- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07798869
Genu Varum, Change of Direction, and Reactive Agility in Youth Football Players
Does Genu Varum Influence Change of Direction and Reactive Agility Performance in Youth Football Players?
The goal of this observational study is to compare change-of-direction (COD) and reactive agility (RA) performance between football players with and without genu varum and to examine whether lower-limb alignment is associated with these performance measures.
The main questions it aims to answer are:
- Do football players with and without genu varum differ in COD and RA performance?
- Is lower-limb alignment associated with COD and RA performance in football players with and without genu varum?
Football players with and without genu varum will undergo assessments of lower-limb alignment, COD performance, and RA performance. The study will compare performance between the two groups and examine the relationship between lower-limb alignment and performance measures.
Studieoversikt
Status
Forhold
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
-
-
Antalya, Tyrkia (Türkiye)
- Akdeniz University
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
Tar imot friske frivillige
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- At least five years of football experience
- Participation in football training at least five days per week
- Voluntary participation in the study
Exclusion Criteria:
- History of lower extremity surgery
- Current musculoskeletal injury affecting performance
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
|
Genu Varum Group
Football players with genu varum who will be assessed for lower-limb alignment, change-of-direction performance, and reactive agility performance.
|
|
Control Group
Football players without genu varum who will be assessed for lower-limb alignment, change-of-direction performance, and reactive agility performance.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change-of-direction performance
Tidsramme: at basline
|
Change-of-direction performance will be assessed using the SpeedCourt system (Globalspeed GmbH, Hemsbach, Germany).
The test consists of a 14.5-m running course with four changes of direction.
Performance will be evaluated based on total completion time, with lower times indicating better change-of-direction performance.
|
at basline
|
|
Reactive agility performance
Tidsramme: at basline
|
Reactive agility performance will be assessed using the SpeedCourt system (Globalspeed GmbH, Hemsbach, Germany).
Participants will respond as quickly and accurately as possible to randomly presented visual stimuli and perform the required directional movements.
Performance will be evaluated based on total completion time, with lower times indicating better reactive agility performance.
|
at basline
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Intercondylar distance and intermalleolar distance
Tidsramme: at basline
|
Lower-limb alignment will be assessed by measuring intercondylar distance (ICD) and intermalleolar distance (IMD) in centimeters.
ICD will be measured as the distance between the medial femoral condyles, and IMD as the distance between the medial malleoli, using a standardized measurement procedure.
|
at basline
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2025-89
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .