Acupressure therapy in premenstrual syndrome

Phase 3

Recruiting

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

• Registration Number: IRCT20190430043433N1
• Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 August 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

The desire to participate in the study
Regular menstruation from 24 to 35 days
The normalization of the length and volume of menstrual bleeding is 3-10 days
Age range 18 to 35 years
Having a Body Mass (25 -5/18)
. Having symptoms of premenstrual syndrome in two cycles before starting the intervention
Non-Depression Based on the Beck Questionnaire
Having a phone number to follow

Exclusion Criteria

Having known psychological illnesses (according to the person)
Use of any drug for the treatment of premenstrual syndrome
Tobacco use, narcotics and psychotropic drugs (according to the person)
Having regular exercise
Use of antidepressants, sedation and hormones and vitamin supplements
There are skin lesions in acupressure points
A stressful incident in the past six months, such as: separation of parents, death of first-degree family members, and ....
Use of any drug that has fluoxetine interactions

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Physical symptoms of premenstrual syndrome. Timepoint: Two months before the intervention, during the intervention, three months after the end of the intervention. Method of measurement: Daily Record of Severity of Problems chart.;Psychosomatic symptoms of premenstrual syndrome. Timepoint: Two months before the intervention, during the intervention, three months after the end of the intervention. Method of measurement: Daily Record of Severity of Problems chart.