Strength Training and Muscle Lipids (Strength-Lip)

August 14, 2025 updated by: University of Kansas Medical Center

The Effects of Strength Training on Neuromuscular Function and Muscle Lipids.

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 and power, motor unit activation, and lipid profiles of the vastus lateralis.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

14

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
      • Lawrence, Kansas, United States, 66045
        • Neuromechanics Laboratory
      • Overland Park, Kansas, United States, 66213
        • Exercise and Human Performance Laboratory
      • Overland Park, Kansas, United States, 66213
        • Metabolic and Body Composition 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.
  • No history or ongoing musculoskeletal injuries.
  • No history or ongoing 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
No Intervention: Control
Experimental: Resistance exercise training
Participants will strength train via linear periodization resistance exercise training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in muscular power of the leg extensors, as measured with isokinetic strength testing.
Time Frame: Baseline, following the intervention (9 weeks)
The score will reflect the muscular power 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 thigh muscle cross-sectional area
Time Frame: Baseline, following the intervention (9 weeks)
Scores are measured cross-sectional area from ultrasound images. The higher score, reflects greater muscle size of the leg extensors.
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 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)
Change from baseline in motor unit activation, as measured with surface electromyography decomposition.
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect the firing rates of recorded motor units. The higher score, reflects greater motor unit activation.
baseline, following the intervention (9 weeks)
Change in total body lean mass, as measured with bioelectrical impedance analysis.
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect the lean mass. The higher score, reflects greater lean mass.
baseline, following the intervention (9 weeks)
Change in total body fat mass, as measured with bioelectrical impedance analysis.
Time Frame: baseline, following the intervention (9 weeks)
The score will reflect the fat mass. The higher score, reflects greater fat mass.
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)

July 1, 2024

Primary Completion (Actual)

December 7, 2024

Study Completion (Actual)

December 7, 2024

Study Registration Dates

First Submitted

June 24, 2024

First Submitted That Met QC Criteria

June 24, 2024

First Posted (Actual)

June 28, 2024

Study Record Updates

Last Update Posted (Actual)

August 20, 2025

Last Update Submitted That Met QC Criteria

August 14, 2025

Last Verified

August 1, 2025

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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