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A healthy diet and premenstrual syndrome

Phase 3
Conditions
premenstrual syndrome.
premenstrual syndrome
N94.3
Registration Number
IRCT20201129049526N1
Lead Sponsor
application for fund was done and still awaiting approval
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
70
Inclusion Criteria

Adolescents who are at grade 10 or 11, aged 16 years to 19 years old, and have regular menstrual cycles will be included in the study

Exclusion Criteria

known to have psychiatric disorders (such as depression, generalized anxiety disorder, post-traumatic stress disorder, psychotic disorders), diabetes, thyroid disease, oral contraceptive use, herbal remedy use for PMS symptoms, and those who have had dietary advice before for PMS symptoms.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The improvements in the severity of premenstrual symptoms. Timepoint: At baseline and 2 months after intervention. Method of measurement: Daily Record of Severity of Problem (Arabic version).
Secondary Outcome Measures
NameTimeMethod
Improvements in quality of life. Timepoint: at baseline and at the end of 2 months of starting the intervention. Method of measurement: The medical outcome study short form-36 (SF-36) and Perceived stress scale PSS.
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