The effect of resiliency on premenstrual syndrome

Not Applicable

Completed

• Conditions: premenstural syndrome.; Premenstrual tension syndrome

• Registration Number: IRCT2015052615341N6
• Lead Sponsor: Vice Chancellor of Research the Technology, Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

15-17 year-old high school girls; Resident of Hamedan; Having moderate to severe premenstrual syndrome scores (scores of 19 and up); The lack of effective drug treatment for the syndrome such as Sedatives, hypnotics, hormones and anti prostaglandins; The lack of a history of physical and mental diseases; Passing at least 6 menstrual cycles and exclusion criteria: Effective drug treatment on the syndrome such as Sedatives, hypnotics, hormones and anti prostaglandins; The occurrence of events such as the death or illness of relatives; Failure to attend two consecutive meetings

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Premenstrual syndrome. Timepoint: Before and after the intervention. Method of measurement: Standard questionnaire PSST(Premenstrual Symptoms Screening Tool).

Secondary Outcome Measures

Name	Time	Method
Resiliency. Timepoint: Before and after intervention. Method of measurement: Connor-Davidson Resilience questionnaire.