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A Randomized Clinical Trial for Women With Vulvodynia

NCT00607490 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2016-05-23

No results posted yet for this study

Summary

This study will evaluate the relative effectiveness of cognitive-behavioral therapy and supportive psychotherapy for the treatment of women with vulvodynia.

Conditions

  • Vulvodynia

Interventions

BEHAVIORAL

Cognitive-Behavioral Therapy

Behavioral, cognitive, sex therapy and relaxation interventions administered to teach self-management skills for pain control.

BEHAVIORAL

Supportive Psychotherapy

Patient-centered talk therapy to assist participants in expressing their thoughts and feelings.

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    lead NIH

Principal Investigators

  • Robin M Masheb, Ph.D. · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-09-30
Primary Completion
2005-03-31
Completion
2005-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00607490 on ClinicalTrials.gov