Pilates vs. Aerobic Exercises: Impact on Primary Dysmenorrhea
This study aims to compare the effects of Pilates and aerobic exercises as treatments for reducing pain and improving quality of life in women experiencing primary dysmenorrhea.
Pilates exercises
+ Aerobic exercises
Treatment Study
Summary
Study start date: December 1, 2025
Actual date on which the first participant was enrolled.Primary dysmenorrhea, a condition characterized by painful menstrual cramps, often disrupts daily activities and quality of life in many young women. This study focuses on comparing two non-pharmacological interventions, Pilates exercises and aerobic exercises, to manage this menstrual pain. These exercise-based approaches are considered safe and effective, but there is limited information on which one works better. In this study, participants with primary dysmenorrhea are divided into two groups. Group A will engage in a structured Pilates exercise program, which includes controlled movements to enhance core stability, flexibility, breathing control, and muscle strength. These sessions will occur three times a week for eight weeks, each lasting around 30 minutes. Group B will participate in a supervised aerobic exercise program, consisting of rhythmic and continuous movements to boost cardiovascular endurance. These sessions will also take place three times a week for eight weeks, each lasting approximately 40 minutes. The goal is to evaluate changes in menstrual pain severity and quality of life before the start of the intervention and after completing the eight-week exercise program. The study's findings aim to provide evidence on the comparative effectiveness of Pilates and aerobic exercises in managing primary dysmenorrhea.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.32 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment 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 not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy 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
Delta university, Faculty of Physical Therapy
Al Mansurah, EgyptOpen Delta university, Faculty of Physical Therapy in Google Maps