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The effect of distraction techniques on premenstrual syndrome

Not Applicable
Recruiting
Conditions
Premenstrual syndrome.
Premenstrual tension syndrome
N94.3
Registration Number
IRCT20151211025477N5
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
42
Inclusion Criteria

Women and girls in the age range of 14-35
At least six months have passed since their menarche
not taking medicine for reduce PMS symptoms
not participating in the same classes
have minimum reading and writing literacy
Absence of pregnancy
obtaining score 17-33 using the PMS tool
Absence to physical and mental illness as known
Absence sensitivity to Gelophen

Exclusion Criteria

Unwillingness to continue study participation
Pregnancy during the study
The presence of ovarian disorders (due to irregular menstruation and mood disorders caused by it)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The physical symptoms of premenstrual syndrome. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: Premenstrual Symptoms Tool (Rossignol & Bonlander).
Secondary Outcome Measures
NameTimeMethod
Mood symptoms of premenstrual syndrome. Timepoint: Before the intervention three months after the last counseling. Method of measurement: Premenstrual Symptoms Tool (Rossignol & Bonlander).
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