- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04885725
Association Between Knee Isokinetic Testing and Lower Limb Functional Performance and Limb Symmetry (Pro-knee)
This study aimed to evaluate the association between the isokinetic knee strength and/or proprioception performance with the functional performance on the functional Hop-tests and Y-balance test.
This study included 20 healthy individuals who performed an isokinetic assessment of knee proprioception (joint position sense, JPS and threshold to detection of passive motion, TDPM) and flexors/extensors strength. At the same time, they performed a functional testing consisting of three Hop-tests (single, triple and cross-over) and the Lower Quarter Y-Balance Test (YBT-LQ). We tested the correlation between the isokinetic and functional performances, and limb symmetry indexes.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Caen, France, 14000
- CHU Caen Normandie
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- individuals under 45 years of age who performed at least 4 hours of physical activity per week.
Exclusion Criteria:
- individuals unable to perform isokinetic muscle tests
- individuals with a current or recent lower limb injury with time loss from sport participation within the previous month
- individuals with previous severe knee injury (eg. Severe ligament tear, knee fracture)
- individuals taking medications with potential balance/coordination side effects.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Strength
Time Frame: one evaluation at a single point in time through study completion, an average of 4 months
|
Measurement of knee extensors and flexors peak strength (in newton.meter,
Nm) on isokinetic dynamometer.
|
one evaluation at a single point in time through study completion, an average of 4 months
|
|
Knee proprioception, JPS1
Time Frame: one evaluation at a single point in time through study completion, an average of 4 months
|
Measurement of knee proprioception by the passive repositioning technique (JPS, in degrees) on isokinetic dynamometer.
|
one evaluation at a single point in time through study completion, an average of 4 months
|
|
Knee proprioception, JPS2
Time Frame: one evaluation at a single point in time through study completion, an average of 4 months
|
Measurement of knee proprioception by the active repositioning technique (JPS, in degrees) on isokinetic dynamometer.
|
one evaluation at a single point in time through study completion, an average of 4 months
|
|
Knee proprioception, TDPM
Time Frame: one evaluation at a single point in time through study completion, an average of 4 months
|
Measurement of knee proprioception by the Threshold to Detection of Passive Motion (TDPM in degrees) on isokinetic dynamometer.
|
one evaluation at a single point in time through study completion, an average of 4 months
|
|
Functional testing, Hop tests
Time Frame: one evaluation at a single point in time through study completion, an average of 4 months
|
Hop test. Single hop: Patients are instructed to stand on one leg and perform 1 jump as far as possible, landing on the same leg. The total distance is recorded (in cm) .Triple hop: Patients are instructed to stand on one leg and perform 3 hops as far as possible, landing on the same leg. The total distance for 3 consecutive hops is recorded (in cm). Cross-over hop test : The patient hops forward 3 times while alternately crossing over a marking The patient is instructed to position themselves such that the first of the 3 hops was lateral with respect to the direction of crossover The total distance hopped forward is recorded (in cm) |
one evaluation at a single point in time through study completion, an average of 4 months
|
Collaborators and Investigators
Sponsor
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
- Pro-knee
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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