Effects of Reformer Pilates on Adolescents' Posture and Trunk Endurance
NCT ID: NCT06767228
Last Updated: 2025-04-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
26 participants
INTERVENTIONAL
2025-03-01
2025-10-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of Pilates on Posture and Physical Fitness Parameters in 5-6 Years Old Children
NCT05210426
Posture Training for Middle Schoolers
NCT06909747
The Effects of Core Stabilization Exercises on Balance, Trunk Muscle Endurance and Posture on Sedentary Individuals
NCT05970523
Trunk Proprioception in Adolescent Idiopathic Scoliosis
NCT05326256
Muscle Fatigue and Foot Biomechanics
NCT03607253
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
Reformer Pilates
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.
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.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Reformer Pilates
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Voluntary participation with signed informed consent.
* Ability to read and write in Turkish.
Exclusion Criteria
* Obesity (BMI \> 30 kg/m²).
* Being under follow-up for a scoliosis diagnosis.
10 Years
19 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Trakya University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Muhammed Şeref Yıldırım
Research Assistant (PhD)
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Trakya University
Edirne, İskender, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TU-FTR-MŞY-003
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.