Vulvodynia
Conditions
Keywords
Vulvodynia, Vulvar pain, Dyspareunia, Sexual dysfunction, Vestibulitis
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 psychotherapy (SPT) in women with vulvodynia. Of the 50 participants, 42 (84%) completed 10-week treatments and 47 (94%) completed one-year follow-up. Mixed effects modeling was used to make use of all available data. Participants had statistically significant decreases in pain severity (p's\<.001) with 42% of the overall sample achieving clinical improvement. CBT, relative to SPT, resulted in significantly greater improvement in pain severity during physician examination (p=.014), and greater improvement in sexual function (p=.034), from pre- to post-treatment. Treatment effects were well maintained at one-year follow-up in both groups. Participants in the CBT condition reported significantly greater treatment improvement, satisfaction and credibility than participants in the SPT condition (p's\<.05). Findings from the present study suggest that psychosocial treatments for vulvodynia are effective. CBT, a directed treatment approach that involves learning and practice of specific pain-relevant coping and self-management skills, yielded better outcomes and greater patient satisfaction than a less directive approach.
Interventions
Behavioral, cognitive, sex therapy and relaxation interventions administered to teach self-management skills for pain control.
Patient-centered talk therapy to assist participants in expressing their thoughts and feelings.
Sponsors
Study design
Eligibility
Inclusion criteria
* Independently diagnosed with vulvodynia by two study physicians
Exclusion criteria
* 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Severity | Measured at 1-year follow-up |
Secondary
| Measure | Time frame |
|---|---|
| Sexual Functioning | Measured at 1-year follow-up |
| Emotional Functioning | Measured at 1-year follow-up |