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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04885725
Other study ID # Pro-knee
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 5, 2019
Est. completion date September 26, 2020

Study information

Verified date May 2021
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date September 26, 2020
Est. primary completion date March 15, 2020
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Device:
All group
All the participants performed the isokinetic proprioception and strength tests and the functional tests, on the same visit.

Locations

Country Name City State
France CHU Caen Normandie Caen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Strength 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
Primary Knee proprioception, JPS1 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
Primary Knee proprioception, JPS2 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
Primary Knee proprioception, TDPM 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
Primary Functional testing, Hop tests 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
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