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NCT06445790 Clinical Trial

Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women

Chronic Pelvic Pain Syndrome Clinical Trial

Official title:
Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women: A Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06445790
Other study ID # IUB
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 20, 2024
Est. completion date October 20, 2024

Study information
Verified date June 2024
Source Islamia University of Bahawalpur
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This will be the pilot study trial. The target population will be 30 individuals with Chronic Pelvic Pain (CCP). There will be 02 groups, Experimental Group and Control Group. The primary outcome measure will be Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ). The experimental group will receive CBT spread over 12 sessions.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 60
Est. completion date October 20, 2024
Est. primary completion date October 20, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: 1. Women of reproductive age. 2. Women with Chronic Pelvic Pain having no pathological or anatomical causes. 3. Women with Overactive Bladder Syndrome. 4. Women with Vulvodynia. - Exclusion Criteria: 1. Women experiencing perimenopause or menopause. 2. Women with medical, or gynecological or hormonal abnormalities. 3. Women with mental disorders. 4. Women who use substances. -

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp
CBT-cp will be administered weekly sessions for 12 weeks.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Islamia University of Bahawalpur

Outcome
Type Measure Description Time frame Safety issue
Primary Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ) Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ) Up to 16 weeks
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