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Implementation of TBI-RECOVER in Substance Use Treatment

The Ohio State University logo

The Ohio State University

Status

Not yet enrolling

Conditions

Traumatic Brain Injury
Substance Use Disorder (SUD)

Treatments

Behavioral: Control
Behavioral: TBI-RECOVER

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07215221
1K01DA060881-01A1 (U.S. NIH Grant/Contract)
20251658

Details and patient eligibility

About

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.

Enrollment

900 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patient Inclusion Criteria:

  • English-speaking; diagnosed with a substance use disorder; assigned to an outpatient provider for psychotherapy at the treatment clinic participating in the study.

Patient Exclusion Criteria:

  • None

Provider Inclusion Criteria:

- All providers employed in the outpatient treatment clinic who deliver psychotherapy are eligible (e.g., social workers, counselors, psychologists).

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

900 participants in 2 patient groups

TBI-RECOVER treatment arm
Experimental group
Description:
Patients the treatment arm will be screened for brain injury, and those with a positive screen will receive the full TBI-RECOVER intervention model.
Treatment:
Behavioral: TBI-RECOVER
Control arm
Active Comparator group
Description:
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.
Treatment:
Behavioral: Control

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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