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Brain Injuries, Traumatic1st-BIENNCT05261477

Brain Injury Education and Outpatient Navigation-1stBIEN

A study testing Bilingual Brain Injury Education and outpatient Navigation for Hispanic families in people with Brain Injuries, Traumatic and Rehabilitation, run by Seattle Children's Hospital at 6 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Traumatic brain injury (TBI) is a significant problem for U.S. Hispanic children. Compared to non-Hispanic children, Hispanic children have higher long-term disability and lower health related quality of life, even though differences are not present at hospital discharge. Read more about this study

Who is it for?
Ages 3 years and older
Conditions the study is for
Brain Injuries, Traumatic, Rehabilitation
What is being tested?
Bilingual Brain Injury Education and outpatient Navigation for Hispanic families
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
6 sitesUnited States
Study dates
7 Jul 2022to Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Child:
  • Prior neurological deficits,
  • Acquired brain injuries secondary to other conditions different from trauma.
  • Traumatic brain injuries secondary to abusive trauma.
  • Parent:
  • Loss of custody of the child (i.e. abusive head trauma)
  • Inability to be contacted by phone

Trial locations and contacts

6 sites in 1 country. Contact the study team or a site near you to ask about taking part.

6 sites in 1 country

United States6 sites, 4 recruiting
  • Children's Hospital Colorado

    Colorado Springs, Colorado, 80920

    Alison Colbert, PhD, Alison.Colbert@childrenscolorado.org

    Michael Dichiaro, MD, Mike.Dichiaro@childrenscolorado.org

    Recruiting
  • UT Southwestern Medical Center

    Dallas, Texas, 75390

    Robert Rinaldi, MD FAAPMR, 214-648-2733, Robert.Rinaldi@UTSouthwestern.edu

    Robert Rinaldi, MD

    Recruiting
  • Oregon Health & Science University

    Portland, Oregon, 97239

    Active, not recruiting
  • University of Utah

    Salt Lake City, Utah, 84112

    Withdrawn
  • Harborview Medical Center - University of Washington

    Seattle, Washington, 98104

    Maria A Oliva, MS, 206-884-2506, andrea.oliva@seattlechildrens.org

    Frederick P Rivara, MD

    Recruiting
  • Seattle Children's Hospital

    Seattle, Washington, 98105

    Maria A Oliva, MS, 206-884-2506, andrea.oliva@seattlechildrens.org

    Nathalia Jimenez, MD, MPH

    Recruiting

Other trials in United States

About this study

Official title: Brain Injury Education and Outpatient Navigation for Hispanic Children and Their Caregivers-1stBIEN

Traumatic brain injury (TBI) is a significant problem for U.S. Hispanic children. Compared to non-Hispanic children, Hispanic children have higher long-term disability and lower health related quality of life, even though differences are not present at hospital discharge. Rehabilitation decreases disability, but needs timely initiation, and long treatments in hospitals, community healthcare facilities and schools. Parents play a key role in their child's recovery. Hispanic parents face additional barriers to initiate and maintain outpatient treatments. They report knowledge gaps in TBI-education, community, and school support systems; language and health literacy barriers. The investigators developed, a bilingual bicultural theory-based program for Hispanic families consisting of Brain Injury Education and outpatient care Navigation (1st BIEN). It integrates in-person education enriched by video content delivered through mobile phones, with navigation during transitions to outpatient care and school return. The pilot established feasibility and acceptability of the program. This randomized control trial will determine efficacy to maintain long-term adherence to rehabilitation and reduce disability. It will enroll 150 parent-child dyads: children (6-17 y), with mild-complicated, moderate-severe TBI in 5 centers in Washington, Texas, Dallas, Utah and Oregon and their parents. Intervention group parents receive: One in-person education session, plus bi-weekly videos tailored to the child's TBI and therapies; and, 3-months of bilingual outpatient care navigation. Attention control parents receive one in person-education session, monthly well-child texts and usual institutional follow up care. Primary outcome is treatment adherence at 6 months post-discharge measured by percentage of follow-up appointments attended during the prescribed time at hospitals, and community care facilities. Secondary outcomes are functional status of the child using PROMIS parental report measures; and parental health literacy, self-efficacy, and mental health at 3, 6, and 12 months after discharge. Child's academic performance will be assessed using school records. The study evaluates a flexible and scalable intervention using mobile phones to aid transitions of care, improve treatment adherence and TBI outcomes. It addresses the needs of an understudied population and can serve as a model for TBI family centered care for at risk groups.

