Trauma-informed Intervention to Reduce Substance Use and to Support Community Transition (NCT06651528) | Clinical Trial Compass
By InvitationNot Applicable
Trauma-informed Intervention to Reduce Substance Use and to Support Community Transition
United States264 participantsStarted 2025-12-09
Plain-language summary
The overall aim of this study is to reduce overdose risk for criminal legal system (CLS) involved women during community re-entry through the adaptation and testing of an innovative, trauma-informed, relational intervention approach (Trust-Based Relational Intervention or TBRI).
Who can participate
Age range
18 Years – 99 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* participating in corrections-based SUD treatment
* have an anticipated parole eligibility date within 4 months
* self-identified history of violent victimization
* are willing to work with at least one person living in the community who will be supportive of your recovery when you get out
* interested in participating in the study
Exclusion Criteria:
* not participating in corrections-based SUD treatment
* anticipated parole eligibility date greater than 4 months
* no self-identified history of violent victimization
* not willing to work with at least one person living in the community who will be supportive of your recovery when you get out
* not interested in participating in the study
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in overdose risk
Timeframe: Baseline and at 3 and 6 months post-release from prison