- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02804685
Effectiveness of an Exercise Protocol on Alteration of Knee Joint Position Sense in Futsal Players
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Madrid
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Collado Villalba, Madrid, Spain, 28400
- Guido Gómez
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Must have three years of experience in futsal Must be Licensed players
Exclusion Criteria:
lower limb injuries
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
It consists on only a regular training performance
|
|
Experimental: Experimental
It consists on performing the protocol which includes 6 strength, agility and balance exercises together with the regular training.
The exercise program has to be performed twice a week during 6 weeks
|
The multi-intervention exercise protocol consists in a performance of agility, strength and balance exercises.
It has to be fulfilled during 6 weeks (twice a week) before the regular training performance.
The exercises should be done for almost 15 minutes approx.
There will be 6 exercises in total: squat with toe raise, one-leg squats, single-leg balance (throwing a ball with a partner), vertical jumps, hamstring exercise, quick forwards and backwards sprints.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Joint Position Sense
Time Frame: up to 6 weeks after the end of the intervention
|
Joint Position Sense: Pictures of the knee joint repositioning of the participant are taken.
The camera is placed perpendicularly 2 m from the knee joint and 65 cm from the ground.
As references, 4 markers are placed in the lower extremity.
The participant is seated with his feet dangling and his eyes closed.
The dominant leg of the participant is passively carried by the examiner to 45 ° knee flexion.
The participant is asked to maintain that position for 10 seconds.
After that examiner returns the leg of the player to initial position in a passive way.
The participant is then asked to change the position of the leg in an active way to the target position and maintain it for 4 seconds.
After that he should return to the initial position.
This exercise should be done 3 times.
In each position a photograph is taken and then all of them are measured by Autocad which specifies the angles.
The absolute angular error, the relative angular error and the variable angular error are measured.
|
up to 6 weeks after the end of the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Vertical jump heigh
Time Frame: up to 6 weeks after the end of the intervention
|
Vertical jump height: for this, computer software "HSC-Kinovea" must be used. To perform the jump, hands should be placed on hips and the maximum impulse should be taken with both legs in order to take off from the ground. Each participant performs 5 preparatory jumps and then another 5 jumps (as high as possible). These 5 last jumps are the ones that will be analyzed. The height of the best jump is obtained through the formula mentioned above. The flight time of these 5 jumps will be recorded with a camera that films 240 frames per second (Canon PowerShot SX700 HS). The analysis of the data is done with the software "Kinovea 0.8.15 for Windows" that measures the time difference between the first frame in which both feet are taking off the floor and the frame in which only one or both feet land. This measurement allows us to relate the height of each jump with muscle fatigue |
up to 6 weeks after the end of the intervention
|
Perceived exertion rate
Time Frame: up to 6 weeks after the end of the intervention
|
Perceived exertion rate is obtained through the Borg Scale for Perceived Exertion (Borg's 6 to 10 Rating of Perceived Exertion Scale) with the aim of relating the subjective perception of the effort with objective measures of muscle fatigue. It is a discrete quantitative variable. Borg Scale for Perceived Exertion will be given to the participants at the end of each match. It consists of a list of numbers from 6 to 20 which are related to subjective expressions of effort (no effort: 6, extremely light: 7-8, very light: 9, light 11 moderate: 13, hard 15, very hard 17, extremely hard: 19, maximum effort: 20). The participant will be asked how they felt during this physical activity (in relation with the effort). The collected data will be related to the numeric value. |
up to 6 weeks after the end of the intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DAG Research Group
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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