About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Women of reproductive age.
Women with Chronic Pelvic Pain having no pathological or anatomical causes.
Women with Overactive Bladder Syndrome.
Women with Vulvodynia. -
Disqualifiers
Women experiencing perimenopause or menopause.
Women with medical, or gynecological or hormonal abnormalities.
Women with mental disorders.
Women who use substances. -
Trial design
Parallel
Treatments tested in this trial
Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp
BehavioralCBT-cp will be administered weekly sessions for 12 weeks.
Treatment groups
Trial outcomes
Primary outcomes
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: