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

Not Applicable

Recruiting

• Conditions: Premenstrual Syndrome.; Premenstrual tension syndrome; N94.3

• Registration Number: IRCT20201027049164N2
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 264

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Symptoms of premenstrual syndrome. Timepoint: Beginning of the study (before the start of the intervention) and end of the intervention. Method of measurement: Daily Symptom Report Questionnaire (DSR).