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

Not Applicable

Not yet recruiting

• Conditions: Chronic Pelvic Pain Syndrome
• Interventions: Behavioral: Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp

• Registration Number: NCT06445790
• Lead Sponsor: Islamia University of Bahawalpur

Brief 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-03-29
• Status Verified: 2024-06
• Study First Submitted QC: 2024-06-05
• Last Update Submitted: 2024-06-05
• Study First Posted: 2024-06-06
• Last Update Posted: 2024-06-06
• Study Start: 2024-06-20
• Primary Completion: 2024-10-20
• Study Completion: 2024-10-20

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 60

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

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group A	Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp	It will receive 12 sessions of Cognitive Behavior Therapy for Chronic Pelvic Pain.

Primary Outcome Measures

Name	Time	Method
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)	Up to 16 weeks	Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)