Effect of Instability Resistance Training on Balance, Core Muscle Strength, and Athletic Performance

May 21, 2024 updated by: Jianxin Gao, Universiti Putra Malaysia

Effect of Instability Resistance Training on Balance, Core Muscle Strength, and Athletic Performance Among Young Male Chinese Kayak Canoeists

The goal of this experimental study is to examine the effect of instability resistance training (IRT) on balance ability, core muscle strength, and athletic performance of young Chinese male kayak canoeists. The main questions it aims to answer are:

Do the IRT and TRT methods have any effect on the subject's balance ability in terms of static balance and dynamic balance? Do the IRT and TRT methods have any effect on the subject's isometric strength of the core muscle group in terms of abdomen, back, left lateral, and right lateral? Do the IRT and TRT methods have any effect on the subject's isotonic strength of the core muscle group in terms of flexion, extension, left lateral flexion, and right lateral flexion? Do the IRT and TRT methods have any effect on the subject's athletic performance in terms of dynamometer performance and calm-water performance?

Researchers will compare the effect of instability resistance training (IRT) and traditional resistance training (TRT) on balance ability, core muscle strength, and athletic performance of young Chinese male kayak canoeists.

Participants will:

Take 12-week instability resistance training (IRT) and traditional resistance training (TRT) difficulty level (primary level 1-4 weeks, intermediate level 5-8 weeks, and advanced-level 9-12 weeks).

Take 3 training sessions per week and complete the training on Mondays, Wednesdays, and Fridays from 4 to 5 pm.

Study Overview

Detailed Description

This study aimed to investigate the effect of a 12-week IRT on balance, core strength, and athletic performance among young male Chinese kayak canoeists. A Cluster Randomized Controlled Trial (CRCT) study was conducted. Firstly, the 2 city-level representative teams were chosen from 4 city-level representative teams of Jiangxi province and randomly assigned as two groups (experimental group and control group) using the Lottery Method. Secondly, 64 eligible kayak canoeists between the ages of 16-22 years (19.10±1.38) were recruited from the selected 2 city-level representative teams and randomly assigned to the instability resistance training (IRT) for the experimental group and traditional resistance training (TRT) for the control group using the same Lottery Method. The intervention was divided into 3 levels (primary, intermediate, and advanced) for IRT and TRT. Both groups performed training for 60 minutes, three times a week. The Swiss ball, BOSU ball, and Wobble boards were only provided with unstable surfaces for the IRT group. The intensity was body weight for both training methods. Dependent variables involving balance, core muscle strength, and athletic performance were measured using Flamingo Balance Test (FBT), Star Excursion Balance Test (SEBT), Abdomen Bridge (AB), Back Bridge (BB), Left and Right Lateral Bridge (LLB and RLB), 1min Sit-Up (SU), 1min Back Hyperextension (BH), 1min Left and Right Lateral V-up (LLV and RLV), K-1 200m Dynamometer Performance (DP), and Men's K-1 200m Calm-Water Performance (CWP) tests respectively in pre-test, post-test 1 (week 6), post-test 2 (week 12).

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

    • Selangor
      • Serdang, Selangor, Malaysia, 43400
        • Jianxin Gao

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
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Male, Aged 16-22, and Healthy

Exclusion Criteria:

Athletes who are systematically training their balance ability and core muscle strength

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Instability resistance training
After pre-testing, participants were randomly assigned to two groups. The participants of the IRT group were conducted in a 12-week (July 3 to September 22, 2023) Instability resistance training program that was performed one hour and three times per week (Mondays, Wednesdays, and Fridays from 4 to 5 pm) in the Nanchang Yao Lake base.
The 20 intervention actions were divided into three levels (primary, intermediate, and advanced) for instability resistance training and traditional resistance training. Both groups performed training for 60 minutes three times a week. The Swiss ball, BOSU ball, and Wobble boards only provided an unstable surface environment for instability resistance training. The intensity/load was body weight for both training methods.
Experimental: Traditional resistance training
After pre-testing, participants were randomly assigned to two groups. The participants of the TRT group were conducted in a 12-week (July 3 to September 22, 2023) traditional resistance training program that was performed one hour and three times per week (Mondays, Wednesdays, and Fridays from 4 to 5 pm) in the Ganzhou Shangyou base.
The 20 intervention actions were divided into three levels (primary, intermediate, and advanced) for instability resistance training and traditional resistance training. Both groups performed training for 60 minutes three times a week. The Swiss ball, BOSU ball, and Wobble boards only provided an unstable surface environment for instability resistance training. The intensity/load was body weight for both training methods.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Static Balance
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Flamingo Balance Test
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Dynamic Balance
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Star Excursion Balance Test
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Abdomen Core Strength
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Abdomen Bridge
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Back Core Strength
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Back Bridge
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Left Lateral Core Strength
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Left Lateral Bridge
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Right Lateral Core Strength
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Right Lateral Bridge
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Dynamometer Performance
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Men's K-1 200m Dynamometer Performance
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Calm-Water Performance
Time Frame: This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)
Men's K-1 200m Calm-Water Performance
This study collected data in pre-test (before intervention), post-test 1 (6 weeks after intervention), and post-test 2 (12 weeks after intervention)

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)

June 19, 2023

Primary Completion (Actual)

September 22, 2023

Study Completion (Actual)

September 22, 2023

Study Registration Dates

First Submitted

January 7, 2024

First Submitted That Met QC Criteria

May 21, 2024

First Posted (Actual)

May 29, 2024

Study Record Updates

Last Update Posted (Actual)

May 29, 2024

Last Update Submitted That Met QC Criteria

May 21, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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