Read the detailed description

TBI is a major cause of acquired disability in children. Approximately 60% of children with moderate to severe TBI have long-term cognitive, emotional, or physical deficits. Compared to non-Hispanic children, Hispanic children have higher disability 3 years after TBI, even though differences are not present at hospital discharge. Known risk factors for poor TBI outcomes in children such as underinsurance, low socioeconomic status, and limited parental education are highly prevalent among Hispanics, especially among immigrants from Central America and Mexico. Barriers for receipt of outpatient rehabilitation for Hispanic children are multiple including gaps in understanding of TBI and treatments, limited availability of culturally and linguistically relevant educational resources; and barriers to access services due to transportation, and under-insurance.

Education and navigation programs are efficacious in improving adherence to treatment for children with chronic conditions but have not been tested in children with TBI, despite the need for long-term outpatient rehabilitation. The investigators developed and pilot tested the 1st intervention designed for Hispanic children with TBIs and their families consisting of Brain Injury Education and outpatient Navigation (1st BIEN). The 1st BIEN intervention proposes the novel use of telephone based, culturally relevant patient navigation and education for Hispanic parents of children with TBI. It aims to improve access and adherence to treatment to decrease disability in this high-risk and understudied population. In the 1st BIEN pilot, the investigators established feasibility and acceptability for the program. Now the investigators propose a multicenter randomized controlled trial to test the efficacy of 1st BIEN to maintain long-term adherence to rehabilitation and determine its effect on child's functional outcomes.

Specific aims:

Aim 1. Test the efficacy of the 1st BIEN intervention to improve receipt of overall 1 year follow-up care and outpatient rehabilitation after a TBI among children and adolescents of Hispanic families.

Hypothesis 1a. Intervention group children will have higher attendance at follow-up appointments and higher initiation and attendance at outpatient therapies 6 months after discharge, compared to control children.

Aim 2. Determine the effect of the 1st BIEN intervention on functional outcomes and social participation at 3, 6 and 12 months after TBI hospital discharge among children and adolescents of Hispanic families.

Hypothesis 2a. Intervention group children will have higher adaptive functioning, health related quality of life, better physical, and emotional function, at 3, 6 and 12 months after hospital discharge, compared to control children.

Hypothesis 2b. Intervention group children will have higher levels of social participation measured by earlier school reintegration, receipt of educational resources, and participation in extracurricular activities.

Exploratory Aim 3. Test possible moderators and mediators of 1st BIEN intervention effects. Exploratory analyses will test possible moderators of intervention effects (i.e. pre-injury parental acculturation and education) and possible mediators (i.e. post-intervention parental knowledge, self-efficacy, mental health).

Study design:

Multi-center randomized control trial, enrolling 150 parent-child dyads; Hispanic children 3-17 years of age, hospitalized with a mild, moderate or severe TBI and their primary caregiver parent from 5 centers in Washington, Texas, Dallas, Utah and Oregon. All parents will receive in person education and linguistically and culturally tailored written TBI materials. Intervention parents additionally receive 3 months of Patient Navigation (PN) to support transitions of care and video education through mobile phone devices to promote TBI advocacy skills and reinforce essential TBI knowledge. Control group parents will receive well-child texts once a month to control for attention and follow up per institutional standard of care. Control parents do not receive patient navigation or video education.

Randomization will be done in a 1:1 ratio at each participating institution using a computer-generated random assignment sequence prepared by the study biostatistician and stratified by injury severity (mild complicated; moderate-severe) and age (3-5; 6-11;12-17).

While education using the 1stBIEN booklet is not part of the current usual care at participating institutions, providing all families with initial education at the time of discharge addresses ethical and practical considerations. It standardizes discharge processes at participating institutions while delineating differences in the intensity of education and care coordination activities. The written information given to the attention control group does not equal the amount (dosage) given to the intervention group but provides consistent information to all participants.

Considering that acute processes of care can influence outpatient adherence to treatment and patient outcomes, the investigators will measure institutional and patient level quality indicators of acute rehabilitation care. At the individual level the investigators will measure receipt of inpatient physical, occupational, and speech therapy evaluations and rehabilitation consults; and indicators of family centered care such as assistance with identified needs, telephone counseling services and provision of a contact person for questions after discharge.

Reliability of the intervention will be ensured through meticulous in-person training prior to intervention implementation and monitoring of strict adherence to elements of the intervention. Education of PNs follows a pre-determined curriculum that includes screening and recruitment procedures, inform consent procedures, education of parents using the written materials and using lay language. Training on how to conduct baseline evaluations, scales and forms. After the training PNs should demonstrate proficiency in all procedures, in two case scenarios including use of problem-solving skills during follow-up patient navigation calls, delivery of initial education and delivery of individualized video content education. These tasks will also be monitored on a regular basis via weekly conference calls and complemented by site visits once a year. the investigators will audit twenty percent of PN calls to check for protocol adherence using a standardized checklist. the investigators will audit calls during the first month of implementation of the intervention and then randomly over the 2-year period, following adherence checklists.

Being tested
Bilingual Brain Injury Education and outpatient Navigation for Hispanic families
Keywords
Hispanic or Latino, Child, Brain Injuries, Traumatic, Patient Navigation, Rehabilitation
Medical subject headings
Brain Injuries, Traumatic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Bilingual Brain Injury Education and outpatient Navigation for Hispanic familiesBehavioural

    Also called 1stBIEN

    1st BIEN was informed by Hispanic parents and clinical providers working with them. It considers their specific needs including lack of familiarity with shared decision models and of knowledge about patient rights and eligibility for community and school services. Based on principles of Social Cognitive Theory, 1st BIEN provides TBI education, teaches problem-solving skills to promote self-efficacy and advocacy; and provides outpatient navigation that allows for observational and experiential learning while supporting access to services in a timely manner. Central to the development of our intervention is the recognition of heterogeneity in individuals' level of readiness to adopt a health behavior according to their level of self-efficacy, expectations, and environment. The 1stBIEN intervention flexibly reduces barriers to access care, and simultaneously improves parental knowledge, health literacy, and self-efficacy to optimize outcomes.

Study groups in NCT05261477
Study groupRoleWhat they receive
Intervention groupExperimentalIntervention group receives one in person education session using the 1stBIEN booklet, video education via mobile phones and care coordination from a bilingual Patient Navigator-PN for 3-months. PN follow up patients weekly for the first month and once a month for two months. Video education is done weekly. Videos cover problem solving training, brain injury concepts, rehabilitation treatments and school resources individualized to patient and family needs. PNs facilitate transition to outpatient care, follow-up with specialists and primary care providers; use of community resources; and communication with teachers and school administrators. PN provides observational and experiential learning opportunities for parents, using three way calls for scheduling of services and interactions with clinics and schools. PN calls use a problem-solving training format, to reinforce parental experiential learning and improve self-efficacy. Expert MD providers (Co-investigators) will supervise PNs.
Receives: Behavioral: Bilingual Brain Injury Education and outpatient Navigation for Hispanic families
Attention Control groupNo interventionAttention Control group receives one in person education session using the 1stBIEN booklet, monthly well-child texts and usual post-injury care including routine follow-up by specialists and primary care providers, per guidelines at each recruiting institution. Control patients have access to a list of community resources included in the 1stBIEN booklet. While education using the 1stBIEN booklet is not part of the current usual care at participating institutions, providing all families with initial education at the time of discharge addresses ethical and practical considerations. It standardizes discharge processes at participating institutions while delineating differences in the intensity of education and care coordination activities.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Receipt of follow-up care in centralized Hospital and community

    Percentage of attended appointments at hospital, primary care and therapies

    Measured: 6 months after discharge.

  2. Child's Health Related Quality of Life

    Pediatric Quality of Life Inventory-PedsQL. A 23-item questionnaire extensively used in TBI outcomes studies. It assesses physical, emotional, social and school functioning. Items on the PedsQL are reverse scored and transformed to a 0-100 scale. Higher scores indicate better health related quality of life, a clinically meaningful difference is 4.5 points. Minimum score is 0 maximum score is 100.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

Secondary outcomes (12)
  1. Child's Functional Independence

    Functional independence measures (FIM) FIM (8+ years) and WeeFIM (3-7 years);18 items (mobility 5 items, self-care 8 items and cognition 5 items) objective functional measures of independence. Every item is scored from"1" (dependent) to "7" (independent).The possible total score ranges from 18 (lowest) to 126 (highest) level of independence. For each item Scores of 1 (total assistance) and 2 (maximal assistance) belong to the "Complete Dependence" category. Scores of 3 (moderate assistance), 4 (minimal contact assistance), and 5 (supervision or set-up) belong to the "Modified Dependence" category. Scores of 6 (modified independence) and 7 (complete independence) belong to the "Independent" category.

    Measured: 24 hours before hospital discharge and through study completion an average of 6 months

  2. Child's Communication

    Adaptive Behavior Assessment System Third Edition (ABAS 3) -Communication subscale. A norm referenced measurement designed to assess adaptive skills. For both subscales, the mean and standard deviation values for healthy individuals are 10 mean and 3SD; higher scores indicate better functioning, and lower scores ,indicate below-average functioning.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  3. Child's Social Skills

    Patient-Reported Outcomes Measurement Information System (PROMIS) Parent Proxy-Peer Relationships (SF7a).Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  4. Child's Anxiety symptoms

    Patient-Reported Outcomes Measurement Information System (PROMIS) Parent Proxy-Anxiety (SF8a) symptoms. Short version of PROMIS parental report pediatric measures of anxiety (8 items). Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  5. Child's Pain Interference

    Patient-Reported Outcomes Measurement Information System PROMIS Parent Proxy-Pain Interference (SF8a). pain interference (8 items).Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  6. Child's Physical Function-Upper Extremity

