- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06162130
Muscular Activations During Eccentric Quadriceps Exercises
Investigation of Muscular Activations During Eccentric Quadriceps Exercises
Study Overview
Status
Intervention / Treatment
Detailed Description
The quadriceps muscle is known to be crucial for the dynamic control of the lower extremity, and weakness in this muscle can lead to strategies that may result in injury. Therefore, acquiring optimal quadriceps muscle strength is essential not only for preventing lower extremity injuries but also for enabling individuals to fully return to activities after an injury.
Despite the existence of various eccentric quadriceps exercises in the literature, there is a lack of consensus on their comparative effectiveness. Hence, there is a requirement for research to explore the effectiveness of different eccentric quadriceps exercises. The objective of this study is to compare the muscular activation of the quadriceps muscle during four distinct eccentric quadriceps exercises using surface electromyography (sEMG) devices
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Ankara, Turkey
- Gazi University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Being a licensed athlete in one's own field, Having been engaged in sports for at least 2 years
Exclusion Criteria:
Individuals with any musculoskeletal injury history in the lower extremities and trunk that could impede exercise within the last year, Individuals with systemic, neurological, and/or cognitive issues, Individuals experiencing pain in the lower extremities and trunk during exercises
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Other
female athletes
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The activation of the vastus medialis, vastus lateralis, and rectus femoris muscles will be measured using surface electromyography (sEMG) during four distinct quadriceps eccentric exercises: Reverse Nordic, Pistol squat, Suspension-based Bulgarian split squat, and Bulgarian split squat.
Participants will be instructed to perform three successful repetitions for each exercise.
A 30-second break will be provided between each repetition, and there will be a minimum of 10 minutes of rest between each of the four exercises.
Due to the belief that fatigue could impact exercise performance, the modified Borg scale will be used to ensure that fatigue does not occur before each exercise.
Exercise recording will commence when scores reported using the modified Borg scale are 1 or lower.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Surface EMG Measurement
Time Frame: in an average of one hour
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During data collection, the EMG Noraxon MiniDTS system (Noraxon Inc.) was used to measure the signals from the muscle.
Additionally, the participants were video-recorded to prevent any potential mistakes that might have gone unnoticed during the activities.
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in an average of one hour
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Normalization of Surface EMG
Time Frame: in an average of one hour
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To normalize the EMG data obtained during the exercises, MVIC will be performed for each muscle using an isokinetic dynamometer.
Participants will be shown a video demonstrating the movement for MVIC, and before the test, they will be asked to warm up for 5 minutes on a treadmill at submaximal speed and then perform the movement.
To ensure electromyography (EMG) normalization, participants will be asked to perform 3 repetitions, and the average of these three values will be taken.
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in an average of one hour
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Elif AYGUN POLAT, PhD, T.C. ORDU ÜNİVERSİTESİ
- Study Director: Nevin A. GUZEL, Prof, Gazi University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- ODUSBFFTR-ELIFAYGUNPOLAT-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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