CompletedNot Applicable

RRT for PTSD Symptoms in Survivors of Sexual Violence

United States30 participantsStarted 2020-11-15

Plain-language summary

Study to provide evidence of efficacy for Rapid Resolution Therapy in symptoms of PTSD, Anxiety, and Depression in survivors of sexual violence.

Who can participate

Age range

18 Years – 75 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: * 18-70 years old * self report experiencing a rape any time before 3 months prior to treatment * on PCL-C (Positive for PTSD) * score 3-5 on at least one item 1-5 * score 3-5 on at least 3 items 6-12 * score 3-5 on at least 2 items 13-17 Exclusion Criteria: * history of schizophrenia or psychosis current * suicidal risk * in an ongoing threatening situation (i.e. domestic violence) * participants who are pregnant or become pregnant during the study (if someone becomes pregnant during the study, we will complete treatment if she desires, but will not include data)

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

Change in The Clinician-Administered PTSD Scale (CAPS-5: Weathers et al, 2015)

Timeframe: pre-intervention (one month version), one week post intervention (past week version) , 6 months post intervention (one month version)

Change in PTSD Symptom Scale Self-Report- Civilian Version (PSS-SR: Foa et al, 1993)

Timeframe: screening, one week post-treatment, 6 month follow up

Change in Beck Depression Inventory (BDI): beck et al, 1988)

Timeframe: pre-intervention, one week post intervention, 6 month follow up

Change in The State Trait Anxiety Inventory (STAI: Spielberger et al, 1970)

Timeframe: Pre-intervention, one week follow up, 6 month follow up

Trial details

NCT IDNCT04073004

SponsorUniversity of Colorado, Denver

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-06-30

View on ClinicalTrials.gov More PTSD trials