Resistance Exercise Training in Children.

October 10, 2023 updated by: Trent J. Herda, Ph.D., University of Kansas Medical Center

The Effects of Resistance Exercise on Muscle Activation and Lipids in Children

The purpose of this study is examine the effects of 8 weeks (3 days/week) of resistance exercise training in children 8 to 10 years of age on muscle strength, activation, and lipids of the vastus lateralis.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

32

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

    • Kansas
      • Kansas City, Kansas, United States, 66103
        • Hoglund Biomedical Imaging Center
      • Overland Park, Kansas, United States, 66213
        • Exercise and Human Performance Laboratory
      • Overland Park, Kansas, United States, 66213
        • Metabolic and Body Composition Laboratory
    • Missouri
      • Kansas City, Missouri, United States, 64108
        • Energy Balance Laboratory

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

Yes

Description

Inclusion Criteria:

  • Healthy volunteer males and females ages 8 - 10 years.

Exclusion Criteria:

  • No history or ongoing neuromuscular diseases, musculoskeletal injuries, or a disease that effects metabolism.

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: Basic Science
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Resistance exercise training
Participants undergo 8 weeks (3 days/week) of resistance exercise training.
Traditional linear periodization resistance training.
No Intervention: Control
Participants do not perform 8 weeks of resistance exercise training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the muscular strength of leg extensors, as measured with isometric strength.
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect the strength of the leg extensors. The higher score, reflects greater muscular strength.
baseline, following the intervention (9 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in motor unit firing rates during a 60% of maximal voluntary contraction (MVC).
Time Frame: baseline, following the intervention (9 weeks)
Scores are measured with the y-intercept from the firing rates versus recruitment threshold relationships from the 60%. The higher y-intercept score reflects greater muscle activation.
baseline, following the intervention (9 weeks)
Change from baseline in motor unit firing rates during a 60% of maximal voluntary contraction (MVC).
Time Frame: baseline, following the intervention (9 weeks)
Scores are measured with the slope from the firing rates versus recruitment threshold relationships from the 60%. The higher slope score reflects greater muscle activation.
baseline, following the intervention (9 weeks)
Change from baseline in thigh muscle cross-sectional area.
Time Frame: baseline, following the intervention (9 weeks)
Scores are measured cross-sectional area from ultrasound images.
baseline, following the intervention (9 weeks)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in the fatty acid saturation levels of the extramyocellular lipids of the vastus lateralis, as measure with magnetic resonance spectroscopy
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect a saturation level of fatty acids in the extramyocellular lipid. The higher score, reflects greater fatty acid saturation.
baseline, following the intervention (9 weeks)
Change from baseline in the fatty acid saturation levels of the intramyocellular lipids of the vastus lateralis, as measure with magnetic resonance spectroscopy
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect a saturation level of fatty acids in the intramyocellular lipid. The higher score, reflects greater fatty acid saturation.
baseline, following the intervention (9 weeks)
Change from baseline in motor unit firing rates during a 35% of maximal voluntary contraction (MVC).
Time Frame: baseline, following the intervention (9 weeks)
Scores are measured with the y-intercepts from the firing rates versus recruitment threshold relationships from the 35%. The higher y-intercept score reflects greater muscle activation.
baseline, following the intervention (9 weeks)
Change from baseline in motor unit firing rates during a 35% of maximal voluntary contraction (MVC).
Time Frame: baseline, following the intervention (9 weeks)
Scores are measured with the slopes from the firing rates versus recruitment threshold relationships from the 35%. The higher slope score reflects greater muscle activation.
baseline, following the intervention (9 weeks)
Change from baseline in intramyocellular lipids of the vastus lateralis, as measure with magnetic resonance spectroscopy
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect a concentration. The higher score, reflects more fat in the fibers.
baseline, following the intervention (9 weeks)
Change from baseline in extramyocellular lipids of the vastus lateralis, as measure with magnetic resonance spectroscopy
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect a concentration. The higher score, reflects more fat in the fibers.
baseline, following the intervention (9 weeks)

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)

August 2, 2021

Primary Completion (Actual)

September 6, 2023

Study Completion (Actual)

September 6, 2023

Study Registration Dates

First Submitted

October 5, 2023

First Submitted That Met QC Criteria

October 10, 2023

First Posted (Actual)

October 11, 2023

Study Record Updates

Last Update Posted (Actual)

October 13, 2023

Last Update Submitted That Met QC Criteria

October 10, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • ICF

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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