A Mindfulness-based Intervention for Sexual Assault Survivors (NCT07515586) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
A Mindfulness-based Intervention for Sexual Assault Survivors
United States120 participantsStarted 2027-10-04
Plain-language summary
The goal is this pilot randomized trial is to learn if intervention 1 is feasible and acceptable. A secondary aim is to learn if intervention 1 reduces alcohol misuse and tobacco use in sexual assault survivors. The main questions it aims to answer are:
* Is intervention 1 feasible to implement?
* Is intervention 1 an acceptable intervention among the primary population, sexual assault survivors?
* Does intervention 1 reduce alcohol misuse and tobacco use?
Researchers will compare intervention 1 to an attention-placebo control group (e.g., online resources on healthy eating and nutrition).
Participants will:
* take online surveys at baseline, 1 month follow-up, and 3-month follow-up
* answer text-message questions at baseline and post-test
* view and engage in an educational program
Who can participate
Age range
18 Years – 24 Years
Sex
ALL
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:
* 18-24 years of age
* currently enrolled as a full-time undergraduate at GSU
* self-reported lifetime SV victimization
* self-reported SV victimization in the past 6 months
* drank alcohol within the last 30 days
* must own a smartphone
Exclusion Criteria:
* not applicable
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
Recruitment and retention of 70% of the sample at 3-month follow-up
Timeframe: 3 month follow-up
2
Acceptability of the mindfulness-based intervention benchmark of 80% self-reported acceptability