teasell et al., 2013).
Telepractice may be another appropriate avenue of service delivery. Telepractice can focus on improving the child’s functional abilities while offering support and training to caregivers, teachers, and employers in functional everyday environments. Telepractice eliminates the need to travel and can facilitate practice, carryover, and generalization of skills in naturalistic contexts (Houston, 2013; Rietdijk et al., 2012; Turkstra et al., 2012). It may also reduce barriers related to geography or the limited number of service providers in a family’s area with professional experience related to pediatric TBI. See ASHA’s Practice Portal page on Telepractice.
Provider refers to the person providing treatment (e.g., SLP, trained volunteer, caregiver, or teacher). Recommended practices follow a collaborative process that involves an interdisciplinary team including the child, family, caregivers, and professionals. Family, teachers, and significant others play a critical role in supporting and augmenting the treatment plan. When rehabilitation incorporates accommodations, modifications, and supports in everyday settings, SLPs often provide (a) information to help communication partners understand the child’s needs and (b) training in how to use strategies to facilitate communication. Other professionals (e.g., physical therapists or occupational therapists) may also be involved in co-treatment of deficits. See ASHA’s resources on focusing care on individuals and their care partners and collaboration and teaming.
Dosage refers to the frequency, intensity, and duration of service. Dosage depends on individual factors, including the child’s arousal level and ability to tolerate therapy sessions, prognosis, stage in recovery, and frequency of other therapeutic activity (CDC, 2015).
Setting refers to the location of treatment and varies across the continuum of care (e.g., acute care or rehabilitation hospital, home, school- or community-based).
Following time in acute care hospital and rehabilitation settings, young children with TBI return home to receive services through early intervention, preschool, or community-based programs. Older children return to school, where long-term rehabilitation services are provided (Haarbauer-Krupa, 2012a, 2012b). The role of the SLP in the transition from hospital settings to school settings is key in identifying students who qualify for services and helping them access these services and any other necessary educational supports (Allison et al., 2017; Allison & Turkstra, 2012; Denslow et al., 2012; Glang et al., 2008; Haarbauer-Krupa, 2012b; Savage et al., 2001).
This list of resources is not exhaustive, and the inclusion of any specific resource does not imply endorsement from ASHA.
Agrawal, S., Mannix, R., Anderson, V., Beauchamp, M. H., Ferguson, A., Braga, L. W., Chong, S.-L., Figaji, A., Giza, C., Menon, D. K., & Bell, M. J. (2026). Paediatric traumatic brain injury: Unique population and unique challenges. Brain, 149(3), 736–756. https://doi.org/10.1093/brain/awaf459
Alessi, L. J., MacCarthy, M., McCormick, A., Edinger, J., Houtrow, A. J., Simon, D. W., Gaines, B. A., Horvat, C. M., & Fink, E. L. (2026). Multidisciplinary rehabilitation and follow-up for children hospitalized with traumatic brain injury. Journal of Pediatric Rehabilitation Medicine, 19(1), 75–85. https://doi.org/10.1177/18758894241312482
Allison, K. M., Byom, L. J., & Turkstra, L. S. (2017). Traumatic brain injury in children and adolescents. In A. Johnson & B. Jacobson (Eds.), Medical speech-language pathology (3rd ed., pp. 103–118). Thieme.
Allison, K. M., & Turkstra, L. S. (2012). Navigating medical speech-language pathology reports for children with TBI. Perspectives on School-Based Issues, 13(3), 63–69. https://doi.org/10.1044/sbi13.3.63
Allonsius, F., de Kloet, A. J., van Markus-Doornbosch, F., Vliet Vlieland, T. P. M., & van der Holst, M. (2024). A longitudinal follow-up study of parent-reported family impact and quality of life in young patients with traumatic and non-traumatic brain injury. Disability and Rehabilitation, 46(11), 2240–2250. https://doi.org/10.1080/09638288.2023.2218657
American Psychiatric Association. (2022). Diagnostic and statistical manual of mental disorders (5th ed., text revision)
American Speech-Language-Hearing Association. (2003). Rehabilitation of children and adults with cognitive-communication disorders after brain injury [Technical report]. https://www.asha.org/policy/
American Speech-Language-Hearing Association. (2016). Scope of practice in speech-language pathology [Scope of practice]. https://www.asha.org/policy/
American Speech-Language-Hearing Association. (2018). Scope of practice in audiology [Scope of practice]. https://www.asha.org/policy/
American Speech-Language-Hearing Association. (2023). Code of ethics [Ethics]. https://www.asha.org/policy/
Anderson, V., Catroppa, C., Morse, S., Haritou, F., & Rosenfeld, J. (2005). Functional plasticity or vulnerability after early brain injury? Pediatrics, 116(6), 1374–1382. https://doi.org/10.1542/peds.2004-1728
Anderson, V., Godfrey, C., Rosenfeld, J. V., & Catroppa, C. (2012). Predictors of cognitive function and recovery 10 years after traumatic brain injury in young children. Pediatrics, 129(2), e254–e261. https://doi.org/10.1542/peds.2011-0311
Baticulon, R. E., Sy, J. J., Haizel-Cobbina, J., Du, L., Figueredo, L., Hounjet, C., Mitchell, R., Shlobin, N. A., & Dewan, M. C. (2026). Global epidemiology of pediatric traumatic brain injury: Systematic review and meta-analysis. Neurosurgery, 99(3), 496–509. https://doi.org/10.1227/neu.0000000000003875
Beauchamp, M. H., Anderson, V., Ewing-Cobbs, L., Haarbauer-Krupa, J., McKinlay, A., Wade, S. L., & Suskauer, S. J. (2024). Early childhood concussion. Pediatrics, 154(5), Article e2023065484. https://doi.org/10.1542/peds.2023-065484
Black, L. I., & Zablotsky, B. (2021, December 1). Concussions and brain injuries in children: United States, 2020. NCHS Data Brief No. 423, 1–8. https://doi.org/10.15620/cdc:111174
Blosser, J. L., & DePompei, R. (2003). Pediatric traumatic brain injury: Proactive intervention. Delmar.
Bonelli, P., Ritter, P., & Kinsler, E. (2007, November). The speech-language pathologist’s role in vocational outcomes [Poster presentation]. Annual Convention of the American Speech-Language-Hearing Association, Boston, MA, United States.
Burns, M. S. (2004). Speech-language pathology management of TBI in school-aged children. Perspectives on School-Based Issues, 5(3), 14–19. https://doi.org/10.1044/sbi5.3.14
CARF International. (2015). Medical rehabilitation program list. https://carf.org/accreditation/programs/medical-rehabilitation/medical-rehabilitation-program-list/
Catroppa, C., & Anderson, V. (2009). Neurodevelopmental outcomes of pediatric traumatic brain injury. Future Neurology, 4(6), 811–821. https://doi.org/10.2217/fnl.09.52
Centers for Disease Control and Prevention. (2015). Report to Congress on traumatic brain injury in the United States: Epidemiology and rehabilitation. https://www.cdc.gov/traumaticbraininjury/pdf/TBI_Report_to_Congress_Epi_and_Rehab-a.pdf
Centers for Disease Control and Prevention. (2018). CDC Pediatric Mild Traumatic Brain Injury (mTBI) guideline: Management and treatment recommendations. https://www.cdc.gov/traumatic-brain-injury/media/pdfs/2018-mTBI_AtAGlance_Treatment-508.pdf [PDF]
Chevignard, M. P., Soo, C., Galvin, J., Catroppa, C., & Eren, S. (2012). Ecological assessment of cognitive functions in children with acquired brain injury: A systematic review. Brain Injury, 26(9), 1033–1057. https://doi.org/10.3109/02699052.2012.666366
Childers, C., & Hux, K. (2013). Environmental accommodations for a child with traumatic brain injury. Brain Injury, 27(7–8), 850–861. https://doi.org/10.3109/02699052.2013.775498
Ciccia, A. H., Lundine, J. P., & Brown, J. (2019). New mTBI guidelines for young children:
What do they mean? The ASHA Leader, 24(8), 40–42. https://doi.org/10.1044/leader.OTP.24082019.40
Coelho, C., Ylvisaker, M., & Turkstra, L. S. (2005). Nonstandardized assessment approaches for individuals with traumatic brain injuries. Seminars in Speech and Language, 26(4), 223–241. https://doi.org/10.1055/s-2005-922102
Cook, L. G., DePompei, R., & Chapman, S. B. (2011). Cognitive communicative challenges in TBI: Assessment and intervention in the long term. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 21(1), 33–42. https://doi.org/10.1044/nnsld21.1.33
Cox, D. M. (2016). Pediatric abusive head trauma. Wild Iris Medical Education. http://www.nursingceu.com/courses/514/index_nceu.html
Crook, L., Riccardi, J. S., Ruddock, H. S., & Ciccia, A. (2023). Speech-language pathology treatment of cognitive-communication deficits in school-aged children with traumatic brain injury: A scoping review. Journal of Speech, Language, and Hearing Research, 66(5), 1826–1841. https://doi.org/10.1044/2023_JSLHR-22-0041
Daugherty, J., Peterson, A., Black, L., & Waltzman, D. (2025). Summary of the Centers for Disease Control and Prevention’s self-reported traumatic brain injury survey efforts. The Journal of Head Trauma Rehabilitation, 40(1), E1–E12. https://doi.org/10.1097/HTR.0000000000000975
Daugherty, J., Yuan, K., Sarmiento, K., & Law, R. (2024). Are there seasonal patterns for emergency department visits for head injuries in the USA? Findings from the National Electronic Injury Surveillance System-All Injury Program. Injury Prevention, 30(1), 46–52. https://doi.org/10.1136/ip-2023-044971
Denslow, P., Doster, J., King, K., & Rayman, J. (2012). Project BRAIN: Working together to improve educational outcomes for students with traumatic brain injury. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 22(3), 106–118. https://doi.org/10.1044/nnsld22.3.106
DePompei, R. (2010, November). Pediatric traumatic brain injury: Where do we go from here? The ASHA Leader, 15(13), 16–20. https://doi.org/10.1044/leader.FTR2.15132010.16
DePompei, R., Gillette, Y., Goetz, E., Xenopoulos-Oddsson, A., Bryen, D., & Dowds, M. (2008). Practical applications for use of PDAs and smartphones with children and adolescents who have traumatic brain injury. NeuroRehabilitation, 23(6), 487–499. https://doi.org/10.3233/NRE-2008-23605
Dichiaro, M., Baker, D., & Tlustos, S. J. (2023). Return to learn after traumatic brain injury. Pediatric Clinics of North America, 70(3), 445–460. https://doi.org/10.1016/j.pcl.2023.01.004
