NCT07571603

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 19, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 19, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

April 13, 2026

Completed
23 days until next milestone

First Posted

Study publicly available on registry

May 6, 2026

Completed
Last Updated

May 6, 2026

Status Verified

April 1, 2026

Enrollment Period

4 months

First QC Date

April 13, 2026

Last Update Submit

April 30, 2026

Conditions

Keywords

Reformer PilatesExerciseFunctional CapacityHealthy Women

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

EXPERIMENTAL

Participants received supervised reformer pilates exercises twice a week for 8 weeks.

Behavioral: Reformer Pilates Exercise

Control Group

OTHER

Participants followed a home-based exercise program twice a week for 8 weeks without supervised reformer pilates.

Behavioral: Home-Based Exercise

Interventions

Participants performed a home-based exercise program on their own for 8 weeks.

Control Group

Participants performed supervised reformer pilates exercises twice a week for 8 weeks.

Reformer Pilates Group

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly female participants were included in this study.
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Istanbul Aydin University- FLC Concept Healthy Living Center

Istanbul, Istanbul, 34000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Ayca S Sensoy, PT, MSc Student

    Istanbul Aydın University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants were randomly assigned to either the intervention (reformer pilates) group or the control group.
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.

Locations