EFFECTS OF REFORMER PILATES ON FUNCTIONAL CAPACITY AND QUALITY OF LIFE IN WOMEN
THE EFFECTS OF REFORMER PILATES EXERCISES APPLIED IN WOMEN ON FUNCTIONAL CAPACITY, HEART RATE, BODY COMPOSITION AND QUALITY OF LIFE
1 other identifier
interventional
50
1 country
1
Brief Summary
This study aims to investigate the effects of reformer pilates exercises on functional capacity, heart rate, body composition, and quality of life in women. A total of 50 participants were initially enrolled; however, 44 participants completed the study. Participants were divided into intervention and control groups, and the intervention group performed reformer pilates exercises for 8 weeks.
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 Nov 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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 19, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 19, 2026
CompletedFirst Submitted
Initial submission to the registry
April 13, 2026
CompletedFirst Posted
Study publicly available on registry
May 6, 2026
CompletedMay 6, 2026
April 1, 2026
4 months
April 13, 2026
April 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Functional Capacity (6-Minute Walk Test)
Functional capacity will be assessed using the 6-minute walk test (6MWT). The distance walked in meters (m) will be recorded.
At baseline and after 8 weeks
Secondary Outcomes (6)
Quality of Life (Short Form-12, SF-12)
At baseline and after 8 weeks
Body Fat Percentage (%)
At baseline and after 8 weeks
Heart Rate (beats per minute, bpm)
At baseline and after 8 weeks
Skeletal Muscle Mass (kg)
At baseline and after 8 weeks
Body Weight (kg)
At baseline and after 8 weeks
- +1 more secondary outcomes
Study Arms (2)
Reformer Pilates Group
EXPERIMENTALParticipants received supervised reformer pilates exercises twice a week for 8 weeks.
Control Group
OTHERParticipants followed a home-based exercise program twice a week for 8 weeks without supervised reformer pilates.
Interventions
Participants performed a home-based exercise program on their own for 8 weeks.
Participants performed supervised reformer pilates exercises twice a week for 8 weeks.
Eligibility Criteria
You may qualify if:
- Female participants aged between 20 and 40 years
- Healthy individuals capable of performing exercise
- Voluntary participation in the study
- Ability to attend Pilates sessions regularly
You may not qualify if:
- Male participants
- Receiving any form of physical therapy intervention
- History of surgery
- Severe spinal pathologies
- Neurological disorders
- Cardiopulmonary diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ayca Sena Sensoylead
Study Sites (1)
Istanbul Aydin University- FLC Concept Healthy Living Center
Istanbul, Istanbul, 34000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ayca S Sensoy, PT, MSc Student
Istanbul Aydın University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Physiotherapist, Graduate Student (MSc)
Study Record Dates
First Submitted
April 13, 2026
First Posted
May 6, 2026
Study Start
November 1, 2025
Primary Completion
February 19, 2026
Study Completion
February 19, 2026
Last Updated
May 6, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy and ethical considerations.