Cognitive behavioral therapy for women's sexual dysfunction
THE INFLUENCE OF COGNITIVE BEHAVIORAL THERAPY IN SEXUAL DYSFUNCTION FEMALE: Randomized Clinical Trial
This study is testing if cognitive-behavioral therapy can help improve sexual function and quality of life for women aged 18-59 who are experiencing sexual dysfunction.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 34 (estimated) |
| Ages | 18 Years to 59 Years |
| Sex | Female |
| Sponsor | Centro de Atenção ao Assoalho Pélvico Academic / other |
| Locations | 1 site (Salvador, Estado de Bahia) |
| Trial ID | NCT02613546 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the impact of cognitive-behavioral therapy (CBT) on the quality of life and sexual function in women experiencing sexual dysfunction. It aims to address a gap in existing research by assessing how CBT techniques can improve sexual health and overall well-being. Participants will be randomized to receive either CBT or a control therapy, with outcomes measured through established scales. The study focuses on women aged 18-59 with specific criteria related to sexual function.
Who should consider this trial
Good fit: Ideal candidates are women aged 18-59 with a Female Sexual Function Index (FSFI) score of 26 or lower.
Not a fit: Patients with moderate to severe depression as indicated by Beck Scales or those receiving hormone therapy may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide an effective non-pharmacological treatment option for women suffering from sexual dysfunction.
How similar studies have performed: While CBT has shown efficacy in various mental health disorders, this specific application for sexual dysfunction is novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women aged 18-59 years; * FSFI less than or equal to 26. Exclusion Criteria: * Scores of Beck Scales - moderate or severe; * Prescribing hormone therapy after starting the group.
Where this trial is running
Salvador, Estado de Bahia
- Centro de Atenção ao Assoalho Pelvico — Salvador, Estado de Bahia, Brazil (Recruiting)
Study contacts
- Principal investigator: Patricia V Lordelo, PhD — Centro de Atenção ao Assoalho Pélvico - BAHIANA
- Study coordinator: Patricia V Lordelo, Phd
- Email: pvslordelo@hotmail.com
- Phone: +5571988592400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.