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临床试验/IRCT20201027049164N2
IRCT20201027049164N2招募中未知

Comparative investigation between the effectiveness of Achillea wilhelmsii tablet and group counseling based on acceptance and commitment on Pre Menstrual Syndrome (PMS) symptoms in students living in the dormitories

Kerman University of Medical Sciences0 个研究点目标入组 264 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
264

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 45 years(—)
性别
Female

入选标准

  • All samples should have a menstrual cycle duration of 35-24 days.
  • Being single
  • The age of the samples should be between 18-45 years.
  • Samples with premenstrual syndrome for at least six months and tend to participate in the study.
  • Do not have any mental or physical illness.
  • Do not take any chemical and herbal medicines
  • Do not take birth control pills
  • Have at least one symptom of mental and physical symptoms that should begin 16 days after menstruation

排除标准

  • Menstrual period is less than 3 days and more than 8 days
  • Interval of menstrual cycles less than 24 days and more than 35 days
  • Existence of severe stress in the last trimester such as: death of relatives, marriage or surgery
  • Pregnant and lactating women
  • Participating in a simultaneous counseling program

研究者

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