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 range18 Years – 75 Years

SexALL

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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)

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