- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07288645
Enhancing Stability and Jumping Skills Through Combined Static and Dynamic Balance Training in Female Chinese University-Level Gymnastics Beginners
February 1, 2026 updated by: Yi Wang
This study aims to investigate the effects of different balance training programs (dynamic, static, combined dynamic and static) on the stability, jumping skills, and gymnastic movement skills of female university students who are beginners in gymnastics.
Participants will be randomly divided into four groups: the first group will receive dynamic balance training (including exercises that maintain balance during movement); the second group will receive static balance training (including exercises that hold a fixed posture); the third group will receive combined dynamic and static balance training (including both static and dynamic balance exercises); and the fourth group will serve as a control group without additional balance training (or receive regular physical education classes as a control).
The main outcomes to be measured before and after the training period are the participants' performance in specific stability tests, jumping tasks, and gymnastic movement skill assessments.
The goal is to determine which balance training method (dynamic, static, or combined training) is most effective in improving the fundamental movement skills (including gymnastics-specific abilities) of gymnastics beginners.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
-
Beijing, China
- Beijing Sport University
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Females
- Age ranged between 18 -22 years old, normal body mass index (BMI) (18.5 -25kg/m²).
- Undergraduate students of physical education at Beijing Sport University.
- No prior systematic gymnastics training (or with ≤ 1 year of systematic training experience), and no history of congenital diseases or musculoskeletal injuries.
Exclusion Criteria:
- Participants suffering from acute or chronic musculoskeletal injuries (lasting for 6 months or more), neurological disorders (such as epilepsy), or vestibular dysfunction.
- Ranked athletes or elite athletes.
- Participants with poor compliance (< 80%) who are unable to complete the 8 - week exercise intervention program.
- Individuals who have recently undergone or are scheduled to undergo surgery within three months.
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control group
|
An 8-week supervised training program conducted 2 times per week.
Each 15-30 minute session comprises a combination of static balance exercises , dynamic balance exercises and Combining training.
The intensity and difficulty of the exercises will be progressively increased throughout the intervention period.
|
|
Experimental: Static balance group
|
An 8-week supervised training program conducted 2 times per week.
Each 15-30 minute session comprises a combination of static balance exercises , dynamic balance exercises and Combining training.
The intensity and difficulty of the exercises will be progressively increased throughout the intervention period.
|
|
Experimental: Dynamic balance group
|
An 8-week supervised training program conducted 2 times per week.
Each 15-30 minute session comprises a combination of static balance exercises , dynamic balance exercises and Combining training.
The intensity and difficulty of the exercises will be progressively increased throughout the intervention period.
|
|
Experimental: Static and Dynamic balance group
|
An 8-week supervised training program conducted 2 times per week.
Each 15-30 minute session comprises a combination of static balance exercises , dynamic balance exercises and Combining training.
The intensity and difficulty of the exercises will be progressively increased throughout the intervention period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The 8-point Star Offset (cm)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Jump Height (cm)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Peak Force (N)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Rate of Force Development (N·S)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Impulse (N·s)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Center of gravity deviation distance (mm)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Joint Angle variation (°)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Vertical Jump Efficiency (%)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Landing Impact Force (N)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Body Oscillation Amplitude (mm)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Rotation Smoothness Index (°)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
Height (cm)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
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Weight (kg)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
|
BMI (kg/m2)
Time Frame: Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Baseline (pre-intervention) and at 8 weeks (immediately post-intervention)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
November 6, 2025
Primary Completion (Actual)
January 20, 2026
Study Completion (Actual)
January 20, 2026
Study Registration Dates
First Submitted
November 15, 2025
First Submitted That Met QC Criteria
December 3, 2025
First Posted (Actual)
December 17, 2025
Study Record Updates
Last Update Posted (Actual)
February 3, 2026
Last Update Submitted That Met QC Criteria
February 1, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- USM/JEPeM/KK/25070591
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
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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