Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02927418
Other study ID # HS20030
Secondary ID
Status Completed
Phase N/A
First received October 5, 2016
Last updated May 5, 2017
Start date November 2016
Est. completion date May 2017

Study information

Verified date October 2016
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date May 2017
Est. primary completion date April 9, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 16 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Strength & Conditioning

Control


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Manitoba

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 4 months
Secondary 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. 4 months
Secondary 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. 4 months
Secondary 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. 4 months
Secondary 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. 4 months
See also
  Status Clinical Trial Phase
Recruiting NCT04554212 - Blood Flow Restriction Training After Patellar INStability N/A
Suspended NCT02932176 - Machine Learning for Handheld Vascular Studies
Recruiting NCT04803253 - Study of the Social and Professional Reintegration Improvements Using a Set of Solutions for Upper Limb Amputation N/A
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Completed NCT03463720 - Outcome for Patients With War-Associated Extremity Wound Infection N/A
Completed NCT03113253 - TRANexamic Acid to Reduce Bleeding in BURN Surgery Phase 4
Not yet recruiting NCT05492903 - COMmunity of Practice And Safety Support for Navigating Pain (COMPASS-NP) N/A
Terminated NCT02909231 - One-year Patient Reported Outcomes Following Hospitalization for Trauma N/A
Completed NCT02432456 - Ketamine Infusion Therapy for the Management of Acute Pain in Adult Rib Fracture Patients Phase 4
Completed NCT02266771 - Impact of V.A.C. Veraflo Therapy in Wounds Requiring Debridement Within an Orthopedic Practice N/A
Completed NCT02744144 - Wound Bacterial Microbiota and Their Antibiotic Resistance N/A
Completed NCT02394821 - Odor Management in Fungating Wounds Comparing Metronidazole and Polihexanide Phase 3
Not yet recruiting NCT01665963 - Efficacy of TopClosure(C)System in Healing Complicated Pacemaker Wounds N/A
Completed NCT00151112 - Comparison of Two Different Procedures for Plexus Anesthesia N/A
Not yet recruiting NCT03872544 - Short Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Recruiting NCT04596124 - Effectiveness and Tolerability of Fitostimoline Plus Cream and Gauze vs Connettivina Bio Plus Cream and Gauze N/A
Recruiting NCT05800834 - Benefits of Morphine Gel for Pain Reduction in Patients With Cancer Wounds Phase 2
Enrolling by invitation NCT03880188 - Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Terminated NCT04775316 - Prospective, International, Multicenter, Observational Study to Evaluate the Clinical Performance and Safety of a Silicone-coated Transparent Postoperative Dressing
Enrolling by invitation NCT03312504 - Implementing a School Prevention Program to Reduce Injuries Through Neuromuscular Training N/A