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Comparing the effect of relaxation and vitamin B6 on pre-menstrual syndrome

Phase 2
Conditions
Premenstrual Syndrome.
Premenstrual tension syndrome
N.94.3
Registration Number
IRCT2014070518357N1
Lead Sponsor
Vice Chancellor for research of Rafsanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
250
Inclusion Criteria

Age 25 to 18 years; Normal menstruation (bleeding interval: 3 to 8 days and during cycle: 26 to 31 days); Single; no history of mental illness and depression; No history of use antidepressants and hormones drug; Did not have any event in past two months

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Premenstrual Syndrome Symptoms. Timepoint: Before the intervention and 3 months after intervention with monthly. Method of measurement: DSM-IV Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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