Implementation of TBI-RECOVER in Substance Use Treatment

Part of paid clinical trials in Columbus, Ohio.

Sponsor
Ohio State University
Study ID
NCT07215221
Status
Recruiting
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Conditions

  • Substance Use Disorder (SUD)
  • Traumatic Brain Injury

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • TBI-RECOVER — BEHAVIORAL
    The TBI-RECOVER intervention model consists of three components: 1) a web-based brain injury and cognitive impairment screener using the Online Brain Injury Screening and Support System (OBISSS) of the National Association of State Head Injury Administrators, 2) brief education and information on traumatic brain injury and substance use disorders, and 3) neurocognitive accommodations, or compensatory strategies, for neurological impairment.
  • Control — BEHAVIORAL
    The control condition includes a brief information and educational sheet on traumatic brain injury and substance use disorder, how these two conditions are connected with each other, and a list of suggested accommodations they can use in treatment.

Study Details

The goal of this hybrid type 2 pilot trial is to understand the implementation and effectiveness of the TBI-RECOVER intervention model (e.g., brain injury screening, cognitive and behavioral challenges screening, and neurocognitive accommodations) on patient retention in outpatient substance use disorder treatment. We will evaluate whether an implementation strategy bundle (e.g., training/education, champions, audit \& feedback, facilitation) improves provider use and sustainability of the TBI-RECOVER intervention, and also whether the TBI-RECOVER intervention improves patient symptoms and treatment retention.

Key Dates

Start date
Apr 28, 2026
Status verified
Jul 2026
Primary completion
Jan 30, 2030
Completion
Mar 30, 2030

Study Design

Enrollment
900 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: TBI-RECOVER treatment arm
    Patients the treatment arm will be screened for brain injury, and those with a positive screen will receive the full TBI-RECOVER intervention model.
  • Active Comparator: Control arm
    Patients in the control arm will be screened for brain injury, and those with a positive screen will receive a brief information and educational sheet.

Primary Outcome Measure

Treatment retention [ Time Frame: 1 year ]

Locations (1)

FacilityCityStateZIPSite coordinators
OSU Hospital SystemColumbusOhio43210
Kathryn Hyzak, PhD
[email protected]
3802836683

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By research site
OSU Hospital System· Columbus, OH

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