Effects of Eccentric Potentiation Activation on Muscle Function

April 19, 2024 updated by: Brennan Thompson

Effects of Multi-joint Eccentric Potentiation Maximal Contractions on Muscle Function

The purpose of this study is to examine the potentiation effects of 2 sets of multi-joint eccentric overload maximal contractions on muscle function.

Study Overview

Status

Withdrawn

Study Type

Interventional

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 Contact

Study Contact Backup

Study Locations

    • Utah
      • Logan, Utah, United States, 84322
        • Utah State 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

16 years to 28 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Exclusion Criteria:

  • lower body surgery or injury in the last 12 months
  • have any neuromuscular disease
  • height >76 inches tall
  • height <54 inches tall
  • eccentric strength greater than 725 pounds
  • pregnant or plan to be pregnant in the duration of the protocol
  • don't do resistance exercise at least once per week
  • perform intense cardio or strength training >4 days per week
  • Present with any other significant comorbid conditions that would impair the ability to participate in the exercise-based testing

Inclusion criteria:

  • 18 - 30 years old
  • strength train lower body 1-3 times per week

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: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Cycling exercise
Cycling on a cycle ergometer instead of doing the experimental eccentric exercise.
Individuals will do a randomized crossover intervention involving cycling (active control) exercise
Experimental: Eccentric exercise
Perform 2 sets of maximal eccentric contractions as the single session exercise intervention.
Individuals will do a randomized crossover intervention involving maximal eccentric contractions (2 sets of 6 per leg; experimental condition)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump
Time Frame: Baseline (pretest)
3 countermovement vertical jumps, with 30 seconds of rest between attempts
Baseline (pretest)
Vertical Jump
Time Frame: Immediately post intervention
3 countermovement vertical jumps, with 30 seconds of rest between attempts
Immediately post intervention
Vertical Jump
Time Frame: 12 minutes post intervention
3 countermovement vertical jumps, with 30 seconds of rest between attempts
12 minutes post intervention
Vertical Jump
Time Frame: 20 minutes post intervention
3 countermovement vertical jumps, with 30 seconds of rest between attempts
20 minutes post intervention
Isokinetic eccentric maximal strength
Time Frame: Baseline (pretest)
Maximal eccentric strength on the Eccentron machine. 2 repetitions per time point
Baseline (pretest)
Isokinetic eccentric maximal strength
Time Frame: Immediately post intervention
Maximal eccentric strength on the Eccentron machine. 2 repetitions per time point
Immediately post intervention
Isokinetic eccentric maximal strength
Time Frame: 12 minutes post intervention
Maximal eccentric strength on the Eccentron machine. 2 repetitions per time point
12 minutes post intervention
Isokinetic eccentric maximal strength
Time Frame: 20 minutes post intervention
Maximal eccentric strength on the Eccentron machine. 2 repetitions per time point
20 minutes post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Brennan J Thompson, PhD, Utah State University

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 1, 2022

Primary Completion (Actual)

March 1, 2024

Study Completion (Actual)

March 1, 2024

Study Registration Dates

First Submitted

October 24, 2022

First Submitted That Met QC Criteria

October 28, 2022

First Posted (Actual)

November 4, 2022

Study Record Updates

Last Update Posted (Actual)

April 23, 2024

Last Update Submitted That Met QC Criteria

April 19, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 12042c

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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