CClinicalTrials.gg
Sign In
Not yet recruitingNCT06445790Updated Jun 6, 2024

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

An interventional study of Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp in Chronic Pelvic Pain Syndrome, sponsored by Islamia University of Bahawalpur. Not yet recruiting. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2024-06-06.

Sponsored by Islamia University of Bahawalpur · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Oct 2024, 1 year 11 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study 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.

02

Conditions studied

  • Chronic Pelvic Pain Syndrome

Browse trials for

Keywords

  • Chronic Pelvic Pain, Pelvic Pain, Women
03

In context

Pelvic Pain

375 studies on the registry are indexed under Pelvic Pain; 83 are open to participants now.

This study's planned enrollment of 60 is above the median of 54 across 273 interventional studies indexed under Pelvic Pain.

Browse Pelvic Pain studies →

Lead sponsor

Islamia University of Bahawalpur is the lead sponsor of 15 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts 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

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. -
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Group A

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

    Behavioral: Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp

  • No intervention
    Group B

    Group B will be control group.

Interventions

  • BehavioralCognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp

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

06

What researchers measure

Primary outcomes

  1. Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)

    Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)

    Time frame: Up to 16 weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 6, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06445790
Lead sponsor
Islamia University of Bahawalpur
Responsible party
Bushra Akram (PhD Scholar, Islamia University of Bahawalpur) — Principal investigator
First posted
Jun 6, 2024
Start date
Jun 20, 2024 (estimated)
Primary completion
Oct 20, 2024 (estimated)
Completion
Oct 20, 2024 (estimated)
Last update
Jun 6, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Other studies in this condition

Pelvic Pain→

Other studies from this sponsor

Islamia University of Bahawalpur

Start the discussion