---
title: Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women
nct_id: NCT06445790
overall_status: NOT_YET_RECRUITING
phase: NA
sponsor: Islamia University of Bahawalpur
study_type: INTERVENTIONAL
primary_condition: Chronic Pelvic Pain Syndrome
canonical_url: "https://parkinsonspathways.com/agent/trials/NCT06445790.md"
clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT06445790"
ct_last_update_post_date: 2024-06-06
last_seen_at: "2026-05-12T06:05:43.113Z"
source: ClinicalTrials.gov (mirrored, no enrichment)
---
# Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women

**Official Title:** Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women: A Randomized Controlled Trial

**NCT ID:** [NCT06445790](https://clinicaltrials.gov/study/NCT06445790)

## Key Facts

- **Status:** NOT_YET_RECRUITING
- **Phase:** NA
- **Study Type:** INTERVENTIONAL
- **Target Enrollment:** 60
- **Lead Sponsor:** Islamia University of Bahawalpur
- **Conditions:** Chronic Pelvic Pain Syndrome
- **Start Date:** 2024-06-20
- **Completion Date:** 2024-10-20
- **CT.gov Last Update:** 2024-06-06

## Brief Summary

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

- **Minimum age:** 18 Years
- **Maximum age:** 45 Years
- **Sex:** FEMALE
- **Healthy Volunteers:** No

```
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. -
```

## Arms

- **Group A** (EXPERIMENTAL) — It will receive 12 sessions of Cognitive Behavior Therapy for Chronic Pelvic Pain.
- **Group B** (NO_INTERVENTION) — Group B will be control group.

## Interventions

- **Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp** (BEHAVIORAL) — CBT-cp will be administered weekly sessions for 12 weeks.

## Primary Outcomes

- **Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)** _(time frame: Up to 16 weeks)_ — Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)

## Recent Field Changes (last 30 days)

- `status.overallStatus` — added _(2026-05-12)_
- `status.primaryCompletionDate` — added _(2026-05-12)_
- `status.completionDate` — added _(2026-05-12)_
- `status.lastUpdatePostDate` — added _(2026-05-12)_
- `design.phases` — added _(2026-05-12)_
- `design.enrollmentCount` — added _(2026-05-12)_
- `eligibility.criteria` — added _(2026-05-12)_
- `eligibility.minAge` — added _(2026-05-12)_
- `eligibility.maxAge` — added _(2026-05-12)_
- `eligibility.sex` — added _(2026-05-12)_
- `outcomes.primary` — added _(2026-05-12)_
- `armsInterventions.arms` — added _(2026-05-12)_
- `armsInterventions.interventions` — added _(2026-05-12)_
- `sponsor.lead` — added _(2026-05-12)_
- `results.hasResults` — added _(2026-05-12)_

---

*Canonical: https://parkinsonspathways.com/agent/trials/NCT06445790.md*  
*Source data (authoritative): https://clinicaltrials.gov/study/NCT06445790*  
*This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*