CBT-cp
BehavioralThe participants in CBT-cp arm will receive weekly sessions of Cognitive Behavior Therapy for Chronic Pain.
NCT Number: NCT07042555
The study will employ 4 treatment arms and 1 placebo arm to compare efficacy of CBT, PFT, Pharmacotherapy, Integrated CBT and PFT modalities in the management of chronic pelvic pain in women.
Trial opening soon.
Get Notified18 year–50 year
Female
Interventional
Not applicable
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Women of reproductive age, Women with CPP having no pathological or anatomical causes, Women with Overactive Bladder Syndrome Women with Vulvodynia.
Exclusion criteria
Women experiencing per-menopause or menopause, Women with medical, or gynecological or hormonal abnormalities, Women with mental disorders, Women who use substances.
The participants in CBT-cp arm will receive weekly sessions of Cognitive Behavior Therapy for Chronic Pain.
The participants in PFT arm will receive weekly sessions of pelvic floor therapy.
The participants in Pharmacotherapy arm will receive prescription and non prescription pain medication.
The participants in integrated arm will receive weekly sessions of both CBT-cp and PFT.
The participants in placebo arm will receive sham drug.
Time frame: Up to 12 weeks
Islamia University of Bahawalpur
Other
Efficacy of Cognitive Behavior Therapy, Pelvic Floor Therapy and Pharmacotherapy in the Treatment of Chronic Pelvic Pain in Women: A Comparative Study
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