- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02927418
Strength Training for Injury Prevention
5 de mayo de 2017 actualizado por: University of Manitoba
The purpose of this study is to explore the effects of a strength & conditioning (S & C) program on risk factors for injury (Y-balance and Functional Movement Screen scores), as well as parent reported injury occurrence in 12-16 year old male and female athletes.
Forty girls and 40 boys aged 12-16 will be recruited; half will participate in supervised S & C sessions 2-3x/week while the other half will continue with their regular sports and activities.
Risk factors for injury and performance indices (20 m sprint and multiple jump test) will be assessed before and after the 4 month study.
Injury occurrence will be recorded via bi-weekly phone calls to the parent and athlete.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
43
Fase
- No aplica
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
12 años a 16 años (Niño)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Athletes between 12 and 16 years of age, actively participating in organized sport
Exclusion Criteria:
- Any condition or injury that will place the athlete at risk during testing or training
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Strength & Conditioning
Supervised S & C program based on the Long Term Athlete Development Model.
Participants will attend 2-3 sessions per week for about one hour each session for 4 months.
The comprehensive program will include strength and power training as well as plyometrics, agility and flexibility exercises.
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Comparador activo: Control
Athletes in the control group will continue with their usual sports and activities but will not receive any type of training.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Y-balance score
Periodo de tiempo: 4 months
|
Using the Y Balance Test Kit (Functional Movement Systems, Inc., Chatham, Virginia), the athlete stands on one leg, hands on hips, while pushing a wooden block as far forward as possible with the opposite foot.
The displacement of the block is recorded.
The athlete is allowed 4 practice trials in each of the 3 test directions: anterior, posteromedial and posterolateral.
Three test trials are then conducted for each leg in each direction, with short rest breaks between trials.
The average reach distance for each leg for each direction will be normalized to leg length and used in analyses.
This test has shown moderate to excellent reliability.
Lower scores and asymmetries on the Y-balance test have been linked with an increased risk of injury.
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4 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
20 metre sprint
Periodo de tiempo: 4 months
|
Athletes will perform 3 trials of a 20 metre sprint, with their time at 10 m and 20 m recorded.
Timing will be done using a photo-electric timing system (SmartSpeed Pro, Fusion Sports, Chicago, USA).
Each subject will wear a radio-frequency identification (RFID) bracelet assigned at the Open House sign-in; this device will allow timing for the sprint test.
The fastest of the 3 trials will be used in analysis.
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4 months
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Multiple Jump test
Periodo de tiempo: 4 months
|
Athletes will perform 3 different types of jumps.
For each of the jumps the athlete stands on a Smart Jump Mat (SmartJump, Fusion Sports, Chicago, USA), and holds a dowel across the shoulders, behind the head.
A static jump requires the athlete to crouch down for a jump, pause at the bottom, and then jump as high as possible.
A countermovement jump requires the athletes to crouch down and immediately jump back up for maximum height.
Three submaximal practice trials of each jump will be done, followed by 3 test trials.
The goal is maximum vertical jump, measured by time in the air.
Then a series of elastic jumps, maximizing height but minimizing time on the mat, will be done for 60 seconds.
The athletes will have a short, submaximal practice trial first.
The jump tests will allow for a description of the athletes' power qualities, which are important for sport performance.
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4 months
|
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Functional Movement Screen score
Periodo de tiempo: 4 months
|
The FMS is a series of 7 tests including deep squat, hurdle step, in-line lunge, shoulder mobility, active straight leg raise, trunk stability push-up, and rotary stability tests.
The intent of the test is to screen athletes for the ability to complete functional activities that underlie more complex athletic skills.
A low score on the FMS has been related to increased injury risk.
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4 months
|
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Self-reported injury rates
Periodo de tiempo: 4 months
|
Injury rates will be recorded during the study period by asking parents to contact the researcher when an injury occurs.
A research assistant will also make bi-weekly phone calls to the parents/athletes in the study to ask about injury occurrence to ensure all injuries are noted.
The type of injury (acute or overuse), involved body part, and treatment received will be documented as reported by the parent.
No health identification numbers will be collected or healthcare practitioners contacted.
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4 months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Joanne Parsons, PhD, University of Manitoba
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de noviembre de 2016
Finalización primaria (Actual)
9 de abril de 2017
Finalización del estudio (Actual)
1 de mayo de 2017
Fechas de registro del estudio
Enviado por primera vez
5 de octubre de 2016
Primero enviado que cumplió con los criterios de control de calidad
5 de octubre de 2016
Publicado por primera vez (Estimar)
7 de octubre de 2016
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
9 de mayo de 2017
Última actualización enviada que cumplió con los criterios de control de calidad
5 de mayo de 2017
Última verificación
1 de octubre de 2016
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- HS20030
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .