- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03555175
Value Eccentric and Proprioception Exercise Into the Injury Effect in Amateur Football
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
There are three group with 10 participants each one. The group one will do hamstring eccentric exercise 12 series per 6 repeats. The group two will do three proprioception exercise 2 series per exercise and leg. And third group won't have add some exercise to their normal training.
All participants will do the exercises during 12 weeks. Before this 12 weeks they will be valuation with different tests, and this tests will have to repeat after this 12 weeks and 3 weeks after finish the exercises.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Daniela Fernández
- Phone Number: 610987248
- Email: daniela12fg@gmail.com
Study Locations
-
-
Madrid
-
Getafe, Madrid, Spain, 28905
- Recruiting
- Daniela Fernandez
-
Contact:
- Daniela Fernández
- Phone Number: 610987248
- Email: daniela12fg@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Training three times per week, add match day
- More than two years of experience
- Not be injured
- Not having been operated on the lower extremity
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Group one
This participants group must do eccentric exercise for 12 weeks
|
The group make hamstring eccentric exercise.
The participants have to do 12 serie of 6 repeats
|
Other: Group two
This participants group must do proprioception exercise for 12 weeks
|
The group have to do three kinds of exercise in a inestable area during 15 second in 2 repeats for each one
|
Other: Group 3
This participants group mustn't do exercise extra
|
Any exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Y-Test (star test)
Time Frame: Three time. Before intervention, at the end and three weeks post-intervention
|
Stability test.
The participants have to do three directions in the test antrior, posteromedial and posterolateral.
And they have to touch with their toe.
And the investigator will measure the distance between his support foot and his moving foot
|
Three time. Before intervention, at the end and three weeks post-intervention
|
Vertical Jump test
Time Frame: Three times. Before intervention, at the end and three weeks post-intervention
|
5 practice jumps with the hands in the hip, and we record this jumps.
The investigator will measure distance between the participants feet and the floor in the upper point
|
Three times. Before intervention, at the end and three weeks post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Weight
Time Frame: Before start
|
Scales [kilogram]
|
Before start
|
Years
Time Frame: Before start
|
Year of birth. Number
|
Before start
|
Height
Time Frame: Before start
|
Metre
|
Before start
|
Years playing football
Time Frame: Before start
|
Number of years. Number
|
Before start
|
Position in the team
Time Frame: Before start
|
name of position player. Name
|
Before start
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Daniela Fernandez, UAH
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- CEIM/HU/2018/06
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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