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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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06445790
Study type Interventional
Source Islamia University of Bahawalpur
Contact
Status Not yet recruiting
Phase N/A
Start date June 20, 2024
Completion date October 20, 2024

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