Effects of Reformer Pilates on Adolescents' Posture and Trunk Endurance

April 8, 2025 updated by: Muhammed Şeref Yıldırım, Trakya University

The Effects of Reformer Pilates Exercises on Trunk Endurance, Posture, and Body Awareness in Adolescents

This study aims to investigate the effects of reformer pilates exercises on posture, core endurance, and body awareness in adolescents. The hypothesis is that reformer pilates will improve these outcomes compared to a control group receiving only informational support. Participants will be randomized into two groups and assessed over six weeks.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This randomized controlled trial investigates the effects of reformer pilates exercises on core endurance, posture, and body awareness in adolescents aged 10-19. Participants will be randomly assigned to one of two groups: an intervention group performing reformer pilates exercises and a control group receiving educational information on posture and physical activity. Both groups will be assessed at baseline and after the 6-week intervention period.

A. Study Design

Intervention Group: Participants in this group will perform reformer pilates exercises twice a week for six weeks. The exercises will target both deep and superficial core muscles and focus on improving posture and body awareness. The program will include progressive adjustments to resistance and repetitions every two weeks.

Control Group: Participants in this group will receive educational sessions about proper posture and physical activity but will not engage in pilates exercises. They will have the option to participate in the pilates program after the study is completed.

B.Outcome Measures B.1. Trunk Endurance Extensor Endurance (Sorensen Test): Assesses the endurance of trunk extensor muscles by recording the duration the participant can hold a horizontal position against gravity.

Flexor Endurance Test: Measures the endurance of trunk flexor muscles by timing how long the participant can maintain a 60° flexion position.

B.2. Posture Analysis Postural alignment will be assessed using the Artificial Intelligence Posture Evaluation and Correction System (APECS) software, a photogrammetric tool for posture evaluation.

Markers will be placed on specific anatomical landmarks (e.g., ears, shoulders, hips, and knees) in static standing and sitting positions.

Photographs will be taken from the front, side, and back views to analyze:

Sagittal plane deviations (e.g., forward head posture, thoracic kyphosis). Frontal plane asymmetries (e.g., shoulder or pelvic tilts). Sitting posture deviations (e.g., cervical angle or slouched sitting positions).

Data will include angles and alignment deviations to quantify changes after the intervention.

B.3. Body Awareness Body Awareness Questionnaire (BAQ): Evaluates body awareness across physical, emotional, and social dimensions.

Objectified Body Consciousness Scale (OBCS): Measures dimensions of body monitoring, body shame, and appearance control beliefs.

C. Statistical Analysis Relationships between variables: Pearson's correlation coefficient will be used for normally distributed data, and Spearman's rank correlation will be applied for non-normally distributed data.

Between-group comparisons: The Independent Samples t-Test will be used for normally distributed data, and the Mann-Whitney U Test will be applied for non-parametric data.

Within-group comparisons: Paired t-Tests will be conducted for normally distributed data, and the Wilcoxon Signed Rank Test will be used for non-parametric data to assess changes from pre- to post-intervention.

Significance Level: All statistical analyses will be performed using the SPSS software package (version 26.0), with a significance level set at p < 0.05.

Study Type

Interventional

Enrollment (Estimated)

26

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 Contact

Study Locations

    • İskender
      • Edirne, İskender, Turkey, 22100
        • Recruiting
        • Trakya University
        • Contact:

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged between 10-19 years.
  • Voluntary participation with signed informed consent.
  • Ability to read and write in Turkish.

Exclusion Criteria:

  • History of orthopedic injury within the last 3 months.
  • Obesity (BMI > 30 kg/m²).
  • Being under follow-up for a scoliosis diagnosis.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Reformer Pilates Group

Participants in this group will perform reformer pilates exercises twice weekly for six weeks. Each session will last 50 minutes and include warm-up, main exercises, and cool-down phases.

The exercises will target both deep and superficial core muscles, focusing on core endurance, posture, and body awareness.

The main program includes 12 reformer exercises (e.g., Footwork Series, Pelvic Lift, Arm Circles, Leg Circles) with progressive resistance and repetitions (10 repetitions for the first 3 weeks and 15 repetitions for the last 3 weeks).

The intervention will be carried out under professional supervision. Cool-down includes diaphragmatic breathing and relaxation-focused Footwork exercises.

This intervention involves a structured reformer pilates program designed to enhance core endurance, posture, and body awareness. The program includes exercises such as Footwork Series, Pelvic Lift, Arm Circles, Leg Circles, Frog Series, Long Box Series, Short Box Series, Elephant, Knee Stretch Series, Stomach Massage, and Side Stretch. The program emphasizes progressive resistance, controlled movements, and professional supervision to ensure safety and effectiveness. Sessions are conducted twice weekly for six weeks.
No Intervention: Educational Session Group

Participants in this group will receive a one-time, 60-minute educational session on proper posture and the importance of physical activity at the start of the study. This session will include:

Verbal and visual explanations about maintaining correct postural alignment in daily activities such as sitting, standing, and lifting.

Practical tips on integrating physical activity into their daily routines to support overall health and posture.

No structured exercise or physical activity will be performed during the six-week study period. Participants will be invited to post-intervention assessments after six weeks. Additionally, participants will be offered the opportunity to join the reformer pilates exercise program after the study concludes, if they wish.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural Alignment
Time Frame: Baseline and 6 weeks post-intervention.
Evaluation of static postural alignment using the Artificial Intelligence Posture Evaluation and Correction System (APECS). Photos taken from front, side, and back will be analyzed to assess sagittal and frontal plane deviations, including cervical angle, shoulder alignment, and spinal curvature.
Baseline and 6 weeks post-intervention.
Trunk Endurance
Time Frame: Baseline and 6 weeks post-intervention.
Assessment of core endurance using the Sorensen Test for trunk extensor muscles and the Flexor Endurance Test for trunk flexor muscles. The duration (in seconds) that participants can maintain the test position will be recorded.
Baseline and 6 weeks post-intervention.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Objectified Body Consciousness Scale ( OBSC)
Time Frame: Baseline and 6 weeks post-intervention.
Evaluation of body monitoring, body shame, and appearance control beliefs using the OBCS. Scores are calculated for each subscale individually.
Baseline and 6 weeks post-intervention.
Body Awareness Questionnaire (BAQ)
Time Frame: Baseline and 6 weeks post-intervention.
Assessment of body awareness across emotional, physical, and social dimensions using the Body Awareness Questionnaire. Higher scores indicate better body awareness.
Baseline and 6 weeks post-intervention.

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)

March 1, 2025

Primary Completion (Estimated)

October 7, 2025

Study Completion (Estimated)

October 7, 2025

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

January 6, 2025

First Posted (Actual)

January 9, 2025

Study Record Updates

Last Update Posted (Actual)

April 11, 2025

Last Update Submitted That Met QC Criteria

April 8, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • TU-FTR-MŞY-003

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

product manufactured in and exported from the U.S.

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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