Comparison Between Pilates Exercises and Aerobic Exercises in Primary Dysmenorrhea
1 other identifier
interventional
32
1 country
1
Brief Summary
Comparison between Pilates exercises and aerobic exercises in primary dysmenorrhea
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2025
CompletedFirst Submitted
Initial submission to the registry
December 15, 2025
CompletedFirst Posted
Study publicly available on registry
December 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 12, 2026
CompletedFebruary 17, 2026
February 1, 2026
2 months
December 15, 2025
February 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
menstrual pain severity
Pain intensity will be measured using the Visual Analog Scale (VAS) atbaseline and after 8 weeks of Pilates or aerobic exercises.low score zero pain and high score 10 worst pain imaginable
8 week
Secondary Outcomes (1)
Change quality of life
8weeks
Other Outcomes (1)
The Verbal Multidimensional Scoring System (VMSS)
8weeks
Study Arms (2)
Pilates exercises
EXPERIMENTALPatients will receive Pilates exercise, the exercise program was repeated 3 times 8 weeks 30 minute for each leg in session. Focused on core strengthening, flexibility, and breathing exercises to alleviate menstrual pain."
Aerobic exercises
ACTIVE COMPARATORPatients will receive aerobic exercise, the exercise program was repeated 3 times 8 weeks 40minute for each session. Including walk-ing and treadmill
Interventions
Patients will receive Pilates exercise, the exercise program was repeated 3 times 8 weeks 30 minute for each leg in session. focuses on core strengthening, flexibility, and breathing techniques designed to reduce menstrual pain and improve overall physical well-being.
Patients will receive aerobic exercise, the exercise program was repeated 3 times 8 weeks 40minute for each session. Including walk-ing and treadmill
Eligibility Criteria
You may qualify if:
- Females diagnosed with primary dysmenorrhea
- Age between 18 and 25 years
- Regular menstrual cycle (28-35 days)
- Body mass index (BMI) between 18.5 and 24.9 kg/m²
You may not qualify if:
- Presence of any acute or chronic pelvic pathology
- History of regular exercise participation (≥3 days per week, average 30-45 minutes per day)
- Participation in structured physical activities such as swimming, running, or fitness center training
- Inability to perform exercise
- Unwillingness to participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Delta university, Faculty of Physical Therapy
Al Mansurah, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Participants and instructors are not blinded. Inclusion Criteria: 1. Females with Primary dysmenorrhea 2. Age between 18 to 25 years 3. Having regular menstrual cycle of 28 - 35 days 4. Individual with BMI 18.5 to 24.9 kg/m2 Exclusion Criteria: 1. Acute or chronic pelvic pathology 2. Subjects having any history of regular exercises 3days/week \[daily average 30-45 min\] 3. Attending physical activity like swimming, running or fitness center 4. Who cannot perform exercise 5. Not willing to participate
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 15, 2025
First Posted
December 29, 2025
Study Start
December 1, 2025
Primary Completion
February 10, 2026
Study Completion
February 12, 2026
Last Updated
February 17, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
The study involves a small number of participants, and there is no plan to share individual participant data to ensure privacy and confidentiality.