- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT01063673
The Relation Between Running Patterns and Overuse Injuries in Runners
Přehled studie
Postavení
Podmínky
Detailní popis
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.
Typ studie
Zápis (Aktuální)
Kontakty a umístění
Studijní místa
-
-
-
Holstebro, Dánsko, 7500
- VIA UC
-
-
Northern Jutland
-
Aalborg, Northern Jutland, Dánsko, 9000
- Northern Orthopaedic Division, Aalborg University Hospital
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
Popis
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
Studijní plán
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
|---|
|
Active runners
Observational follow-up study on 39 runners
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
|
Injury defined as any musculoskeletal complaint of the lower extremity or back causing a restriction of running for at least 1 week.
Časové okno: a two-week period before the injury arises
|
a two-week period before the injury arises
|
Spolupracovníci a vyšetřovatelé
Vyšetřovatelé
- Vrchní vyšetřovatel: Sten Rasmussen, M.D., DrMSc, Orthopaedic Division, North Denmark Region, Aalborg Hospital - Aarhus University Hospital, Denmark
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- M-20110114
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .