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临床试验/NCT06445790
NCT06445790尚未招募不适用

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

Islamia University of Bahawalpur0 个研究点目标入组 60 人开始时间: 2024年6月20日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
主要终点
Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

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

排除标准

  • Women experiencing perimenopause or menopause.
  • Women with medical, or gynecological or hormonal abnormalities.
  • Women with mental disorders.
  • Women who use substances. -

结局指标

主要结局

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

时间窗: Up to 16 weeks

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

次要结局

未报告次要终点

研究者

发起方
Islamia University of Bahawalpur
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bushra Akram

PhD Scholar

Islamia University of Bahawalpur

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