Doettl, S. M. (2015). Sports concussions (TBI), imbalance, and dizziness. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 25(1), 36–41. https://doi.org/10.1044/nnsld25.1.36
Doyle, M., & Fager, S. (2011, February). Traumatic brain injury and AAC: Supporting communication through recovery. The ASHA Leader, 16(2). Online-only. https://doi.org/10.1044/leader.FTR8.16022011.n
Dupont, D., Beaudoin, C., Désiré, N., Tran, M., Gagnon, I., & Beauchamp, M. H. (2022, March/April). Report of Early Childhood Traumatic Injury Observations & Symptoms: Preliminary validation of an observational measure of postconcussive symptoms. The Journal of Head Trauma Rehabilitation, 37(2), E102–E112. https://doi.org/10.1097/HTR.0000000000000691
Dupont, D., Tang, K., Beaudoin, C., Dégeilh, F., Gagnon, I., Yeates, K. O., Rose, S. C., Gravel, J., Burstein, B., Stang, A. S., Stanley, R. M., Zemek, R. L., & Beauchamp, M. H. (2024). Postconcussive symptoms after early childhood concussion. JAMA Network Open, 7(3), Article e243182. https://doi.org/10.1001/jamanetworkopen.2024.3182
Ewing-Cobbs, L., & Barnes, M. (2002). Linguistic outcomes following traumatic brain injury in children. Seminars in Pediatric Neurology, 9(3), 209–217. https://doi.org/10.1053/spen.2002.35502
Ewing-Cobbs, L., Cox, C. S., Jr., Clark, A. E., Holubkov, R., & Keenan, H. T. (2018). Persistent postconcussion symptoms after injury. Pediatrics, 142(5), Article e20180939. https://doi.org/10.1542/peds.2018-0939
Fager, S., & Spellman, C. (2010). Augmentative and alternative communication intervention in children with traumatic brain injury and spinal cord injury. Journal of Pediatric Rehabilitation Medicine, 3(4), 269–277. https://doi.org/10.3233/PRM-2010-0142
Faul, M., Xu, L., Wald, M. M., & Coronado, V. G. (2010). Traumatic brain injury in the United States: Emergency department visits, hospitalizations, and deaths, 2002–2006 [CDC-INFO Pub ID 211298]. Centers for Disease Control and Prevention. https://stacks.cdc.gov/view/cdc/5571
Feeney, T. J., & Ylvisaker, M. (2008). Context-sensitive cognitive-behavioral supports for young children with traumatic brain injury: A second replication study. Journal of Positive Behavior Interventions, 10(2), 115–128. https://doi.org/10.1177/109830070731254
Gamino, J. F., Chapman, S. B., & Cook, L. G. (2009). Strategic learning in youth with traumatic brain injury: Evidence for stall in higher-order cognition. Topics in Language Disorders, 29(3), 224–235. https://doi.org/10.1097/TLD.0b013e3181b531da
Gan, C., DePompei, R., & Lash, M. (2013). Family assessment and intervention. In N. D. Zasler, D. I. Katz, & R. D. Zafonte (Eds.), Brain injury medicine: Principles and practice (pp. 621–634). Demos Medical Publishing.
Giacino, J. T., Katz, D. I., Schiff, N. D., Whyte, J., Ashman, E. J., Ashwal, S., Barbano, R., Hammond, F. M., Laureys, S., Ling, G. S. F., Nakase-Richardson, R., Seel, R. T., Yablon, S., Getchius, T. S. D., Gronseth, G. S., & Armstrong, M. J. (2018, August 8). Practice guideline update recommendations summary: Disorders of consciousness [Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology; the American Congress of Rehabilitation Medicine; and the National Institute on Disability, Independent Living, and Rehabilitation Research]. Neurology, 91(10), 450–460. https://doi.org/10.1212/WNL.0000000000005926
Glang, A., Todis, B., Thomas, C. W., Hood, D., Bedell, G., & Cockrell, J. (2008). Return to school following childhood TBI: Who gets services? NeuroRehabilitation, 23(6), 477–486. https://doi.org/10.3233/NRE-2008-23604
Glisson, E., Smith, M., Pagnamenta, E., & Pontikas, G. (2026, June 23). Dysphagia in paediatric acquired brain injury: Prevalence, outcomes, and impact of lesion sites on recovery. Developmental Medicine & Child Neurology. Advance online publication. https://doi.org/10.1111/dmcn.70382
Grant, M., & Ponsford, J. (2014). Goal Attainment Scaling in brain injury rehabilitation: Strengths, limitations and recommendations for future applications. Neuropsychological Rehabilitation, 24(5), 661–677. https://doi.org/10.1080/09602011.2014.901228
Haarbauer-Krupa, J. (2012a, July). Schools as TBI service providers. The ASHA Leader, 17(8), 10–13. https://doi.org/10.1044/leader.FTR1.17082012.10
