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OpenTrials
Completed

NCT Number: NCT02777294

Evaluation of Web-Based CBT for Rape Victims

Rape is unfortunately a common experience among women, affecting between 13 and 20%. In addition, up to 50% of all rape victims experience significant and persistent psychological distress. While cognitive-behavioral interventions have been found to be successful at alleviating distress among victims; the majority do not seek out these services, often because of feelings of stigma and self-blame. One potential method for circumventing these barriers is through online administered treatment. Thus, the current project is designed to conduct an initial evaluation of a 12 to 16-week, therapist-facilitated, multi-media, cognitive-behavioral, online intervention tailored specifically for rape victims. The effectiveness of this program at ameliorating distress among college women who have experienced rape and have current posttraumatic stress disorder (PTSD) was evaluated. Reductions in psychological distress was the primary outcome and was assessed at post-intervention and at three and six month follow-up periods. The effectiveness of the intervention was compared to a psycho-educational website.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Current rape-related PTSD
  • Regular access to a computer
  • English language literacy
  • Experience of completed rape at age 14 years or older

Exclusion criteria

  • No current PTSD
  • Current psychotherapy
  • Lack of stability on psychotropic medication (< 3 months)
  • Lack of literacy in English
  • Current substance dependence
  • Current elevated suicidality
  • Severe acute distress
  • No experience of completed rape after age 14

Treatment and study plan

Online intervention

Behavioral

Therapist-facilitated, multimedia, cognitive-behavioral online intervention targeting rape-related PTSD

Psycho-educational website

Behavioral

Psycho-educational self-help website about rape-related PTSD

Primary outcomes

  1. Change in PTSD symptoms (PTSD Symptom Scale Interview)

    Time frame: Change in PTSD symptoms from baseline to 3 months post intervention

Sponsors and collaborators

Lead sponsor

East Carolina University

Other

Collaborators

  • Boston University
  • University of Houston

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
May 19, 2016
Registry last updated
May 19, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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