Effects of Unstable Core Training on Sport Performance Among Kayakers

NCT07742267 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-08-03

No results posted yet for this study

Summary

A randomized controlled trial was conducted, recruiting 24 eligible kayakers aged 14-22 years from the Jiangxi training base, China. Participants were randomly assigned to the SUCT group and the DUCT group. Both groups completed a 12-week unstable core training program consisting of 1-hour sessions, 3 times/week. Balance ability was assessed using the flamingo balance test and star excursion balance test. Trunk muscle strength was assessed using the abdomen, back, side bridge tests, sit-up, back extension, and trunk rotation tests. Paddling performance was evaluated using the average stroke power and stroke rate for the men's K-1 200m land ergometer sprint tests.

Conditions

  • Athletic Performance
  • Resistance Training
  • Kayaking

Interventions

BEHAVIORAL

static unstable core training (SUCT) for the experimental group

The SUCT group performed static exercises (Plank on BOSU ball, Shoulder Bridge on Swiss ball, Side Plank on wobble boards, Dead Bug on BOSU ball, Static Superman on BOSU ball).

BEHAVIORAL

dynamic unstable core training (DUCT) for the control group

The DUCT group performed dynamic exercises (Crunch on Swiss ball, Supine Hip Up on BOSU ball, Palfo Press on wobble boards, Dynamic Superman on BOSU ball, Russian Twist on BOSU ball).

Sponsors & Collaborators

  • Gao Jianxin

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
22 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-01
Primary Completion
2023-09-30
Completion
2023-09-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07742267 on ClinicalTrials.gov