Haarbauer-Krupa, J. (2012b). Taking care of children after traumatic brain injury. Perspectives on School-Based Issues, 13(3), 79–86. https://doi.org/10.1044/sbi13.3.79
Haarbauer-Krupa, J., & Brink, M. (2020). Taking care of preschool children who experience traumatic brain injury. Perspectives of the ASHA Special Interest Groups, 5(1), 81–87. https://doi.org/10.1044/2019_PERSP-19-00087
Haarbauer-Krupa, J., Ciccia, A., Dodd, J., Ettel, D., Kurowski, B., Lumba-Brown, A., & Suskauer, S. (2017). Service delivery in the healthcare and educational systems for children following traumatic brain injury: Gaps in care. The Journal of Head Trauma Rehabilitation, 32(6), 367–377. https://doi.org/10.1097/HTR.0000000000000301
Haarbauer-Krupa, J., Thigpen, S., Glang, A., Eagan-Johnson, B., McAvoy, K., Brunken, C., Chininis, M., Kurowski, B. G., Suskauer, S., Crowley, M., & Denslow, P. (2023). Return to school after traumatic brain injury: Description of implementation settings. The Journal of Head Trauma Rehabilitation, 38(4), 329–335. https://doi.org/10.1097/HTR.0000000000000859
Haarbauer-Krupa, J., Wray, A. P., Lebrun-Harris, L. A., Cree, R. A., & Womack, L. S. (2024). Prevalence and correlates of suspected and diagnosed traumatic brain injuries among US school-aged children. The Journal of Pediatrics: Clinical Practice, 14, Article 200117. https://doi.org/10.1016/j.jpedcp.2024.200117
Hall, A., Lundine, J. P., & McCauley, R. J. (2021). Nonstandardized assessment of cognitive-communication abilities following pediatric traumatic brain injury: A scoping review. American Journal of Speech-Language Pathology, 30(5), 2296–2317. https://doi.org/10.1044/2021_AJSLP-20-00231
Hickey, E. M., & Saunders, J. N. (2010). Group intervention for adolescents with chronic acquired brain injury: The future zone. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 20(4), 111–119. https://doi.org/10.1044/nnsld20.4.111
Hotz, G. A., Castelblanco, A., Lara, I. M., Weiss, A. D., Duncan, R., & Kuluz, J. W. (2006). Snoezelen: A controlled multi-sensory stimulation therapy for children recovering from severe brain injury. Brain Injury, 20(8), 879–888. https://doi.org/10.1080/02699050600832635
Houston, K. T. (2013). Telepractice in speech-language pathology. Plural.
Individuals with Disabilities Education Act, Pub. L. No. 108-446, 118 Stat. 2647 (2004). https://sites.ed.gov/idea/statuteregulations/
James, H. E. (1986). Neurologic evaluation and support in the child with an acute brain insult. Pediatric Annals, 15(1), 16–22. https://doi.org/10.3928/0090-4481-19860101-05
Jenkin, T., Anderson, V. A., D’Cruz, K., Scheinberg, A., & Knight, S. (2022). Family-centered service in paediatric acquired brain injury rehabilitation: Bridging the gaps. Frontiers in Rehabilitation Sciences, 3, Article 1085967. https://doi.org/10.3389/fresc.2022.1085967
Jenkin, T., D’Cruz, K., Botchway, E., Muscara, F., Anderson, V., Scheinberg, A., & Knight, S. (2025). Family involvement in rehabilitation programmes for children and adolescents with acquired brain injury: A scoping literature review. Neuropsychological Rehabilitation, 35(1), 159–212. https://doi.org/10.1080/09602011.2024.2330141
Kaschel, R., Sala, S. D., Cantagallo, A., Fahlböck, A., Laaksonen, R., & Kazen, M. (2002). Imagery mnemonics for the rehabilitation of memory: A randomised group controlled trial. Neuropsychological Rehabilitation, 12(2), 127–153. https://doi.org/10.1080/09602010143000211
Kennedy, M. (2006, October). Managing memory and metamemory impairments in individuals with traumatic brain injury. The ASHA Leader, 11(14), 8–36. https://doi.org/10.1044/leader.FTR2.11142006.8
Kennedy, M. R. T., & Coelho, C. (2005, November). Self-regulation after traumatic brain injury: A framework for intervention of memory and problem solving. Seminars in Speech and Language, 26(4), 242–255. https://doi.org/10.1055/s-2005-922103
Kingery, K. M., Narad, M. E., Taylor, H. G., Yeates, K. O., Stancin, T., & Wade, S. L. (2017). Do children who sustain traumatic brain injury in early childhood need and receive academic services 7 years after injury? Journal of Developmental & Behavioral Pediatrics, 38(9), 728–735. https://doi.org/10.1097/DBP.0000000000000489
Kiresuk, T. J., Smith, A., & Cardillo, J. E. (Eds.). (2014). Goal Attainment Scaling: Applications, theory, and measurement. Psychology Press.
