Skip to content

Evaluation of Web-Based CBT for Rape Victims

Evaluation of Web-Based CBT for Rape Victims

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02777294
Enrollment
87
Registered
2016-05-19
Start date
2012-05-31
Completion date
2014-08-31
Last updated
2016-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PTSD

Brief summary

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.

Interventions

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

BEHAVIORALPsycho-educational website

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

Sponsors

Boston University
CollaboratorOTHER
University of Houston
CollaboratorOTHER
East Carolina University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Change in PTSD symptoms (PTSD Symptom Scale Interview)Change in PTSD symptoms from baseline to 3 months post intervention

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026