- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04050319
ATI Evidence-based Guide Investigating Medical and Preventative Services
ATI Evidence-based Guide Investigating Medical and Preventative Services: Sports Medicine, Athletic Training and Physical Therapy Treatment, Return to Sport, and Outcomes Registry
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The investigators goal is to provide a mechanism that allows for a better understanding of athlete management from injury prevention through maintenance of health or development of injury and rehabilitation. The goal is to describe best practice for prevention and treatment to maximize return to health, sport, and patient reported outcomes following time. This includes collection of pre-existing risk factors, prevention program participation, treatment initiatives, functional outcomes measured by standardized and validated tools from the published literature. It incorporates comorbidities and patient demographic characteristics. All of these components come together to form a remarkably comprehensive picture of athlete health, influencing factors, and their associated outcomes.
Data are collected via the athletic training electronic medical record system EMR and integrated with data from the investigators proprietary EMR system and are genuine to the community through clinical process. The data are collected in real-time with athletes and patients and the scores are immediately provided to the providing athletic trainer and therapist as well as archived for later Registry and scientific use.
Subsequent reporting can be adjusted to any variable collected which yields robust insights as to athlete health. However, no PHI information will be available.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Illinois
-
Bolingbrook, Illinois, United States, 60440
- ATI
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Active in an Organized Sports Team,
Exclusion Criteria: None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
DASH - Disabilities of the Arm, Shoulder, and Hand
Time Frame: through study completion, an average of 1 year
|
Subjective
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Chris Stout, PsyD, ATI
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SOR08012019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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