- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03447652
En undersøgelse, der undersøger virkningerne af et ankelrehabiliteringsprogram på gymnasieatleter med ankelustabilitet
12. oktober 2018 opdateret af: Mary Spencer Cain, Georgia State University
Et randomiseret kontrolleret forsøg, der undersøger virkningerne af et 4-ugers ankelrehabiliteringsprogram på gymnasieatleter med kronisk ankelustabilitet
Et randomiseret kontrolleret forsøg, der undersøger virkningerne af et 4-ugers ankelrehabiliteringsprogram på gymnasieatleter med kronisk ankelinstabilitet.
Studieoversigt
Status
Afsluttet
Detaljeret beskrivelse
Et randomiseret kontrolleret forsøg, der undersøger virkningerne af tre forskellige 4-ugers ankelrehabiliteringsprogrammer på gymnasieatleter med kronisk ankelinstabilitet.
Vi vil bruge spørgeskemaer til at vurdere subjektivt funktionsniveau og kliniske mål til at vurdere klinisk funktionalitet via statisk og funktionel balance.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
43
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Georgia
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Atlanta, Georgia, Forenede Stater, 30327
- Holy Innocents' Episcopal School
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Atlanta, Georgia, Forenede Stater, 30327
- The Lovett School
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Atlanta, Georgia, Forenede Stater, 30327
- The Westminister Schools
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College Park, Georgia, Forenede Stater, 30337
- Woodward Academy
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Decatur, Georgia, Forenede Stater, 30030
- Decatur High School
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Marietta, Georgia, Forenede Stater, 30062
- The Walker School
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Marietta, Georgia, Forenede Stater, 30062
- Walton High School
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
15 år til 18 år (Barn, Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inklusionskriterier:
- aktiv i mindst 1,5 time om ugen, en historie med mindst 1 betydelig ankelforstuvning, der krævede medicinsk indgriben, gentagne symptomer på smerte, hævelse, svaghed, ustabilitet og gentagne episoder med at give efter.
Ekskluderingskriterier:
- tilstedeværelse af enhver aktuel underekstremitetsskade (diagnosticeret af en læge inden for de sidste 3 måneder med nuværende symptomer), tidligere operation i begge ben, diagnosticeret ankelforstuvning inden for de seneste 6 uger, anamnese med ankelbrud og/eller dislokationer.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Ingen indgriben: Kontrolgruppe
Hver patient i kontrolgruppen udførte ikke nogen rehabiliteringsøvelser.
I løbet af interventionsperioden blev patienten forpligtet til at tjekke ind med et medlem af forskerholdet hver uge for at diskutere eventuelle ændringer i deres ankel eller rapportere enhver skadeshyppighed.
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Eksperimentel: Modstandsbandgruppen
Hver session gennemførte patienterne modstandstræning ved hjælp af et modstandsbånd i 4 retninger af ankelbevægelse (plantarfleksion, dorsalfleksion, inversion og eversion).
Patienterne ville gennemføre 3 sæt af 10 gentagelser under hver session.
Hver 3 session ville båndmodstanden øges.
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Resistance Band - bruger et spændingsbånd til at give modstand under ankelbevægelser
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Eksperimentel: Biomekanisk ankelplatformssystem
Det biomekaniske ankelplatformsystembræt er et ovalt bræt, der bruger en halvkugle i bunden af brættet, så patienten kan træne på en ustabil overflade.
En etbensstilling på deres involverede lem blev udført på det biomekaniske ankelplatforms systemkort, mens cirkler med uret og mod uret blev fuldført.
Den indledende retningsrotation blev valgt af patienten og ændret hvert 10. sekund af det 40 sekunder lange forsøg.
Fem forsøg på 40 sekunder blev afsluttet med 1 minuts hvileintervaller mellem forsøgene.
Progression blev bestemt af den superviserende kliniker og var baseret på patientens evne til at lave jævne overgange mellem retningsændringer og afslutning af jævne cirkulære rotationer i begge retninger.
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Biomekanisk ankelplatform systemkortgruppe - bruger forskellige niveauer af halvkugler for at øge mængden af tilladt bevægelse ved anklen.
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Eksperimentel: Kombinationsgruppe
Patienter, der fuldførte kombinationsprotokollen, gennemførte både modstandsbåndet og biomekanisk ankelplatforms systemkortprotokoller under hver session.
Rækkefølgen for afslutning af øvelsen blev udlignet for hver session.
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Kombinationsgruppe - inkluderer programmerne både modstandsbåndet og biomekanisk ankelplatformsystem.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Statiske balancevurderinger
Tidsramme: 4 uger
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Statisk balance kliniske tests
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4 uger
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Funktionelle balancevurderinger
Tidsramme: 4 uger
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Funktionel balance kliniske tests
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4 uger
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Patient selvrapporterede resultater
Tidsramme: 4 til 12 uger
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Spørgeskemaer til subjektive patientrapporterede resultater
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4 til 12 uger
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Studieleder: Benjamin M Goerger, PhD, Georgia State University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
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- Carcia CR, Martin RL, Drouin JM. Validity of the Foot and Ankle Ability Measure in athletes with chronic ankle instability. J Athl Train. 2008 Apr-Jun;43(2):179-83. doi: 10.4085/1062-6050-43.2.179.
- Wikstrom EA, Hubbard-Turner T, McKeon PO. Understanding and treating lateral ankle sprains and their consequences: a constraints-based approach. Sports Med. 2013 Jun;43(6):385-93. doi: 10.1007/s40279-013-0043-z.
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Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
14. august 2017
Primær færdiggørelse (Faktiske)
13. august 2018
Studieafslutning (Faktiske)
30. august 2018
Datoer for studieregistrering
Først indsendt
28. januar 2018
Først indsendt, der opfyldte QC-kriterier
26. februar 2018
Først opslået (Faktiske)
27. februar 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. oktober 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. oktober 2018
Sidst verificeret
1. oktober 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CON006264
Plan for individuelle deltagerdata (IPD)
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Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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Studerer et amerikansk FDA-reguleret enhedsprodukt
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