Status:
COMPLETED
A Randomized Clinical Trial for Women With Vulvodynia
Lead Sponsor:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Conditions:
Vulvodynia
Eligibility:
FEMALE
21-60 years
Phase:
NA
Brief Summary
This study will evaluate the relative effectiveness of cognitive-behavioral therapy and supportive psychotherapy for the treatment of women with vulvodynia.
Detailed Description
Many treatments used for women with vulvodynia are based solely upon expert opinion. This randomized trial aimed to test the relative efficacy of cognitive-behavioral therapy (CBT) and supportive psyc...
Eligibility Criteria
Inclusion
- Independently diagnosed with vulvodynia by two study physicians
Exclusion
- Any conditions known to better account for the vulvar pain
- Psychotic illness
- Actively suicidal
- Substance dependent
- Life-threatening illness
- Initiated psychotherapy, psychopharmacologic treatment or pain medication within one month prior to beginning the assessment phase of the study.
Key Trial Info
Start Date :
September 1 2000
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2005
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00607490
Start Date
September 1 2000
End Date
March 1 2005
Last Update
May 23 2016
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