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临床试验/NCT04235595
NCT04235595已完成不适用

Comparison of the Effects of High-frequency TENS and Connective Tissue Manipulation on the Primary Dysmenorrhea

Izmir Bakircay University0 个研究点目标入组 40 人开始时间: 2015年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
主要终点
Assessment of Pain Severity

研究概览

简要总结

this study was to compare the early and short-term effects of high-frequency transcutaneous electrical nerve stimulation (TENS) versus connective tissue manipulation (CTM) in participants with primary dysmenorrhea. Half of the participants received CTM, while the other half received TENS.

详细描述

CTM and TENS each relieve dysmenorrhea pain, but they do so by different. The electrotherapy modality that is most commonly used in the treatment of dysmenorrhea is TENS. It has been reported in studies that high-frequency TENS is more effective in reducing pain than either low-frequency TENS or placebo TENS.

A scan of the literature reveals that although there are differing opinions and applications related to the number and duration of CTM, it has been shown that women with primary dysmenorrhea experience reduced pain after CTM,

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
None

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • being between the ages of 18-30
  • having a diagnosis of primary dysmenorrhea

排除标准

  • having used an oral contraceptive in the last 3 months,
  • having an active sexual life,
  • pregnancy,
  • having gone through childbirth,
  • having a neurological deficit,
  • any kind of systemic condition,
  • a diagnosed gynecological condition (pelvic inflammatory diseases, endometriosis, uterus cancers, ovarian cysts, etc.),
  • taking psychotherapeutic drugs.

结局指标

主要结局

Assessment of Pain Severity

时间窗: Change from Pain severity at 3 months

To determine the localization of pain, the participants were asked to point out and mark the place(s) they felt the most pain on a body diagram. The severity of the pain of dysmenorrhea was assessed on a 10-cm Visual Analog Scale (VAS).

次要结局

  • Assessment of Depressive Symptoms(Change from Beck Depression Inventory score at 3 months)
  • Assessment of Anxiety(Change from Beck Anxiety Inventory score at 3 months)
  • Assessment of Sleep Disorders and Fatigue(Change from Sleep Disorders and Fatigue severity at 3 months)
  • Assessment of General Health Status(Change from General Health Questionnaire score at 3 months)

研究者

发起方
Izmir Bakircay University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Nilay Yürekdeler Şahin

Assistant Professor

Izmir Bakircay University

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