RRT for PTSD Symptoms in Survivors of Sexual Violence

PTSD Clinical Trial

Official title: Rapid Resolution Therapy (RRT) for Post-traumatic Stress Disorder (PTSD) Symptoms in Survivors of Sexual Violence

Status Recruiting

Clinical Trial Summary

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

Clinical Trial Description

The investigators will recruit 24 participants to complete pre-test measures, participate in a 3 hour therapy session of Rapid Resolution Therapy (RRT), and then re-test one week post treatment and 6 months follow up.

If participants do not report a "good result" following the 3 hour session, the investigators will offer a 1.5 hour follow up session Participants will receive free therapy for their participation, but will not be paid.

Participants will be men and women over the age of 18 who do not have a diagnosis of psychosis and are not actively suicidal and have experienced a single rape at least 3 months before enrolling in the study.

Sessions will be audio recorded and transcribed for construct validity (of RRT). Identifying in formation will be removed by the study coordinator before transcripts are coded for validity.

This study proposes to use the same methods as Rothbaum et al (2005) published in Journal of Traumatic Stress that compares Prolonged Exposure to Eye Movement and Desensitization and Reprocessing (EMDR) for PTSD Rape Victims. The investigators will compare our results to theirs. Both of their treatments were 8 sessions, and this study's treatment is one. They also include data for a control group. ;

Related Conditions & MeSH terms

• PTSD
• Rape Sexual Assault
• Stress Disorders, Post-Traumatic

• NCT number: NCT04073004
• Study type: Interventional
• Source: University of Colorado, Denver
• Contact: Susan Hughes, RN
• Phone: 7197611466
• Email: susanhughes.rrt@gmail.com
• Status: Recruiting
• Phase: N/A
• Start date: November 15, 2020
• Completion date: December 2022