Koole, H., Nelson, N. W., & Curtis, A. B. (2015). Factors influencing choices of contextualized versus traditional practices with children and adolescents who have traumatic brain injury. Language, Speech, and Hearing Services in Schools, 46(4), 352–361. https://doi.org/10.1044/2015_LSHSS-14-0109
Laatsch, L., Dodd, J., Brown, T., Ciccia, A., Connor, F., Davis, K., Doherty, M., Linden, M., Locascio, G., Lundine, J., Murphy, S., Nagele, D., Niemeier, J., Politis, A., Rode, C., Slomine, B., Smetana, R., & Yaeger, L. (2020). Evidence-based systematic review of cognitive rehabilitation, emotional, and family treatment studies for children with acquired brain injury literature: From 2006 to 2017. Neuropsychological Rehabilitation, 30(1), 130–161. https://doi.org/10.1080/09602011.2019.1678490
Lee, J., Harn, B., Sohlberg, M. M., & Wade, S. L. (2012). An overview of the Attention Improvement Management (AIM) program with outcomes for three pilot participants. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 22(3), 90–105. https://doi.org/10.1044/nnsld22.3.90
Lu, V. M., & Niazi, T. N. (2023). Epidemiology of pediatric sports-related concussions presenting to the emergency room over the last decade in the United States. Clinical Neurology and Neurosurgery, 235, Article 108023. https://doi.org/10.1016/j.clineuro.2023.108023
Lumba-Brown, A., Yeates, K. O., Sarmiento, K., Breiding, M. J., Haegerich, T. M., Gioia, G. A., Turner, M., Benzel, E. C., Suskauer, S. J., Giza, C. C., Joseph, M., Broomand, C., Weissman, B., Gordon, W., Wright, D. W., Scolaro Moser, R., McAvoy, K., Ewing-Cobbs, L., Duhaime, A.-C., . . . Timmons, S. D. (2020). Centers for Disease Control and Prevention guidelines on the diagnosis and management of mild traumatic brain injury among children. JAMA Pediatrics, 72(11), Article e182853. https://doi.org/10.1001/jamapediatrics.2018.2853
Lundine, J. P., Ciccia, A. H., & Brown, J. (2019). The speech-language pathologists’ role in mild traumatic brain injury for early childhood–, preschool–, and elementary school–age children: Viewpoints on guidelines from the Centers for Disease Control and Prevention. American Journal of Speech-Language Pathology, 28(3), 1371–1376. https://doi.org/10.1044/2019_AJSLP-18-0295
Lundine, J. P., & Hall, A. (2020). Using nonstandardized assessments to evaluate cognitive-communication abilities following pediatric traumatic brain injury. Seminars in Speech and Language, 41(2), 170–182. https://doi.org/10.1055/s-0040-1701685
Lundine, J. P., Utz, M., Jacob, V., & Ciccia, A. H. (2019). Putting the person in person-centered care: Stakeholder experiences in pediatric traumatic brain injury. Journal of Pediatric Rehabilitation Medicine, 12(1), 21–35. https://doi.org/10.3233/PRM-180568
Lundine, J. P., Viola, N., Koterba, C., & Ciccia, A. (2026). “Brain injuries affect everything”: Long-term caregiver perspectives on medical and educational needs following inpatient rehabilitation for pediatric TBI. Behavioral Sciences, 16(7), Article 1122. https://doi.org/10.3390/bs16071122
MacDonald, S., & Wiseman-Hakes, C. (2010). Knowledge translation in ABI rehabilitation: A model for consolidating and applying the evidence for cognitive-communication interventions. Brain Injury, 24(3), 486–508. https://doi.org/10.3109/02699050903518118
Manley, G. T., Dams-O’Connor, K., Alosco, M. L., Awwad, H. O., Bazarian, J. J., Bragge, P., Corrigan, J. D., Doperalski, A., Ferguson, A. R., Mac Donald, C. L., Menon, D. K., McNett, M. M., van der Naalt, J., Nelson, L. D., Pisică, D., Silverberg, N. D., Umoh, N., Wilson, L., Yuh, E. L., . . . McCrea, M. A. (2025). A new characterisation of acute traumatic brain injury: The NIH-NINDS TBI Classification and Nomenclature Initiative. The Lancet Neurology, 24(6), 512–523. https://doi.org/10.1016/S1474-4422(25)00154-1
Marshall S., Lithopoulos A., Curran D., Fischer L., Velikonja D., & Bayley, M. (2023). Living concussion guidelines: Guideline for concussion & prolonged symptoms for adults 18 years of age or older. Ontario Neurotrauma Foundation. https://concussionsontario.org
Masel, B. E., & DeWitt, D. S. (2010). Traumatic brain injury: A disease process, not an event. Journal of Neurotrauma, 27(8), 1529–1540. https://doi.org/10.1089/neu.2010.1358
Max, J. E., Troyer, E. A., Arif, H., Vaida, F., Wilde, E. A., Bigler, E. D., Hesselink, J. R., Yang, T. T., Tymofiyeva, O., Wade, O., & Paulsen, J. S. (2022). Traumatic brain injury in children and adolescents: Psychiatric disorders 24 years later. The Journal of Neuropsychiatry and Clinical Neurosciences, 34(1), 60–67. https://doi.org/10.1176/appi.neuropsych.20050104
McCart, M., Unruh, D., Gomez, D., Anderson, D., Gioia, G., Davies, S. C., Haarbauer-Krupa, J., Womack, L. S., Thigpen, S., Brown, L., & Glang, A. (2023). Using guided credible history interviews to establish special education eligibility for students with traumatic brain injury. NeuroRehabilitation, 52(4), 597–604. https://doi.org/10.3233/NRE-220211
McCrory, P., Meeuwisse, W. H., Aubry, M., Cantu, B., Dvořák, J., Echemendia, R. J., Engebretsen, L., Johnston, K., Kutcher, J. S., Raftery, M., Sills, A., Benson, B. W., Davis, G. A., Ellenbogen, R. G., Guskiewicz, K., Herring, S. A., Iverson, G. L., Jordan, B. D., Kissick, J., . . . Turner, M. (2013). Consensus statement on concussion in sport: The 4th International Conference on Concussion in Sport held in Zurich, November 2012. British Journal of Sports Medicine, 47(5), 250–258. https://doi.org/10.1136/bjsports-2013-092313
McDonald, S., Togher, L., & Code, C. (Eds.). (2014). Social and communication disorders following traumatic brain injury. Psychology Press.
McKinlay, A., & Anderson, V. (2013, October). Issues associated with pre-school child traumatic brain injury. In World Health Organization & International Brain Injury Association (Eds.), International NeuroTrauma Letter, 33, Article 259591479. HDI Publishers.
