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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorIslamia University of Bahawalpur

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Women of reproductive age.

Women with Chronic Pelvic Pain having no pathological or anatomical causes.

Women with Overactive Bladder Syndrome.

Women with Vulvodynia. -

Disqualifiers

Women experiencing perimenopause or menopause.

Women with medical, or gynecological or hormonal abnormalities.

Women with mental disorders.

Women who use substances. -

Trial design

Design model

Parallel

Treatments tested in this trial

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

    Behavioral

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

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Group AExperimental treatment 1 intervention
Group B: Group BNo intervention 0 interventions

Trial outcomes

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

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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