    Patient-Reported Outcomes Measurement Information System PROMIS Parent Proxy-Physical Function of Upper Extremity (SF8a) .Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  7. Child's Academic Performance

    School GPA

    Measured: 1 Year before the injury and 1 year after the injury

  8. Child's Fatigue

    Patient-Reported Outcomes Measurement Information System PROMIS Parent Proxy - Fatigue (SF 10a). Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge

  9. Child's Self-care Skills

    Adaptive Behavior Assessment System Third Edition (ABAS 3) - Self-Care subscale. A norm referenced measurement designed to assess adaptive skills. The mean and standard deviation values for healthy individuals are 10 mean and 3SD; higher scores indicate better functioning, and lower scores ,indicate below-average functioning.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  10. Child's Depressive Symptoms

    Patient-Reported Outcomes Measurement Information System (PROMIS) Parent Proxy-Depressive Symptoms (SF6a). Short versions of PROMIS parental report pediatric measures of depression (6 items). Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  11. Child's Mobility

    Patient-Reported Outcomes Measurement Information System PROMIS Parent Proxy-Mobility v2.0 (SF8a).Symptoms are rated on a 5-point scale and converted to standard scores. The general population mean is 50 SD 10. Higher scores denote better outcomes.

    Measured: 1 month before injury, 24 hours before discharge from the hospital and 3,6, and 12 months after hospital discharge.

  12. Receipt of School support programs

    School records include information on provision of Individualized Education Programs (IEP), and 504 accommodation plans.

    Measured: 1 Year before the injury and 1 year after the injury

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Mar 2022
  2. Study start7 Jul 2022
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
Intervention group will receive one in-person education session, bi-weekly video reviews tailored to the child's injury and therapies; and, 3 months of bilingual outpatient navigation, using three way calls to model and coach problem solving skills, with parents as active participants. Attention control group will receive one in person-education session, monthly non-TBI (Well-child) texts and usual institutional follow up care. Participants in the control group do not receive video education or patient navigation.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05261477
Sponsor's protocol ID
STUDY00003331
Other IDs
R01HD103700-01A1
Acronym
1st-BIEN
Status last verified
Jan 2026
First submitted
24 Jan 2022
Last updated
13 Jan 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The 1st BIEN collaborative research group understands and agrees to comply with the NIH policy on Sharing Research Data. The PI and co-investigators from Seattle Children's Research Institute, University of Texas Southwestern Medical Center, Oregon Health and Science University, University of Washington and University of Utah; acknowledge their willingness to share de-identified data from this grant upon request to outside researchers. The database will be produced and will be completely de-identified in accordance with the definitions provided in the Health Insurance Portability and Accountability Act. The Data coordinating center at Seattle Children's will also prepare a data dictionary that provides a brief definition of every data element in the database so that individual investigators will be able to effectively use the data. After approval of 1stBIEN collaborative investigators, IRB and funding agency, controlled access to data will be granted following a data sharing agreement.

Publications

  • Jimenez N, Fuentes M, Virtue A, Alonso-Gonzalez L, Lopez E, Zhou C, Crawley D, Apkon S, Johnston B, Rivara F. Feasibility and Acceptability of a Telephone-Based Intervention for Hispanic Children to Promote Treatment Adherence After Traumatic Brain Injury: A Pilot Study. J Head Trauma Rehabil. 2021 Jul-Aug 01;36(4):274-281. doi: 10.1097/HTR.0000000000000658.

    PubMed 33656480
  • Lalji R, Koh L, Francis A, Khalid R, Guha C, Johnson DW, Wong G. Patient navigator programmes for children and adolescents with chronic diseases. Cochrane Database Syst Rev. 2024 Oct 9;10(10):CD014688. doi: 10.1002/14651858.CD014688.pub2.

    PubMed 39382077
  • Jimenez N, Williams CN, Keenan H, Rinaldi R, Fuentes M, Woodward D, Rivara FP, Zhou C, Ko LK, Bell K. Bilingual randomized controlled trial design, of a telephone-based intervention to promote rehabilitation adherence; A study focus on recruitment of Hispanic children with traumatic brain injury. Contemp Clin Trials. 2023 Dec;135:107362. doi: 10.1016/j.cct.2023.107362. Epub 2023 Oct 16.

    PubMed 37852531

Questions about this trial

What is this clinical trial studying?

A study testing Bilingual Brain Injury Education and outpatient Navigation for Hispanic families in people with Brain Injuries, Traumatic and Rehabilitation, run by Seattle Children's Hospital at 6 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Maria A Oliva, MS (206 884 2506, Andrea.Oliva@seattlechildrens.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Receipt of follow-up care in centralized Hospital and community (time frame: 6 months after discharge.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05261477, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jan 2026.

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