Mendell, D. A., & Arvedson, J. C. (2016). Dysphagia in pediatric traumatic brain injury. Current Physical Medicine and Rehabilitation Reports, 4, 233–236. https://doi.org/10.1007/s40141-016-0132-7
Mesfin, F. B., Gupta, N., Hays Shapshak, A., & Margetis, K. (2025). Diffuse axonal injury. StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK448102/
Morgan, A. T. (2010). Dysphagia in childhood traumatic brain injury: A reflection on the evidence and its implications for practice. Developmental Neurorehabilitation, 13(3), 192–203. https://doi.org/10.3109/17518420903289535
Morgan, A. T., Mageandran, S.-D., & Mei, C. (2010). Incidence and clinical presentation of dysarthria and dysphagia in the acute setting following paediatric traumatic brain injury. Child: Care, Health and Development, 36(1), 44–53. https://doi.org/10.1111/j.1365-2214.2009.00961.x
Morgan, A. T., & Vogel, A. P. (2008). Intervention for dysarthria associated with acquired brain injury in children and adolescents. Cochrane Database of Systematic Reviews, 2008(3), Article CD006279. https://doi.org/10.1002/14651858.CD006279.pub2
Morgan, A., Ward, E., & Murdoch, B. (2004). Clinical progression and outcome of dysphagia following paediatric traumatic brain injury: A prospective study. Brain Injury, 18(4), 359–376. https://doi.org/10.1080/02699050310001617424
Morgan, A., Ward, E., Murdoch, B., & Bilbie, K. (2002). Acute characteristics of pediatric dysphagia subsequent to traumatic brain injury: Videofluoroscopic assessment. The Journal of Head Trauma Rehabilitation, 17(3), 220–241. https://doi.org/10.1097/00001199-200206000-00004
Morgan, A., Ward, E., Murdoch, B., Kennedy, B., & Murison, R. (2003). Incidence, characteristics, and predictive factors for dysphagia after pediatric traumatic brain injury. The Journal of Head Trauma Rehabilitation, 18(3), 239–251. https://doi.org/10.1097/00001199-200305000-00002
Munakomi, S., Margetis, K., & Iverson, L. M. (2026). Glasgow Coma Scale. StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK513298/
National Institutes of Health. (1998). Rehabilitation of persons with traumatic brain injury [NIH consensus statement].
New York State Education Department. (2002). Traumatic brain injury: A guidebook for educators.
New Zealand Guidelines Group. (2006). Traumatic brain injury: Diagnosis, acute management and rehabilitation.
Oberg, L., & Turkstra, L. S. (1998). Use of elaborative encoding to facilitate verbal learning after adolescent traumatic brain injury. The Journal of Head Trauma Rehabilitation, 13(3), 44–62. https://doi.org/10.1097/00001199-199806000-00005
OʼNeil-Pirozzi, T. M., Kennedy, M. R. T., & Sohlberg, M. M. (2015). Evidence-based practice for the use of internal strategies as a memory compensation technique after brain injury: A systematic review. The Journal of Head Trauma Rehabilitation, 31(4), E1–E11. https://doi.org/10.1097/HTR.0000000000000181
Perrier, M.-F., Buchel, C., Nahmad, V., Townsend, T., Haarbauer-Krupa, J., & Lundine, J. P. (2026). Pediatric traumatic brain injury: Speech-language pathologists must have a seat at the table. American Journal of Speech-Language Pathology. Advance online publication. https://doi.org/10.1044/2026_AJSLP-26-00120
Peterson, A. B., Waltzman, D., Daugherty, J., Chen, J., & Breiding, M. (2024). Sport and recreation related concussion in children: National Concussion Surveillance System. American Journal of Preventive Medicine, 67(3), 370–379. https://doi.org/10.1016/j.amepre.2024.05.003
Politis, A. M., & Norman, R. S. (2016). Computer-based cognitive rehabilitation for individuals with traumatic brain injury: A systematic review. Perspectives of the ASHA Special Interest Groups,1(2), 18–46. https://doi.org/10.1044/persp1.SIG2.18
Rehabilitation Act of 1973, 29 U.S.C. § 701 et seq. (1973). https://sites.ed.gov/idea/about-idea/#Rehab-Act
Riccardi, J. S., Crook, L., Eagan-Johnson, B., Vaccaro, M., & Ciccia, A. H. (2021). Serving students with acquired brain injury: Understanding long-term need and outcomes after the BrainSTEPS program. Perspectives of the ASHA Special Interest Groups, 6(6), 1762–1775. https://doi.org/10.1044/2021_PERSP-21-00059
Riccardi, J. S., Crook, L., Oskowski, M., & Ciccia, A. (2022). Speech-language pathology assessment of school-age children with traumatic brain injury: A scoping review. Language, Speech, and Hearing Services in Schools, 53(4), 1202–1218. https://doi.org/10.1044/2022_LSHSS-22-00049
Riccardi, J. S., D’Angelo, E., Hagen, E. B., Pei, Y., Ciccia, A., Haarbauer-Krupa, J., O’Brien, K. H., & Lundine, J. P. (2025). The importance of identifying children with brain injury in schools: Speech-language pathologists as crucial partners. American Journal of Speech-Language Pathology, 34(3S), 1839–1842. https://doi.org/10.1044/2024_AJSLP-24-00107
