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

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

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-20

Study Completion Date

2024-10-20

Brief Summary

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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.

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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

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Group A

It will receive 12 sessions of Cognitive Behavior Therapy for Chronic Pelvic Pain.

Group Type EXPERIMENTAL

Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp

Intervention Type BEHAVIORAL

CBT-cp will be administered weekly sessions for 12 weeks.

Group B

Group B will be control group.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp

CBT-cp will be administered weekly sessions for 12 weeks.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Women of reproductive age.
2. Women with Chronic Pelvic Pain having no pathological or anatomical causes.
3. Women with Overactive Bladder Syndrome.
4. Women with Vulvodynia. -

Exclusion Criteria

1. Women experiencing perimenopause or menopause.
2. Women with medical, or gynecological or hormonal abnormalities.
3. Women with mental disorders.
4. Women who use substances. -

Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No