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Clinical Trials/IRCT20201027049164N2
IRCT20201027049164N2
Recruiting
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 sites264 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Premenstrual Syndrome.
Sponsor
Kerman University of Medical Sciences
Enrollment
264
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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