Rietdijk, R., Togher, L., & Power, E. (2012). Supporting family members of people with traumatic brain injury using telehealth: A systematic review. Journal of Rehabilitation Medicine, 44(11), 913–921. https://doi.org/10.2340/16501977-1058
Roscigno, C. I., & Swanson, K. M. (2011). Parents’ experiences following children’s moderate to severe traumatic brain injury: A clash of cultures. Qualitative Health Research, 21(10),1413–1426. https://doi.org/10.1177/1049732311410988
Savage, R. C., Pearson, S., McDonald, H., Potoczny-Gray, A., & Marchese, N. (2001). After hospital: Working with schools and families to support the long term needs of children with brain injuries. NeuroRehabilitation, 16(1), 49–58. https://doi.org/10.3233/NRE-2001-16107
Shankar, J., Nicholas, D., Mrazik, M., Waugh, E., Tan, S., Zulla, R., Urichuk, L., & Paranica, S. (2018). Transition from pediatric to adult services: Challenges for family caregivers of young adults with traumatic brain injury. Sage Open, 8(4), Article 2158244018807954. https://doi.org/10.1177/2158244018807954
Shum, D., Fleming, J., Gill, H., Gullo, M. J., & Strong, J. (2011). A randomized controlled trial of prospective memory rehabilitation in adults with traumatic brain injury. Journal of Rehabilitation Medicine, 43(3), 216–223. https://doi.org/10.2340/16501977-0647
Silverberg, N. D., Iverson, G. L., ACRM Brain Injury Special Interest Group Mild TBI Task Force, & ACRM Mild TBI Diagnostic Criteria Expert Consensus Group. (2023). The American Congress of Rehabilitation Medicine diagnostic criteria for mild traumatic brain injury. Archives of Physical Medicine and Rehabilitation, 104(8), 1343–1355. https://doi.org/10.1016/j.apmr.2023.03.036
Silverberg, N. D., Iverson, G. L., Arciniegas, D. B., Bayley, M. T., Bazarian, J. J., Bell, K. R., Cifu, D. X., Dams-O’Connor, K., Dikmen, S. S., Graham, J. E., & Whitehair, V. (2021). Expert panel survey to update the American Congress of Rehabilitation Medicine definition of mild traumatic brain injury. Archives of Physical Medicine and Rehabilitation, 102(1), 76–86. https://doi.org/10.1016/j.apmr.2020.08.022
Slomine, B. S., & Suskauer, S. J. (2024). Disorders of consciousness in children: Assessment, treatment, and prognosis. Physical Medicine and Rehabilitation Clinics of North America, 35(1), 223–234. https://doi.org/10.1016/j.pmr.2023.06.012
Sohlberg, M. M. (2002). An overview of approaches for managing attention impairments. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 12(3), 4–8. https://doi.org/10.1044/nnsld12.3.4
Sohlberg, M. M., Avery, J., Kennedy, M., Ylvisaker, M., Coelho, C., Turkstra, L., & Yorkston, K. (2003). Practice guidelines for direct attention training. Journal of Medical Speech-Language Pathology, 11(3), xix–xxxix.
Sohlberg, M. M., Ehlhardt, L., & Kennedy, M. (2005). Instructional techniques in cognitive rehabilitation: A preliminary report. Seminars in Speech and Language, 26(4), 268–279. https://doi.org/10.1055/s-2005-922105
Sohlberg, M. M., Harn, B., MacPherson, H., & Wade, S. L. (2014). A pilot study evaluating attention and strategy training following pediatric traumatic brain injury. Clinical Practice in Pediatric Psychology, 2(3), 263–280. https://doi.org/10.1037/cpp0000072
Sohlberg, M. M., Kennedy, M. R. T., Avery, J., Coelho, C., Turkstra, L., Ylvisaker, M., & Yorkston, K. (2007). Evidence based practice for the use of external aids as a memory rehabilitation technique. Journal of Medical Speech-Language Pathology, 15(1), xv–li.
Sohlberg, M. M., & Mateer, C. A. (2001). Cognitive rehabilitation: An integrative neuropsychological approach. Guilford.
Sohlberg, M. M., & Turkstra, L. S. (2011). Optimizing cognitive rehabilitation: Effective instructional methods. Guilford.
Taylor, C. A., Bell, J. M., Breiding, M. J., & Xu, L. (2017). Traumatic brain injury–related emergency department visits, hospitalizations, and deaths—United States, 2007 and 2013. Morbidity and Mortality Weekly Report Surveillance Summaries, 66(9), 1–16. https://doi.org/10.15585/mmwr.ss6609a1
Taylor, S. J., Barker, L. A., Heavey, L., & McHale, S. (2013). The typical developmental trajectory of social and executive functions in late adolescence and early adulthood. Developmental Psychology, 49(7), 1253–1265. https://doi.org/10.1037/a0029871
Teasdale, G., Maas, A., Lecky, F., Manley, G., Stocchetti, N., & Murray, G. (2014). The Glasgow Coma Scale at 40 years: Standing the test of time. The Lancet Neurology, 13(8), 844–854. https://doi.org/10.1016/S1474-4422(14)70120-6
Teasell, R. W., Marshall, S., Cullen, N., Bayley, M., Rees, L., Weiser, M., & Aubut, J.-A. (2013). Evidence-based review of moderate to severe acquired brain injury: Executive summary. Ontario Neurotrauma Foundation.
Togher, L. (2014). Training communication partners of people with TBI: Communication really is a two way process. In S. McDonald, L. Togher, & C. Code (Eds.), Social and communication disorders following traumatic brain injury (pp. 336–360). Psychology Press.
