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临床试验/NCT07042555
NCT07042555尚未招募不适用

Efficacy of Cognitive Behavior Therapy, Pelvic Floor Therapy and Pharmacotherapy in the Treatment of Chronic Pelvic Pain in Women: A Comparative Study

Islamia University of Bahawalpur0 个研究点目标入组 40 人开始时间: 2025年7月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
主要终点
The Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ)

研究概览

简要总结

The study will employ 4 treatment arms and 1 placebo arm to compare efficacy of CBT, PFT, Pharmacotherapy, Integrated CBT and PFT modalities in the management of chronic pelvic pain in women.

研究设计

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

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Women of reproductive age, Women with CPP having no pathological or anatomical causes, Women with Overactive Bladder Syndrome Women with Vulvodynia.

排除标准

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

研究组 & 干预措施

Integrated CBT-cp and PFT

Experimental

干预措施: CBT-cp+PFT (Combination Product)

Cognitive Behavior Therapy for Chronic Pain (CBT-cp)

Experimental

干预措施: CBT-cp (Behavioral)

Pharmacotherapy

Experimental

干预措施: Pharmacotherapy (Drug)

Pelvic Floor Therapy (PFT)

Experimental

干预措施: Pelvic Floor Therapy (Other)

Placebo

Placebo Comparator

干预措施: Placebo (Other)

结局指标

主要结局

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

时间窗: Up to 12 weeks

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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