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Dietary Calcium Intake in Premenstrual Syndrome

Effect of Sufficient Dietary Calcium Intake in Women With Premenstrual Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02809066
Enrollment
31
Registered
2016-06-22
Start date
2015-01-31
Completion date
2016-01-31
Last updated
2016-06-22

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

Conditions

Premenstrual Syndrome

Keywords

premenstrual syndrome, calcium, quality of life

Brief summary

This study was planned and conducted to investigate effect of adequate calcium intake on Premenstrual Syndrome (PMS) symptoms in women with PMS who have inadequate calcium intake.

Detailed description

This study was planned and conducted to investigate effect of adequate calcium intake on Premenstrual Syndrome (PMS) symptoms in women with PMS who have inadequate calcium intake. Thirty one women, aged between 20-28 years, diagnosed with PMS and suitable for inclusion criteria, were participated in study. Participants were allocated to intervention (n=16) and control (n=15) groups randomly.

Interventions

OTHERSufficient dietary calcium intake in premenstrual syndrome

Intervention group was ensured to take at least 1000 mg calcium from foods, 700-800 mg of it from dairy and dairy products, according to Recommended Dietary Allowances (RDA), for two months. These foods were; * 50 gr kashkaval cheese, * 400 ml milk and * 150 gr yogurt for each day.

Sponsors

Eastern Mediterranean University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 28 Years
Healthy volunteers
No

Inclusion criteria

Women with; * PMS who have inadequate calcium intake * Regular menstrual cycle * Menstrual flow which occurs every 22 to 35 days and last three to eight days

Exclusion criteria

* Having any of metabolic diseases * Use oral contraceptive pill * user vitamins and minerals supplements * being smoker

Design outcomes

Primary

MeasureTime frameDescription
Change in Premenstrual Syndrome Scale (PMSS)Eight weeksPremenstrual Syndrome Scale (PMSS) was used for symptom assessment at initial and after two menstrual cycles.

Secondary

MeasureTime frame
Change in Quality of life scale Short Form (SF-36)Eight weeks

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026