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Strength Training for Injury Prevention

Primary Purpose

Wounds and Injuries

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Strength & Conditioning
Control
Sponsored by
University of Manitoba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Wounds and Injuries

Eligibility Criteria

12 Years - 16 Years (Child)All SexesAccepts Healthy Volunteers

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Strength & Conditioning

    Control

    Arm Description

    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.

    Athletes in the control group will continue with their usual sports and activities but will not receive any type of training.

    Outcomes

    Primary Outcome Measures

    Y-balance score
    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.

    Secondary Outcome Measures

    20 metre sprint
    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.
    Multiple Jump test
    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.
    Functional Movement Screen score
    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.
    Self-reported injury rates
    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.

    Full Information

    First Posted
    October 5, 2016
    Last Updated
    May 5, 2017
    Sponsor
    University of Manitoba
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02927418
    Brief Title
    Strength Training for Injury Prevention
    Official Title
    Strength Training for Injury Prevention
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    November 2016 (Actual)
    Primary Completion Date
    April 9, 2017 (Actual)
    Study Completion Date
    May 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Manitoba

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Wounds and Injuries

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Non-Randomized
    Enrollment
    43 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Strength & Conditioning
    Arm Type
    Experimental
    Arm Description
    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.
    Arm Title
    Control
    Arm Type
    Active Comparator
    Arm Description
    Athletes in the control group will continue with their usual sports and activities but will not receive any type of training.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Strength & Conditioning
    Intervention Type
    Behavioral
    Intervention Name(s)
    Control
    Primary Outcome Measure Information:
    Title
    Y-balance score
    Description
    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.
    Time Frame
    4 months
    Secondary Outcome Measure Information:
    Title
    20 metre sprint
    Description
    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.
    Time Frame
    4 months
    Title
    Multiple Jump test
    Description
    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.
    Time Frame
    4 months
    Title
    Functional Movement Screen score
    Description
    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.
    Time Frame
    4 months
    Title
    Self-reported injury rates
    Description
    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.
    Time Frame
    4 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    12 Years
    Maximum Age & Unit of Time
    16 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    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
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Joanne Parsons, PhD
    Organizational Affiliation
    University of Manitoba
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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