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

Survey the effect of vitamin D3 tablet intake, positivism group consulting with changing in life style in the treatment of premenstrual syndrome in women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191231045967N1
Enrollment
84
Registered
2020-02-11
Start date
2020-02-20
Completion date
Unknown
Last updated
2021-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Women's premenstrual syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Intervention group: Intervention group consuming vitamin D3, with a criterion and after determining 25 hydroxyvitamin D level, subjects with serum level less than 30 ng / ml will be in

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Tahmineh Faraj Khoda

Yazd University of Medical Sciences

maryam.mahmoodi8874@gmail.com009843527244

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026