- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05964556
Relationship Between the Functional Movement Screen and Isokinetic Muscle Strength of Knee in Different Sport Branches
July 27, 2023 updated by: TUĞBA BİRBEN, Recep Tayyip Erdogan University Training and Research Hospital
The Relationship Between The Functional Movement Screen and Isokinetic Muscle Strength of Knee in Different Sport Branches
This study was conducted to demonstrate the correlation between the functional movement screen and the isokinetic muscle strength with objective data.
Investigators conclude that the use of FMS in combination with isokinetic systems will provide more detailed information on the prevention of injuries to sports and the improvement of performance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was conducted to demonstrate the correlation between the functional movement screen and the isokinetic muscle strength with objective data.
60 athletes involved in volleyball, greco-roman, speed skating, athletics and taekwondo branches were included in the study.
The functional movement of the athletes was assessed by Functional Movement Screening, lower extremity isokinetic muscle strength was assessed by ISOMED 2000® isokinetic device.
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Guneysu
-
Rize, Guneysu, Turkey, 53390
- Recep Tayyıp Erdogan University Guneysu Vocational School of Physical Therapy and Rehabilitation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Carried out with 60 athletes between the ages of 12-30 who are interested in different or same sports branches.
Description
Inclusion Criteria:
- Those who voluntarily agreed to participate in the study
- Have at least 3 years of licensed sports experience
Exclusion Criteria:
- Those who have had or have ongoing orthopedic problems in the last 6 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Functional Movement Screen and Isokinetic Muscle Evulation of Knee Muscles
Functional movement screen was evaluated with 7 basic parameters determined by Gray Cook Isokinetic muscle measurements were performed with an ISOMED 2000
|
FMS is an analysis system that evaluates muscle strength imbalance and functional performances on the dominant-non-dominant side in athletes.
It aims to detect stability and mobility that can be ignored in the asymptomatic active population and athletes.
It consists of 7 basic parameters determined by Gray Cook (Deep Squat, Hurdle Step, -In-line Lunge, Shoulder Mobility, Active Straight Leg Raise, Trunk Stability, Rotatory Stability).
The athletes were evaluated after giving verbal instructions to the athletes about the head, trunk, knee and foot positions.
For each parameter, the athletes were given points between 0-3 values.
The total score was determined as 21 points.
Completing the movement completely and without compensation was given 3 points, and 2 or 1 points were given according to the activation of the compensation mechanism and balance disorders.
In case of any pain during or at the end of the movement in the evaluated parameter, 0 points were given to the athletes.
The isokinetic knee flexor and extensor group muscle strengths of the athletes participating in the study were measured on the dominant and non-dominant sides.
Measurements were performed with an ISOMED 2000 (D&R Ferstl GmbH, Hemau, Germany) isokinetic measuring device.
The test protocol was adjusted to be concentric/concentric.
Measurements were made at angular velocities of 60°/sec and 180°/sec.
At an angular speed of 60°/sec, the athlete was asked to perform 10 repetitions of voluntary knee flexion/extension at maximum strength.
Then, after resting for 30 seconds, 30 repetitions of knee flexion/extension were performed at an angular velocity of 180°/sec.
Before starting the test in both angular speeds, 3 repetitive attempts were made to learn the movement.
The following parameters were evaluated at 60°/sec and 180°/sec angular speed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Funtional Movement Screen (FMS)
Time Frame: 20 minutes
|
FMS is an analysis system that evaluates muscle strength imbalance and functional performances on the dominant-non-dominant side in athletes.
It aims to detect stability and mobility that can be ignored in the asymptomatic active population and athletes.
It consists of 7 basic parameters determined by Gray Cook (Deep Squat, Hurdle Step, -In-line Lunge, Shoulder Mobility, Active Straight Leg Raise, Trunk Stability, Rotatory Stability).
The athletes were evaluated after giving verbal instructions to the athletes about the head, trunk, knee and foot positions.
For each parameter, the athletes were given points between 0-3 values.
The total score was determined as 21 points.
Completing the movement completely and without compensation was given 3 points, and 2 or 1 points were given according to the activation of the compensation mechanism and balance disorders.
In case of any pain during or at the end of the movement in the evaluated parameter, 0 points were given to the athletes.
|
20 minutes
|
Isokinetic Measurement of Knee Muscles
Time Frame: 20 minutes
|
The isokinetic knee flexor and extensor group muscle strengths of the athletes participating in the study were measured on the dominant and non-dominant sides.
Measurements were performed with an ISOMED 2000 (D&R Ferstl GmbH, Hemau, Germany) isokinetic measuring device.
The test protocol was adjusted to be concentric/concentric.
Measurements were made at angular velocities of 60°/sec and 180°/sec.
At an angular speed of 60°/sec, the athlete was asked to perform 10 repetitions of voluntary knee flexion/extension at maximum strength.
Then, after resting for 30 seconds, 30 repetitions of knee flexion/extension were performed at an angular velocity of 180°/sec.
Before starting the test in both angular speeds, 3 repetitive attempts were made to learn the movement.
The following parameters were evaluated at 60°/sec and 180°/sec angular speed.
|
20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: TUGBA BIRBEN, PhD, Recep Tayyıp Erdogan University Guneysu Vocational School of Physical Therapy and Rehabilitation
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2017
Primary Completion (Actual)
August 1, 2017
Study Completion (Actual)
October 1, 2017
Study Registration Dates
First Submitted
July 16, 2023
First Submitted That Met QC Criteria
July 27, 2023
First Posted (Actual)
July 28, 2023
Study Record Updates
Last Update Posted (Actual)
July 28, 2023
Last Update Submitted That Met QC Criteria
July 27, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017/23
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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