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Acupressure Mat for Stress, Sleep, and Premenstrual Symptoms in Students

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What is being tested

Acupresure mat

+ Basic mat

Other
Who is being recruted

+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Placebo-Controlled
Interventional
Study Start: November 2024
See protocol details

Summary

Principal SponsorGulhane School of Medicine
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 15, 2024

Actual date on which the first participant was enrolled.

This study investigates how using an acupressure mat can affect stress levels, sleep quality, and premenstrual symptoms in students who experience premenstrual syndrome (PMS). PMS can cause a variety of physical and emotional symptoms that occur before a woman's menstrual period, often impacting daily life. By targeting students with PMS, this research aims to explore whether an acupressure mat can provide a natural and non-invasive way to alleviate these symptoms, potentially offering a new method to improve well-being and quality of life for those affected. Participants in the study will be randomly assigned to use either an acupressure mat or a plain mat. The acupressure mat is intended to be used while lying down, allowing its small, raised points to apply pressure to the body, which is believed to help relieve stress and improve sleep. Researchers will measure the severity of premenstrual symptoms, perceived stress, and sleep quality both before and after the study period to determine if there are any notable changes. The study does not specify any potential risks, as the focus is on comparing the effects of the two types of mats.

Official TitleExamining the Effect of Acupressure Mat on Perceived Stress, Sleep Quality and Premenstrual Symptoms in Students Experiencing Premenstrual Syndrome: Randomized Controlled Study
Principal SponsorGulhane School of Medicine
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

42 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Female

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

3 inclusion criteria required to participate
Using medication and/or non-medical methods to cope with PMS

Having any gynecological disease (abnormal uterine bleeding, myoma, ovarian cyst, etc.)

Using contraceptive medication.

4 exclusion criteria prevent from participating
Participants wanting to withdraw from the study at any stage of the study

Participants not complying with the research plan

Diagnosed with a psychiatric or gynecological disease during the study

Participants starting to receive additional treatment for PMS during the study period

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
They will be asked to lie on the acupressure mat for 15 minutes once a day, 3 days a week (Monday, Wednesday, Friday). A reminder message will be sent on the morning of the application so that participants do not forget and are motivated. After each application, participants will be asked to fill out the session monitoring chart.

Group II

Placebo
Students will be given a placebo exercise on a flat yoga/exercise mat on the same days, in the same way and for the same duration as the intervention group.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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