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Clinical Trials/NCT05290181
NCT05290181
Completed
Not Applicable

The Effect of Pilates Exercise and Whatsapp Text-Based Support Program on Premenstrual Syndrome (PMS) Symptoms: A Randomized Controlled Study

Aydin Adnan Menderes University1 site in 1 country68 target enrollmentJanuary 12, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Premenstrual Syndrome
Sponsor
Aydin Adnan Menderes University
Enrollment
68
Locations
1
Primary Endpoint
Premenstrual syndrome scale (PMSS)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of this study is to evaluate the effect of Pilates exercise and Whatsapp text message-based support program on PMS symptoms experienced by university female students.

Detailed Description

In this study, it will be answered whether the Pilates exercise and the support program based on Whatsapp text messages have an effect on the PMS symptoms experienced by university female students. Demographic information of the participants will be collected with the Personal Information form. The personal information form is a form prepared by the researchers with the support of the literature, consisting of 21 questions aiming to obtain information about the socio-demographic characteristics, menstrual characteristics, and lifestyle behaviors of the students. PMS symptoms will be evaluated with the Premenstrual Syndrome Scale. First of all, the premenstrual syndrome scale will be applied by trying to reach all 380 female students studying at the school. Afterward, 68 students with PMS who meet the inclusion criteria will be divided into 34 intervention and 34 control groups by simple randomization. In order to prevent interaction between the intervention and control group students in the randomization, the places where the students stay (home, dormitory rooms) will be taken into account. A support program including pilates exercise and WhatsApp text messages will be applied to the initiative group for 8 weeks. No attempt will be made on the control group.

Registry
clinicaltrials.gov
Start Date
January 12, 2022
End Date
June 5, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Aydin Adnan Menderes University
Responsible Party
Principal Investigator
Principal Investigator

Ayca Balmumcu

Principal Investigator, Women's health and obstetrics nursing

Aydin Adnan Menderes University

Eligibility Criteria

Inclusion Criteria

  • Having regular menstrual cycles (intervals of 21-35 days, lasting 3-10 days),
  • Body mass index of 18.5-24.9 kg/m. to be between
  • Absence of chronic disease,
  • Absence of a hormonal disease such as polycystic ovary syndrome,
  • Using smart mobile phone
  • Not using oral contraceptives or antidepressants.

Exclusion Criteria

  • - Having a chronic or physical illness that prevents Pilates.

Outcomes

Primary Outcomes

Premenstrual syndrome scale (PMSS)

Time Frame: Baseline

The premenstrual syndrome scale (PMSS) aims to measure the severity of symptoms. The scale consists of 44 items in 5-point Likert type. The Cronbach's alpha value of the scale was determined as 0.75. As stated in the PMSS directive, while filling out the scale, the participants should mark according to the symptoms they felt one week before the period. In scoring the scale, the "Never" option is 1 point, the "Very little" option is 2 points, the "Sometimes" option is 3 points, the "Frequently" option is 4 points, and the "Constantly" option is evaluated. as 5 points. While evaluating the PMSS results, the presence of PMS is evaluated according to the condition of passing 50% of the highest score that can be obtained from the total and subscale scores. The highest possible score for the total score is 220, 50% of which is 110. A score above 110 points on the scale indicates the presence of PMS.

Secondary Outcomes

  • Premenstrual syndrome scale (PMSS)(Immediately after the 8-week support intervention program)

Study Sites (1)

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