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Clinical Trials/NCT02809066
NCT02809066
Completed
Not Applicable

Effect of Sufficient Dietary Calcium Intake in Women With Premenstrual Syndrome

Eastern Mediterranean University1 site in 1 country31 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Premenstrual Syndrome
Sponsor
Eastern Mediterranean University
Enrollment
31
Locations
1
Primary Endpoint
Change in Premenstrual Syndrome Scale (PMSS)
Status
Completed
Last Updated
9 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
January 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Merve YURT

Senior Instructor

Eastern Mediterranean University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in Premenstrual Syndrome Scale (PMSS)

Time Frame: Eight weeks

Premenstrual Syndrome Scale (PMSS) was used for symptom assessment at initial and after two menstrual cycles.

Secondary Outcomes

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

Study Sites (1)

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