Effects of Different Concentric and Eccentric Muscle Fatigue Protocols on the Knee Joint Position Sense

March 19, 2024 updated by: Universidade do Porto

Effects of Different Concentric and Eccentric Muscle Fatigue Protocols on the Knee Joint Position Sense: a Randomized Controlled Crossover Trial

The aim of this study was to investigate the effects of different concentric and eccentric muscle fatigue protocols on the knee joint position sense of healthy individuals.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

A randomized controlled crossover trial will be conducted at a biomechanics laboratory with healthy males. All participants will perform with a washout period of 1 week: a control condition (5-minute rest) and 4 local muscle fatigue protocols (concentric of quadriceps; concentric of hamstrings; eccentric of quadriceps; eccentric of hamstrings) in an isokinetic dynamometer at 30º/s. Three maximum voluntary isometric contractions (MVIC) of quadriceps and hamstrings will also be assessed in the beginning of all conditions.

Knee joint position sense will be assessed before and immediately after the fatigue protocols/control condition, through active concentric and eccentric positionings/repositionings, in sitting and prone positions, to a target range of 45º of knee flexion in an isokinetic dynamometer. Surface electromyography electrodes will also be placed on the vastus lateralis and biceps femoris during all procedures.

Study Type

Interventional

Enrollment (Estimated)

20

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 Locations

      • Porto, Portugal, 4200
        • Recruiting
        • Faculdade de Desporto, Universidade do Porto
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • males aged between 18 and 30 years;
  • without current or previous knee pathology or surgery;
  • with a low or moderate physical activity level, according to the International Physical Activity Questionnaire;
  • normal Body Mass Index (under 24.9 kg/m2), according to the World Health Organization.

Exclusion Criteria:

  • those with cardiorespiratory, neurological or vestibular pathologies;
  • with positive knee integrity tests (anterior drawer, Lachman's test, posterior drawer; valgus and varus stress testes); and
  • those taking any medication that can affect motor control (sedatives, anxiolytics, antibiotics, analgesics, NSAIDs or myorelaxants).

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Condition
5-minute rest period.
Active Comparator: Quadriceps_Concentric
40 consecutive maximal concentric contractions of quadriceps at 30º/s from the 90° to 30° of knee flexion
Four experimental conditions consisting of different local muscle fatigue protocols performed in the isokinetic dynamometer in random order, with at least one week of interval between them.
Active Comparator: Quadriceps_Eccentric
40 consecutive maximal eccentric contractions of quadriceps at 30°/s from the 30° to 90° of knee flexion
Four experimental conditions consisting of different local muscle fatigue protocols performed in the isokinetic dynamometer in random order, with at least one week of interval between them.
Active Comparator: Hamstrings_Concentric
30 consecutive maximal concentric contractions of hamstrings at 30º/s from 30º to 90º of knee flexion
Four experimental conditions consisting of different local muscle fatigue protocols performed in the isokinetic dynamometer in random order, with at least one week of interval between them.
Active Comparator: Hamstrings_Eccentric
30 consecutive maximal eccentric contractions of the hamstrings at 30º/s from 90º to 30º of knee flexion
Four experimental conditions consisting of different local muscle fatigue protocols performed in the isokinetic dynamometer in random order, with at least one week of interval between them.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Absolute angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The absolute value of the difference between the target range and the achieved range
Change from Baseline (Before) to Immediately after interventions or control (After)
Relative angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The arithmetic difference between the target range and the range achieved
Change from Baseline (Before) to Immediately after interventions or control (After)
Variable angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The standard deviation of the 3 repositionings
Change from Baseline (Before) to Immediately after interventions or control (After)

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)

November 2, 2023

Primary Completion (Estimated)

May 15, 2024

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

March 19, 2024

First Submitted That Met QC Criteria

March 19, 2024

First Posted (Actual)

March 26, 2024

Study Record Updates

Last Update Posted (Actual)

March 26, 2024

Last Update Submitted That Met QC Criteria

March 19, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • JSA_Fatigue_FADEUP

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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