- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06966648
- Original Trial
Pilot Study on Core Stabilization Training on Stable vs Unstable Surfaces in Young Rhythmic Gymnasts
July 14, 2025 updated by: Dimitrios Lytras, International Hellenic University
Effect of Core Stabilization Training on Balance and Pivot Performance in Young Rhythmic Gymnasts: A Pilot Randomized Controlled Trial
This pilot randomized controlled trial will investigate the effects of a 7-week core stabilization program performed on stable versus unstable surfaces in young competitive rhythmic gymnasts.
Sixteen athletes will be randomized into two groups and will be assessed for changes in static balance and pivot performance.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Rhythmic gymnastics requires high-level neuromuscular control, especially for skills involving balance and rotation.
Core stabilization exercises are commonly included in training, but limited evidence exists regarding the impact of surface type on training effectiveness.
This pilot study will compare the effects of a 7-week core stabilization program conducted on stable versus unstable surfaces on balance and pivot execution in rhythmic gymnasts aged 7-12.
Participants will be randomly allocated into two equal groups and will be assessed pre- and post-intervention on selected balance and pivot tasks in accordance with Fédération Internationale de Gymnastique (FIG) standards.
The study aims to inform future trials by estimating effect sizes and assessing the feasibility of the protocol.
Study Type
Interventional
Enrollment (Actual)
16
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 Locations
-
-
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Thessaloniki, Greece, 57400
- International Hellenic University
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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
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Female rhythmic gymnasts aged 7 to 12 years
- Minimum of 1 year of experience in rhythmic gymnastics
- Active participation in organized training at least 3 times per week
- No current musculoskeletal pain or injury
- Ability to perform all training and assessment tasks safely
- Written informed consent provided by a parent or legal guardian
Exclusion Criteria:
- History of acute lower limb or spinal injury within the past 6 months
- Presence of neurological, orthopedic, or vestibular disorders affecting balance
- Concurrent participation in other structured physical training programs outside rhythmic gymnastics
- Any medical condition that would contraindicate participation in physical exercise
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Stable Surface Group
Participants will perform a core stabilization program on stable surfaces (e.g., floor, foam blocks).
Exercises target trunk control and balanc
|
Participants will perform a structured core stabilization training program on stable surfaces, such as the floor and rigid foam blocks.
The program includes functional exercises targeting trunk control, postural alignment, and balance, delivered three times per week over a 7-week period.
|
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Experimental: Unstable Surface Group
Participants will perform the same core stabilization program on unstable surfaces (e.g., BOSU, wobble board).
|
Participants will perform the same structured core stabilization training program as the stable surface group, but on unstable surfaces such as BOSU balls and wobble boards.
The intervention is designed to challenge balance, proprioception, and core muscle activation.
Sessions are conducted three times per week over a 7-week period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance Duration
Time Frame: Baseline and Week 7 (post-intervention)
|
Balance performance will be measured in seconds using a handheld stopwatch (Ultrak 250 Stopwatch Chronometer).
Each gymnast will perform three static balance elements (passé, attitude, and side split with help) in relevé position while wearing half shoes.
The timer will start once the gymnast achieves final posture and stop when balance is lost, form deteriorates, or the center of gravity shifts.
Five trials will be performed for each element, and the longest successful attempt will be recorded.
All tests will be performed with eyes open.
|
Baseline and Week 7 (post-intervention)
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|
Pivot Performance (Number of Clean Rotations)
Time Frame: Baseline and Week 7 (post-intervention)
|
Pivot performance will be assessed as the number of clean, full rotations executed without technical faults, based on Fédération Internationale de Gymnastique (FIG) regulations.
Each gymnast will perform two pivot elements (passé forward and attitude) in relevé position while wearing half shoes, maintaining proper form and control.
Five attempts will be performed for each pivot type, and the highest number of clean rotations will be recorded.
All tests will be performed with eyes open.
|
Baseline and Week 7 (post-intervention)
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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)
May 5, 2025
Primary Completion (Actual)
July 15, 2025
Study Completion (Actual)
July 15, 2025
Study Registration Dates
First Submitted
May 4, 2025
First Submitted That Met QC Criteria
May 4, 2025
First Posted (Actual)
May 13, 2025
Study Record Updates
Last Update Posted (Actual)
July 17, 2025
Last Update Submitted That Met QC Criteria
July 14, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- EC-11 2025
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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