- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01092286
Effect of Neuromuscular Warm-up on Injuries in Female Athletes
January 23, 2018 updated by: Cynthia LaBella, Ann & Robert H Lurie Children's Hospital of Chicago
Effect of Neuromuscular Warm-up on Injuries in Female Athletes in Urban Public High Schools: A Cluster-randomized Controlled Trial
The goal of the study is to determine effect of coach-led neuromuscular warm-up on non-contact, lower extremity (LE) injury rates among female athletes in a predominantly non-white public high school system.
The investigators hypothesized the warm-up would reduce non-contact LE injuries.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
We will recruit basketball and soccer coaches and their athletes from Chicago public high schools.
We will randomize teams to intervention and control groups.
We will train intervention coaches to implement a 20-minute neuromuscular warm-up and tracked training costs.
Control coaches will use their usual warm-up.
All coaches will report weekly athlete exposures (AEs) and injuries resulting in a missed practice/game.
Research assistants will interview injured athletes.
We will compare injury rates between control and intervention groups.
Study Type
Interventional
Enrollment (Actual)
1653
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Ann & Robert H. Lurie Children's Hospital of Chicago
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 80 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria for High School Students (initial part of study - completed)
- plays basketball or soccer for a Chicago public high school team
- coaches basketball or soccer for a Chicago public high school team
- female, age 14-20
Inclusion Criteria for coaches (current part of study):
- Willing to implement a new warm-up before their team's practices and games
- Willing to complete a pre- and post-season survey before and after using the warm-up program for one season (surveys are attached).
- Willing to complete a pre- and post-workshop test before and after the workshop (tests are attached).
- Willing to allow study personnel to observe their implementation of the warm-up at up to three team practices or games.
Exclusion Criteria for coaches (current part of study) There are no separate exclusion criteria for coaches.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: neuromuscular warm-up
coaches in this arm use the prescribed warm-up before team practices
|
neuromuscular warm-up exercises that take 20 minutes to perform
Other Names:
|
|
No Intervention: no warm-up
coaches use their usual warm-up before team practices
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
lower extremity injury rates
Time Frame: one year
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
coach compliance with warm-up
Time Frame: one year
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cynthia R LaBella, MD, Ann & Robert H Lurie Children's Hospital of Chicago
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2006
Primary Completion (Actual)
July 1, 2009
Study Completion (Actual)
July 1, 2009
Study Registration Dates
First Submitted
March 23, 2010
First Submitted That Met QC Criteria
March 23, 2010
First Posted (Estimate)
March 24, 2010
Study Record Updates
Last Update Posted (Actual)
January 25, 2018
Last Update Submitted That Met QC Criteria
January 23, 2018
Last Verified
January 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB2006-12888
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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