NCT Number: NCT02927418
Strength Training for Injury Prevention
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.
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Notify MeKey information
Conditions
Age range
12 year–16 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Control
BehavioralPrimary outcomes
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Y-balance score
Time frame: 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.
Secondary outcomes
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20 metre sprint
Time frame: 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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Multiple Jump test
Time frame: 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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Functional Movement Screen score
Time frame: 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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Self-reported injury rates
Time frame: 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.
Sponsors and collaborators
Lead sponsor
University of Manitoba
Other
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2017
- Study completion
- 2017
- First posted
- Oct 7, 2016
- Registry last updated
- May 9, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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