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Efficacy of Cognitive Behavior Therapy for Treatment of Chronic Pelvic Pain in Women

Efficacy of Cognitive Behavior Therapy, Pelvic Floor Therapy and Pharmacotherapy in the Treatment of Chronic Pelvic Pain in Women: A Comparative Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07042555
Enrollment
40
Registered
2025-06-29
Start date
2025-07-10
Completion date
2025-12-30
Last updated
2025-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pelvic Pain Syndrome

Keywords

Chronic Pelvic Pain, Pelvic Pain, Women

Brief summary

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.

Interventions

BEHAVIORALCBT-cp

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.

COMBINATION_PRODUCTCBT-cp+PFT

The participants in integrated arm will receive weekly sessions of both CBT-cp and PFT.

OTHERPlacebo

The participants in placebo arm will receive sham drug.

Sponsors

Islamia University of Bahawalpur
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
The Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)Up to 12 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026