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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02804685
Other study ID # DAG Research Group
Secondary ID
Status Completed
Phase N/A
First received June 8, 2016
Last updated October 25, 2016
Start date June 2016
Est. completion date October 2016

Study information

Verified date October 2016
Source University of Alcala
Contact n/a
Is FDA regulated No
Health authority Spain: Ministerio de Sanidad, Servicios Sociales e Igualdad
Study type Interventional

Clinical Trial Summary

This research presents a randomized clinical trial which evaluates the effectiveness of an exercise protocol on the knee-joint repositioning in futsal players related to a post-match muscle fatigue. Our hypothesis is the improvement of sensation in a knee in joint position before and after the match when performing our exercise program.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 16 Years to 24 Years
Eligibility Inclusion Criteria:

Must have three years of experience in futsal Must be Licensed players

Exclusion Criteria:

lower limb injuries

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention


Intervention

Other:
exercise protocol
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.

Locations

Country Name City State
Spain Guido Gómez Collado Villalba Madrid

Sponsors (1)

Lead Sponsor Collaborator
University of Alcala

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Joint Position Sense 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 Yes
Secondary Vertical jump heigh 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 Yes
Secondary Perceived exertion rate 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 Yes
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