The Importance of Exercise to Prevent Injuries in Athletes
EFFECTIVENESS OF A PROPRIOCEPTIVE EXERCISE PROGRAM IN THE PREVENTION OF INJURIES IN RECREATIONAL RUNNERS
Introduction: running is one of the most accessible and practiced sports in the world since the 21st century. Unfortunately, the incidence of injuries in the population that practices it is high regardless of experience, although the risk of injury increases in amateur runners. One of the main keys to reduce the incidence of running related injuries may be to improve the ability to reduce the load or impact. For this, there are different strategies such as a gradual increase in the load to run, and exercise within which is muscle strengthening and balance training or proprioception.
Objective: to verify the effectiveness of a program of proprioceptive exercises based on the static and dynamic balance for the reduction of lower limb injuries in amateur runners during the competition season.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Methodology: 66 amateur runners, after simple size calculation, will be randomized into two groups. Experimental group will carry out the proprioceptive exercise program during 8 weeks at the begining of the season and control group will continue with their usual training routine. The main variable running related injury will be collected weekly during the follow-up.
Results: When all the data needed for the study has been collected, researchers gathers results and exports them for statistical interpretation.
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Madrid
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Alcala de Henares, Madrid, Spanje, 28871
- Grupo Fisioterapia y Dolor
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Weekly training of at least 15 kilometers.
- At least practice running 6 months for 1-3 times a week.
Exclusion Criteria:
- To have some type of lower limb or lower back injury at present or in the last 6 months.
- Having undergone surgery for any back or lower limb injury.
- Pregnant.
- Neural dysfunction / disability.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Experimental group
Group will carry out the proprioceptive exercise program during 8 weeks at the begining of the season
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Group A will carry out two sessions of proprioceptive training per week, in a total of 8 weeks, during the pre-season period (September-October).
Each session will last approximately 30 minutes and will include 6 exercises.
The execution of the exercises will be supervised by a physiotherapist and a national trainer of athletics.
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Placebo-vergelijker: Control group
Control group will continue with their usual training routine
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The subjects of the control group (group B) will be informed so that they do not include any change in their usual training routine.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Knee Joint Position Sense (JPS)
Tijdsspanne: Change from Baseline Joint Position Sense Pressure at 8 weeks
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JPSThe JPS is defined as the awareness of the actual position of the limb to quantify proprioception.The method for measuring JPS is to place the joint at a specific target angle and then, after the limb has been moved back to the starting angle, the subject is asked to actively or passively reproduce the target angle.
The outcome of the measurement is the absolute error (AE), which is the difference between the true target angle and the reproduced angle
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Change from Baseline Joint Position Sense Pressure at 8 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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The Y Balance Test (YBT)
Tijdsspanne: Change from Baseline dynamic balance at 8 weeks
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The YBT, derived from the Star Excursion Balance Test (SEBT), has been reported to be a valid and reliable measure of dynamic balance; furthermore, the results of the YBT have been reported to be related to lower-extremity impairments and to be predictors of injuries.The YBT instrument has a central raised platform with three pieces of PVC (polyvinyl chloride) pipe in the three directions with a sliding plastic reach indicator that the participant pushes to determine reach distance.The YBT testing protocol assessed absolute reach and normalized distance for each direction, asymmetry between limbs, and composite score.
Normalized reach distance is calculated by dividing reach distance by the limb length.
Asymmetry is the absolute difference between right and left leg and is determined for each reach direction.
The composite score is calculated by summing the reach distance in the three directions, dividing by three times limb length, and multiplying by 100.
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Change from Baseline dynamic balance at 8 weeks
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The countermovement jump (CMJ)
Tijdsspanne: Change from Baseline jump height at 8 weeks
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The CMJ is primarily used to measure an athlete's explosive lower-body power, and has become one of the most frequently used tests by coaches and researchers to indirectly measure power in the lower limbs.
CMJ performance is reported as either jump height(centimeters).
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Change from Baseline jump height at 8 weeks
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie stoel: Tomas Gallego-Izquierdo, Dr., Alcalá University
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- CEIM/HU/2018/29
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
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