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ENGAGE-TBI Feasibility Study

ENGAGE-TBI Feasibility Study

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07549997
Enrollment
30
Registered
2026-04-24
Start date
2026-08-17
Completion date
2028-04-01
Last updated
2026-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

TBI (Traumatic Brain Injury)

Brief summary

This study will first evaluate the feasibility of delivering the ENGAGE-TBI intervention in a community setting with adults with TBI.

Detailed description

Social isolation is a prevalent and highly prioritized concern among people with traumatic brain injury (TBI), contributing to poor physical and mental health outcomes. Existing rehabilitation interventions have focused primarily on remediating underlying impairments, with limited success in improving social participation. A patient-directed, self-management approach may offer a promising alternative. This study aims to evaluate the feasibility of ENGAGE-TBI, a novel, theory-driven occupational therapy intervention designed to reduce social isolation by increasing social participation among community-dwelling adults with TBI. Using a single-group pre-post design, this study will enroll 30 adults with TBI recruited through the Brain Injury Association of Missouri. ENGAGE-TBI is a 12-session group intervention co-facilitated by an occupational therapist and a peer mentor with TBI. The intervention integrates three core elements - social learning, guided problem-solving, and skilled community practice - delivered across six weeks. Feasibility outcomes include fidelity, participant engagement, satisfaction, attendance, and retention. The primary clinical outcome is social participation, measured using the PROMIS Ability to Participate in Social Roles and Activities. Feasibility outcomes will be examined descriptively against pre-specified benchmarks. Within-group Cohen's d effect sizes with 95% confidence intervals will be calculated to estimate intervention effects and variability, informing the design of a future randomized controlled trial. Findings will support the development of a fully-powered effectiveness trial. This study addresses a critical gap in TBI rehabilitation by testing a stakeholder-informed, community-based intervention that treats TBI as a chronic condition and prioritizes patient-directed goal achievement over impairment remediation.

Interventions

BEHAVIORALSocial intervention study for TBI survivors

ENGAGE-TBI is a community-based group intervention that is co-facilitated by an occupational therapist and a person with a brain injury. ENGAGE-TBI incorporates social learning, guided problem-solving, and skilled practice of strategies to achieve social participation goals. It is delivered in 12 90-minute group sessions that are held twice per week for 6 weeks. Aside from community outings, sessions will take place at the Brain Injury Association of Missouri on a separate day and time from education group sessions.

Sponsors

Washington University School of Medicine
Lead SponsorOTHER
American Occupational Therapy Foundation
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* at least 18 years old * experienced a TBI \> 6 months prior to enrollment, confirmed by a physician as documented in their medical record * live in the St. Louis area * report problems with social participation (retention of \< 80% of pre-TBI social activities as measured by Activity Card Sort)

Exclusion criteria

* insufficient English language fluency to participate in the group intervention * have active substance use disorder (PRIME-MD MINI) * have an untreated psychotic disorder (PRIME-MD MINI) * have severe memory impairment that would limit their ability to recall strategies with support (Montreal Cognitive Assessment, \< 21)

Design outcomes

Primary

MeasureTime frameDescription
Client Satisfaction Questionnaire-8Post-Treatment (6-weeks)8-item measure of intervention satisfaction with a 4-point Likert scale (8-32); higher scores indicate greater satisfaction
Pittsburgh Rehabilitation Participation ScaleImmediately at the conclusion of each intervention session (included as part of the interventionist's session documentation)Interventionist-administered measure of engagement in each intervention session; reported on a 1-6 scale, with higher scores indicating greater participation.
PROMIS (Patient-Reported Outcome Measures Information System) Ability to Participate in Social Roles and ActivitiesBaseline, Post-Treatment (6-weeks)Computer adaptive test examining social participation abilities; scores reported as T-scores (0-100 scale, with higher scores indicating greater participation)

Secondary

MeasureTime frameDescription
PROMIS (Patient-Reported Outcome Measures Information System) Social IsolationBaseline, Post-Treatment (6-weeks)Computer Adaptive Test examining social isolation; scores reported as T-scores (0-100 scale, higher scores indicate higher isolation)
PROMIS-29 (Patient-Reported Outcome Measures Information System)Baseline, Post-Treatment (6-weeks)29-item measure of multiple health domains using a 5-point Likert scale and reported as T-scores (0-100 scale, lower scores indicate greater health)

Countries

United States

Contacts

CONTACTJessica Kersey, PhD, OTR/L Assistant Professor, PhD, OTR/L
jkersey@wustl.edu+1 314 273 7540
CONTACTCurtis Comer, Clinical Research Coordinator I, High School
curtisccomer@wustl.edu+1 314 273 3288

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026