Determining the effect of vitamin D3 and positive group counseling with lifestyle changes in premenstrual women of reproductive age

Phase 3

• Conditions: Women's premenstrual syndrome.; Premenstrual tension syndrome; N94.3

• Registration Number: IRCT20191231045967N1
• Lead Sponsor: Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 June 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 84

Inclusion Criteria

Being a resident of Rafsanjan city
No history of treatment or depression or anxiety disorder
No history of treatment or eating disorder
No history of treatment or anemia disorder
No history of treatment or thyroid disorder
No history of treatment or presence of diabetes
Not taking birth control pills for medical reasons
Not taking any herbal medicine or medicine that affects premenstrual syndrome
Lack of treatment with psychiatric drugs and other non-pharmacological methods
Lack of treatment with other non-medicinal methods
Having two consecutive menstrual cycles a year with symptoms of premenstrual syndrome with at least five symptoms, one of which are mood disorders, which begin in the second half of the menstrual cycle and improve after menstruation, according to the self-report.
Having at least a 30% increase in symptom severity within 5 days before menstruation based on the PMS
Willingness to continue collaborating on tasks for 6 weeks
Failure to participate in another related study until the expiration of the current study

Exclusion Criteria

Severe form of premenstrual syndrome with a score of 35 and more from the premenstrual syndrome calendar

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1-Mean premenstrual syndrome scores, 2- Satisfaction with intervention methods. Timepoint: 1-?For premenstrual syndrome before the intervention, complete the sixth week of the intervention and finish the tenth week.2- At the end of 6 and 10 weeks. Method of measurement: 1-Premenstrual Syndrome Screening Tool , 2-Satisfaction tool.