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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02043275
Other study ID # #E2013:015
Secondary ID CIHR
Status Completed
Phase N/A
First received January 20, 2014
Last updated January 20, 2014
Start date April 2013
Est. completion date December 2013

Study information

Verified date January 2014
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if jump landing mechanics in young female athletes can be improved with a resistance training intervention.


Description:

After initial baseline testing, athletes were randomly selected to receive upper body (control group) or lower body (intervention group) resistance training. Athletes attended supervised training sessions twice per week for 12 weeks, after which they were re-tested.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 10 Years to 14 Years
Eligibility Inclusion Criteria:

- at least one year experience playing organized sports

Exclusion Criteria:

- previous experience with resistance training

- any injury with a pain level of more than 3/10 on VAS

- any health condition that would preclude them from completing the training or testing

- previous experience using a Biodex dynamometer

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Anterior Cruciate Ligament Injury

Intervention

Other:
Leg training
Lower body resistance training twice per week for one hour each time.
Arm training
Upper body resistance training twice per week for one hour each time.

Locations

Country Name City State
Canada Faculty of Kinesiology and Recreation Management Winnipeg Manitoba

Sponsors (2)

Lead Sponsor Collaborator
University of Manitoba Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Landing Error Scoring System score from Baseline to 12 weeks. Baseline and 12 weeks No
Secondary Neuromuscular power of the hip abductors measured by a Biodex isokinetic dynamometer 12 weeks No
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