- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01063673
The Relation Between Running Patterns and Overuse Injuries in Runners
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
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.
Tipo di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
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Holstebro, Danimarca, 7500
- VIA UC
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Northern Jutland
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Aalborg, Northern Jutland, Danimarca, 9000
- Northern Orthopaedic Division, Aalborg University Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
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Active runners
Observational follow-up study on 39 runners
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
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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.
Lasso di tempo: a two-week period before the injury arises
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a two-week period before the injury arises
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Sten Rasmussen, M.D., DrMSc, Orthopaedic Division, North Denmark Region, Aalborg Hospital - Aarhus University Hospital, Denmark
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- M-20110114
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .