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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01591941
Other study ID # BCM06-0007
Secondary ID
Status Completed
Phase Phase 2
First received May 2, 2012
Last updated May 3, 2012
Start date June 2006
Est. completion date August 2007

Study information

Verified date May 2012
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

There is a large number of young women who sustain serious knee injuries from playing soccer. Female athletes are at high risk of knee injuries from soccer than males. We will conduct a research project to assess the effect of a warm-up on changing some of the movement patterns thought to contribute to these serious knee injuries.

It is hypothesized that a core position and control movement strategy (Core-PAC) group reduce biomechanical risk factors at the knee compared to a control after the training program.


Description:

There is a large number of young women who sustain serious knee injuries from playing soccer. Female athletes are at high risk of knee injuries from soccer than males. We will conduct a research project to assess the effect of a warm-up on changing some of the movement patterns thought to contribute to these serious knee injuries.

A core position and control movement strategy (Core-PAC) may be one method of modifying high-risk movements such as side-cutting. The Core-PAC is a simple method of getting the centre of mass (COM) closer to the plant foot or base of support (BOS). Moving the COM closer to the BOS may bias joint loading to the sagittal rather than the frontal and transverse planes, which often occurs in female athletes and poses a risk for ACL injury.

In this study, we will conduct a randomized controlled trial to compare a Core-PAC trained group to a control group for peak flexion angles and peak abduction moments at the knee during a side-cut and an unanticipated side-cut prior to kicking a soccer ball and a side-hop task after a six-week training program.

It is hypothesized that a Core-PAC group would have greater peak flexion angles and lower peak abduction moments at the knee compared to a control after the training program.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2007
Est. primary completion date August 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 14 Years to 17 Years
Eligibility Inclusion Criteria:

- 14-17 years of age;

- have no injuries for six weeks prior to testing;

- have no medical problems preventing them from participating in the study.

Exclusion Criteria:

- have a previous ACL injury or repair;

- have a back or lower limb injury that kept them from playing or training for greater than 30 days in the past year;

- presently using a supplemental exercise based program;

- have any medical or neurologic condition that would impair their ability to perform the tasks.

Study Design

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


Related Conditions & MeSH terms


Intervention

Other:
Core-PAC
Core position and control movement strategy (Core-PAC): Do warm-up prior to 6 weeks of regular soccer training for peak flexion angles and peak abduction moments at the knee during a side-cut (SC) and an unanticipated side-cut (USC) prior to kicking a soccer ball and a side-hop (SH) task.

Locations

Country Name City State
Canada Rehab Research Lab, GF Strong Rehab Centre Vancovuer British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak knee flexion angle and peak abduction moment Intervention group will be instructed to move from the trunk first during a series of athletic tasks. The Control group will be instructed to move with their usual athletic movements during the same tasks.
After 6 weeks of this training, subjects will be asked to return to the GF Strong Rehabilitation Center for biomechanical testing.
6 weeks No
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