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.
Women of reproductive age.
Women with Chronic Pelvic Pain having no pathological or anatomical causes.
Women with Overactive Bladder Syndrome.
Women with Vulvodynia. -
Women experiencing perimenopause or menopause.
Women with medical, or gynecological or hormonal abnormalities.
Women with mental disorders.
Women who use substances. -
Islamia University of Bahawalpur
Lead sponsor