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

NCT ID: NCT07042555

Last Updated: 2025-06-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-10

Study Completion Date

2025-12-30

Brief Summary

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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.

Detailed Description

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Conditions

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Chronic Pelvic Pain Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Cognitive Behavior Therapy for Chronic Pain (CBT-cp)

Group Type EXPERIMENTAL

CBT-cp

Intervention Type BEHAVIORAL

The participants in CBT-cp arm will receive weekly sessions of Cognitive Behavior Therapy for Chronic Pain.

Pelvic Floor Therapy (PFT)

Group Type EXPERIMENTAL

Pelvic Floor Therapy

Intervention Type OTHER

The participants in PFT arm will receive weekly sessions of pelvic floor therapy.

Pharmacotherapy

Group Type EXPERIMENTAL

Pharmacotherapy

Intervention Type DRUG

The participants in Pharmacotherapy arm will receive prescription and non prescription pain medication.

Integrated CBT-cp and PFT

Group Type EXPERIMENTAL

CBT-cp+PFT

Intervention Type COMBINATION_PRODUCT

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

Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type OTHER

The participants in placebo arm will receive sham drug.

Interventions

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CBT-cp

The participants in CBT-cp arm will receive weekly sessions of Cognitive Behavior Therapy for Chronic Pain.

Intervention Type BEHAVIORAL

Pelvic Floor Therapy

The participants in PFT arm will receive weekly sessions of pelvic floor therapy.

Intervention Type OTHER

Pharmacotherapy

The participants in Pharmacotherapy arm will receive prescription and non prescription pain medication.

Intervention Type DRUG

CBT-cp+PFT

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

Intervention Type COMBINATION_PRODUCT

Placebo

The participants in placebo arm will receive sham drug.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Islamia University of Bahawalpur

OTHER

Sponsor Role lead

Responsible Party

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Bushra Akram

PhD Scholar

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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IslUB

Identifier Type: -

Identifier Source: org_study_id

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