- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06767228
Effects of Reformer Pilates on Adolescents' Posture and Trunk Endurance
The Effects of Reformer Pilates Exercises on Trunk Endurance, Posture, and Body Awareness in Adolescents
Study Overview
Status
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zeynep Arıbaş, PhD
- Phone Number: +905057443650
- Email: zozaydin@gmail.com
Study Locations
-
-
İskender
-
Edirne, İskender, Turkey, 22100
- Recruiting
- Trakya University
-
Contact:
- Hilal Keklicek
- Phone Number: +905447208798
- Email: hhotaman23@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- TU-FTR-MŞY-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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