Togher, L., McDonald, S., Tate, R., Power, E., & Rietdijk, R. (2013). Training communication partners of people with severe traumatic brain injury improves everyday conversations: A multicenter single blind clinical trial. Journal of Rehabilitation Medicine, 45(7), 637–645. https://doi.org/10.2340/16501977-1173
Togher, L., Power, E., McDonald, S., Tate, R., & Rietdijk, R. (2010). TBI Express: A communication training program for everyday communication partners of people with traumatic brain injury. ACQuiring Knowledge in Speech, Language and Hearing, 12, 82–84.
Turkstra, L. S. (1999). Language testing in adolescents with brain injury: A consideration of the CELF-3. Language, Speech, and Hearing Services in Schools, 30(2), 132–140. https://doi.org/10.1044/0161-1461.3002.132
Turkstra, L. S., Politis, A. M., & Forsyth, R. (2015). Cognitive–communication disorders in children with traumatic brain injury. Developmental Medicine & Child Neurology, 57(3), 217–222. https://doi.org/10.1111/dmcn.12600
Turkstra, L. S., Quinn-Padron, M., Johnson, J. E., Workinger, M. S., & Antoniotti, N. (2012). In-person versus telehealth assessment of discourse ability in adults with traumatic brain injury. The Journal of Head Trauma Rehabilitation, 27(6), 424–432. https://doi.org/10.1097/HTR.0b013e31823346fc
U.S. Department of Education. (n.d.). About IDEA. https://sites.ed.gov/idea/about-idea/
Valovich McLeod, T., & Guskiewicz, K. (2012). Balance testing. In M. Kirkwood & K. Yeates (Eds.), Mild traumatic brain injury in children and adolescents (pp. 218–240). Guilford.
Wade, S. L., Taylor, H. G., Yeates, K. O., Drotar, D., Stancin, T., Minich, N. M., & Schluchter, M. (2006). Long-term parental and family adaptation following pediatric brain injury. Journal of Pediatric Psychology, 31(10), 1072–1083. https://doi.org/10.1093/jpepsy/jsj077
Waltzman, D., Black, L. I., Daugherty, J., Peterson, A. B., & Zablotsky, B. (2025). Prevalence of traumatic brain injury among adults and children. Annals of Epidemiology, 103, 40–47. https://doi.org/10.1016/j.annepidem.2025.02.005
Wehman, P., Chen, C.-C., West, M., & Cifu, G. (2014). Transition planning for youth with traumatic brain injury: Findings from the National Longitudinal Transition Survey-2. NeuroRehabilitation, 34(2), 365–372. https://doi.org/10.3233/NRE-131029
Wild, M. R. (2013). Assistive technology for cognition following brain injury: Guidelines for device and app selection. Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders, 23(2), 49–58. https://doi.org/10.1044/nnsld23.2.49
Wild, M. R. (2014). Principles of app selection and training after brain injury. Perspectives on Augmentative and Alternative Communication, 23(3), 140–147. https://doi.org/10.1044/aac23.3.140
Wintrow, S. (2013). The auditory and vestibular consequences of traumatic brain injury and the role of the audiologist on the interdisciplinary management team [Unpublished capstone project]. Ohio State University.
World Health Organization. (2001). International classification of functioning, disability and health.
Ylvisaker, M. E. (1998). Traumatic brain injury rehabilitation: Children and adolescents. Butterworth-Heinemann.
Ylvisaker, M., Adelson, P. D., Braga, L. W., Burnett, S. M., Glang, A., Feeney, T., Moore, W., Rumney, P., & Todis, B. (2005). Rehabilitation and ongoing support after pediatric TBI: Twenty years of progress. The Journal of Head Trauma Rehabilitation, 20(1), 95–109. https://doi.org/10.1097/00001199-200501000-00009
Ylvisaker, M., & Feeney, T. (1998). Collaborative brain injury intervention: Positive everyday routines (1st ed.). Cengage Learning.
Ylvisaker, M., & Feeney, T. (2007). Pediatric brain injury: Social, behavioral, and communication disability. Physical Medicine and Rehabilitation Clinics of North America, 18(1), 133–144. https://doi.org/10.1016/j.pmr.2006.11.007
Ylvisaker, M., Feeney, T., & Capo, M. (2007). Long-term community supports for individuals with co-occurring disabilities after traumatic brain injury: Cost effectiveness and project-based intervention. Brain Impairment, 8(3), 276–292. https://doi.org/10.1375/brim.8.3.276
Ylvisaker, M., Turkstra, L. S., & Coelho, C. (2005). Behavioral and social interventions for individuals with traumatic brain injury: A summary of the research with clinical implications. Seminars in Speech and Language, 26(4), 256–267. https://doi.org/10.1055/s-2005-922104
Ylvisaker, M., Turkstra, L., Coelho, C., Yorkston, K., Kennedy, M., Sohlberg, M. M., & Avery, J. (2007). Behavioural interventions for children and adults with behaviour disorders after TBI: A systematic review of the evidence. Brain Injury, 21(8), 769–805. https://doi.org/10.1080/02699050701482470
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The recommended citation for this Practice Portal page is:
American Speech-Language-Hearing Association. (n.d.). Pediatric Traumatic Brain Injury [Practice portal]. Retrieved month day, year, from www.asha.org/practice-portal/clinical-topics/pediatric-traumatic-brain-injury/
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