- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06331221
Effects of Different Concentric and Eccentric Muscle Fatigue Protocols on the Knee Joint Position Sense
Effects of Different Concentric and Eccentric Muscle Fatigue Protocols on the Knee Joint Position Sense: a Randomized Controlled Crossover Trial
Study Overview
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Joana Azevedo, MSc
- Phone Number: +351917910094
- Email: azevedojoana311@gmail.com
Study Locations
-
-
-
Porto, Portugal, 4200
- Recruiting
- Faculdade de Desporto, Universidade do Porto
-
Contact:
- Joana Azevedo, MSc
- Phone Number: +351917910094
- Email: azevedojoana311@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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