The Effect of Kegel Exercise on Menstruation Symptom, Severity of Dysmenorrheic Symptoms and Quality of Life in Nursing Students With Primary Dysmenorrhea: A Randomized Controlled Study
Kegel Exercise
Behavior
+ Motor Activity
Supportive Care Study
Summary
Study start date: March 1, 2021
Actual date on which the first participant was enrolled.This study focuses on evaluating the impact of Kegel exercises on menstrual symptoms, the severity of pain associated with dysmenorrhea, and overall quality of life in nursing students who experience primary dysmenorrhea, which is a common and painful menstrual condition. Kegel exercises are simple pelvic floor exercises that may help reduce menstrual pain and improve daily functioning. This research aims to determine if performing these exercises regularly can provide relief from symptoms and enhance the quality of life for those affected, addressing an unmet need for more effective, non-pharmaceutical intervention options. Participants in this study are divided into two groups: one group receives online training for Kegel exercises and is reminded to perform them three times daily, while the other group does not receive any intervention. The study measures outcomes by comparing pain levels, menstrual symptoms, and quality of life between the two groups. The research hypothesizes that those who perform Kegel exercises will experience less pain and improved quality of life compared to those who do not, potentially offering a simple and accessible method to manage dysmenorrhea symptoms.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.89 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 25 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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.This study has 1 location
Gümüşhane University, Faculty of Health Sciences, Department of Nursing
Gümüşhane, Turkey (Türkiye)Open Gümüşhane University, Faculty of Health Sciences, Department of Nursing in Google Maps