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The effect of training on premenstrual syndrome among high school girls

Phase 3
Conditions
premenstrual syndrome.
Z55-Z65
XXII Codes
Registration Number
IRCT2014111519967N1
Lead Sponsor
Vice President for Research, Ilam University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
118
Inclusion Criteria

students with the age range of 15-18 years, having regular and normal menstruation periods (with intervals of 21 to 35 days and duration of 3 to 7 days). ;Exclusion criteria consisted of unwillingness to participate in the study and lack of proper registration for daily forms.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduce the symptoms of premenstrual syndrome. Timepoint: Prior to and two months following the intervention. Method of measurement: Questionnaire psst (Premenstrual Symptoms Screening Tool: PSST).
Secondary Outcome Measures
NameTimeMethod
Improved quality of life in a long term. Timepoint: Prior to and two months following the intervention. Method of measurement: Questionnare psst (Premenstrual Symptoms Screening Tool: PSST).
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