- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04204460
Electromyographic Evaluation of Quadriceps During Eccentric Decline Squat
Electromyographic Evaluation of Quadriceps During Eccentric Decline Squat: An Investigation of the Effect of Decline Angle and Arc of Motion
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Sevim Acaröz Candan, PhD
- Phone Number: 6536 004522265200
- Email: fzt_acaroz@hotmail.com
Study Locations
-
-
Altinordu
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Ordu, Altinordu, Turkey, 52100
- Sevim ACARÖZ CANDAN
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- had exercised regularly (>3 days in a week) for at least six months.
- older than 18 years old.
Exclusion Criteria:
- had patellofemoral pain, knee pain otherwise unrelated to the knee extensor mechanism and other injuries that would restrict performance of the tasks (e.g. ankle pathology).
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Crossover
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Electromyographic measurement of muscle activation
Time Frame: 50 minutes
|
Surface electromyographic (EMG) system (Noraxon Telemyo DTS System, Scottsdale, USA) will be use to measure the muscle activation ratios of RF, VL, and VMO. Electrodes will be placed according to Surface EMG for noninvasive assessment of muscles (SENIAM) recommendations on the dominant leg. The muscle activation during eccentric phase of the decline squat for RF, VL, and VMO will be determined. The decline squat will be performed under different conditions (various decline angle: 0, 5, 10,15, 20 degree) The muscle activation will also be investigated within various arc of motion of knee flexion (0-30, 30-60, 60-90, 0-60, 0-90, 30-90) which is determined using the motion analysis system (Noraxon, MYOmotion Scottsdale, USA). |
50 minutes
|
Maximal voluntary isometric contractions (MVICs)
Time Frame: 5 minutes
|
MVICs for the RF, VL, and VMO at their manual muscle test positions will be assessed within 3 trials, which lasts 5 seconds.
The muscle test position will be standardized 90 degrees hip flexion and 60 degrees knee flexion.
One minute a rest period will be between each trial.
The peak EMG amplitude will be used for the normalization.
|
5 minutes
|
Normalized EMG values
Time Frame: 5 minutes
|
The amount of muscle activation in each condition will be proportioned to MVICs value for normalization using a calculator.
The value will be represented in percentile (%).
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Weight
Time Frame: 1 minute
|
The participant's weight will be determined a weighing machine inkilogram.
|
1 minute
|
Height
Time Frame: 1 minute
|
The participant's height will be measured in cm.
|
1 minute
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sevim ACARÖZ CANDAN, PhD, T.C. ORDU ÜNİVERSİTESİ
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- OrduU6
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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