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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
CBT-cp will be administered weekly sessions for 12 weeks.
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)
Time frame: Up to 16 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.