- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07358091
Investigation of Flexibility, Strength, and Posture in Women Practicing Reformer Pilates Across Different Age Groups
March 25, 2026 updated by: hazal genc, Istanbul Medipol University Hospital
Investigation of Flexibility, Strength, and Posture in Women Practicingr Reformer Pilates Across Different Age Groups
"Investigation of Flexibility, Strength, and Posture in Women Practicing Regular Reformer Pilates Across Different Age Groups"
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
"Investigation of Flexibility, Strength, and Posture in Women Practicing Regular Reformer Pilates Across Different Age Groups"
Study Type
Interventional
Enrollment (Actual)
38
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Istanbul, Turkey (Türkiye), 34070
- Bahceşehir University Health Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria
- Female participants aged 18-65 years
- Regular participation in Reformer Pilates exercises
- Voluntary participation with signed informed consent
- No medical condition preventing participation in the assessment and testing procedures
Exclusion Criteria
- Pregnancy
- History of spinal surgery within the last 6 months
- Presence of neurological conditions affecting mobility (e.g., Parkinson's disease)
- Presence of chronic systemic diseases (e.g., cancer, diabetes)
- Severe pain-related movement limitation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Reformer Pilates
reformer pilates- 46-60 age
|
Reformer Pilates is a low-impact exercise method performed using spring-based equipment that aims to improve muscle strength, flexibility, core stability, and postural control in women aged 18-46 through controlled and precise movements.
|
|
Experimental: reformer pilates
reformer pilates- 18-45 age
|
Reformer Pilates is a low-impact exercise method performed using spring-based equipment that aims to improve muscle strength, flexibility, core stability, and postural control in women aged 18-46 through controlled and precise movements.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flexibility Assessment
Time Frame: 5 weeks
|
Flexibility was assessed using the Sit-and-Reach Test
|
5 weeks
|
|
Sørensen Test
Time Frame: 5 weeks
|
This test is a widely used and reliable method for assessing the isometric endurance of the erector spinae muscles
|
5 weeks
|
|
Trunk Flexor Endurance Test
Time Frame: 5 weeks
|
Participants were positioned in a seated posture with the trunk inclined at 60°, the knees flexed at 90°, and the arms placed either across the chest or behind the head.
Participants were instructed to maintain their trunk at this angle for as long as possible, and the endurance time was recorded in seconds using a stopwatch.
This test was conducted to assess the isometric endurance of the trunk flexor muscles, particularly the rectus abdominis and iliopsoas muscles
|
5 weeks
|
|
Lateral Bridge (Side Bridge) Test
Time Frame: 5 weeks
|
Participants were positioned in a side-lying posture, supporting their body on the lower arm and the lateral aspect of the feet, maintaining the trunk in a straight line.
The upper arm was placed on the hip, and participants were instructed to hold this position for as long as possible.
The endurance time was recorded in seconds using a stopwatch.
This test is a commonly used method to assess the isometric endurance of the oblique muscle groups and the quadratus lumborum muscles
|
5 weeks
|
|
Muscle Strength and Body Composition Assessments
Time Frame: 5 weeks
|
In this study, the Visbody 3D body analysis system was used to evaluate participants' body composition and postural characteristics through millimetric three-dimensional scanning.
The system provided segmental muscle mass analysis for the upper extremities, lower extremities, and trunk, enabling a detailed assessment of the relationship between muscle distribution and strength and endurance outcomes.
In addition to body composition parameters such as body fat, fat-free mass, BMI, and visceral fat, postural variables including spinal alignment, shoulder and pelvic symmetry, pelvic tilt, and shoulder joint angles (abduction and flexion) were assessed.
Overall, Visbody supplied comprehensive, multidimensional data that supported functional test results and enhanced measurement reliability.
|
5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 6, 2025
Primary Completion (Actual)
January 20, 2026
Study Completion (Actual)
February 20, 2026
Study Registration Dates
First Submitted
January 13, 2026
First Submitted That Met QC Criteria
January 13, 2026
First Posted (Actual)
January 22, 2026
Study Record Updates
Last Update Posted (Actual)
March 31, 2026
Last Update Submitted That Met QC Criteria
March 25, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- E-78097791-0204927
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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