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

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:

  1. Females
  2. Age ranged between 18 -22 years old, normal body mass index (BMI) (18.5 -25kg/m²).
  3. Undergraduate students of physical education at Beijing Sport University.
  4. No prior systematic gymnastics training (or with ≤ 1 year of systematic training experience), and no history of congenital diseases or musculoskeletal injuries.

Exclusion Criteria:

  1. Participants suffering from acute or chronic musculoskeletal injuries (lasting for 6 months or more), neurological disorders (such as epilepsy), or vestibular dysfunction.
  2. Ranked athletes or elite athletes.
  3. Participants with poor compliance (< 80%) who are unable to complete the 8 - week exercise intervention program.
  4. 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)
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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