- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01063673
The Relation Between Running Patterns and Overuse Injuries in Runners
Study Overview
Status
Conditions
Detailed Description
Running patterns are thought to have a major influence on the development of Running Related Injuries (RRI).
Worldwide, running is a sport practiced by many individuals to improve cardio-respiratory function, health and well-being. Although running positively contributes to health, there is also a risk of running related injuries (RRI). At best, the consequence of RRI´s is a periodic absence from physical activity, with the athlete returning to sport within weeks. In the worst case, the injury is a chronic painful condition, causing a sedentary lifestyle without physical activity. This is undesirable since physical inactivity increases the risk of lifestyle diseases and death.
In Denmark it is estimated that 4.500 deaths each year can be attributed directly to inactivity. Furthermore, inactivity leads to reduced quality of life compared to active persons. To avoid people getting a sedentary lifestyle prevention of RRI are necessary.
To define a prevention strategy, one must have knowledge about risk factors and causation. Many risk factors have been proposed. Among these, running patterns and foot type are thought to play a major role in the development of RRI. However, very few firm conclusions can be made based on the existing literature, often because of methodical problems. Consequently, it is suggested to design large scale prospective studies controlling for multiple variables. Furthermore, studies should differentiate between novice, elite and extreme runners. Thus, the study design in this project will take these suggestions into account.
The aim of the study is to investigate the association between running patterns and overuse injuries in runners.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Holstebro, Denmark, 7500
- VIA UC
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Northern Jutland
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Aalborg, Northern Jutland, Denmark, 9000
- Northern Orthopaedic Division, Aalborg University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- between 18 and 65 years old
- has a GPS-watch that can measure training data (Garmin Forerunner 205,305 or 405)
- has registered their training (if they have run) for a period of at least three months before the inclusion in the trial
- has an e-mail address
Exclusion Criteria:
- does not wish to keep a training diary
- has not registered training data in the follow-up period
- has had an injury in the leg within the last three months before baseline
- active with another tough sports, cf. American College of Sports Medicine
- psychic condition that does not allow participation
- cannot read or understand Danish
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Active runners
Observational follow-up study on 39 runners
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Injury defined as any musculoskeletal complaint of the lower extremity or back causing a restriction of running for at least 1 week.
Time Frame: a two-week period before the injury arises
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a two-week period before the injury arises
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Collaborators and Investigators
Investigators
- Principal Investigator: Sten Rasmussen, M.D., DrMSc, Orthopaedic Division, North Denmark Region, Aalborg Hospital - Aarhus University Hospital, Denmark
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- M-20110114
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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