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临床试验/NCT05395156
NCT05395156Unknown不适用

EFFECT OF TENS ON ACUPOINTS IN PREMENSTRUAL SYNDROME

Cairo University0 个研究点目标入组 50 人开始时间: 2022年6月10日最近更新:
适应症

试验速览

阶段
不适用
入组人数
50
主要终点
pain severity

研究概览

简要总结

These will be no effect of transcutaneous electrical acupoint stimulation on premenstrual syndrome Does transcutaneous electrical acupoint stimulation affect premenstrual syndrome (PMS)?

详细描述

Premenstrual syndrome is a collection of emotional, physiological, and behavioral symptoms that develop around the end of the luteal phase and fade away with or after menstruation Due to limited evidence on the efficacy of sustained progesterone and the side effects of antidepressant and anxiolytics, in some cases, alternative therapies are recommended for patients with PMS TEAS may be more effective than other forms of transcutaneous electrical nerve stimulation (TENS) in modulating brain activity because acupoint areas contain relatively denser neural and neuroactive components than non-acupoint areas TEAS has been reported to have similar efficacy as acupuncture, electrical acupuncture, and TENS

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 (Investigator)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Their age will range from 18 to 25 years.
  • The regularity of menstrual cycle is 28-35 days.
  • All of them suffering from moderate and sever PMS.
  • All participants are virgin.
  • Their BMI will range from 25-30 kg\m2.

排除标准

  • Any pathological findings in the pelvic cavity as PCO, Endometriosis and pelvic inflammatory disease.
  • Any history of gynecological intervention.
  • Have any condition impedes the use of electrotherapy.
  • Receiving sedatives or any medical treatment.
  • Having irregular menstruation.

结局指标

主要结局

pain severity

时间窗: Up to 3 monthes

The pain intensity will be assessed through visual analogue scale (VAS) for each participant in both groups before and after treatment Each participant will be asked to mark a point on VAS line between the extremes that related to her current pain intensity

premenstrual syndrome severity

时间窗: up to 3 monthes

Participants can differentiate between their experiences of different symptoms during menstrual cycle and they will be assessed before and after treatment using the Menstrual Distress Questionnaire (MDQ) Each participant will be asked to rate their experience of each of the symptoms on the MDQ on a scale ranging from no experience of the symptom to an acute or partially disabling experience of the symptom

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aml Mohammed Elsayed Abdelaal

spicialist of physical therapy at talkha central hospital

Cairo University

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