- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04083391
Flexibility Deficit in Chronic Ankle Instability
5. september 2019 opdateret af: Abd Elhady Samy Abu Mandour, Cairo University
Is Hamstring Flexibility Affected in Chronic Ankle Instability
chronic ankle instability could be associated with some proximal deficits as in hip and knee regions.
these deficits include alternations in motor neurons pools excitability, muscle strength, kinematics and kinetics.
this study add muscle inflexibility to the preciouse literature.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Background: influence of a localized injury in a distal joint on the function of proximal muscles is an important consideration in assessment and treatment of musculoskeletal injuries.
Up to the investigator's knowledge, there is no study assess flexibility changes in CAI.
Objectives: The objective of this study is to investigate Hamstring flexibility in CAI.
Material and methods: The study conducted on 42 subjects with unilateral CAI and controls had measure of hamstring flexibility using digital inclinometer during passive knee extension test .Results: Revealed statistical and clinical significant difference between non-injured control group and CAI group with decreased hamstring flexibility in the later.
Conclusion: CAI subjects have proximal muscular affection include hamstring tightness which may alter sacroiliac joint stability and subsequently back pain.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
42
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
18 år til 30 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Outpatients clinic faculty of physical therapy Cairo university
Beskrivelse
Inclusion Criteria:
- The control group was self-reported to be healthy
- Had no ankle injury history
- Matched with CAI patients in gender, dominance side and simulated injured side
- CAI group had a self-report of a past history of unilateral ankle inversion injury since at least more than 1 year before the study onset which required a period of protected weight bearing and/or immobilization at least one day
- Patient reported a tendency for the ankle to give way and/or recurrent ankle sprain
- Perceives that the ankle was chronically weaker, more painful and/or less functional than the other ankle or than before first
Exclusion Criteria:
- Had a history of lower extremity injury
- Surgery or fracture
- History of low back dysfunction that required medical or surgical intervention within the last year, Current participation in formal or informal rehabilitation
- History of hamstring strain
- Bilateral ankle sprain injury
- Ankle injury within 3 months of participation
- History of ankle fracture and any neuromuscluskeletal disease could affect the condition.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: Case-Control
- Tidsperspektiver: Tværsnit
Kohorter og interventioner
Gruppe / kohorte |
---|
CAI group
assessment had been done to this group that include patients with ankle sprain injury from more than one year and complain with repetitive injuries, giving way and instability feelings
|
non injured ankle group
assessment had been done to this group that include control participants had not injured their ankle before and matched with CAI in age, gender, dominant side
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Hamstring muscle flexibility
Tidsramme: throughout the study average 1 year
|
angle between tibia and femur during passive knee extension test
|
throughout the study average 1 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studiestol: Afaf Tahoon, Master, assistant lecturer faculty of physical therapy Cairo university
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)
7. maj 2016
Primær færdiggørelse (Faktiske)
30. december 2016
Studieafslutning (Faktiske)
9. marts 2017
Datoer for studieregistrering
Først indsendt
23. august 2019
Først indsendt, der opfyldte QC-kriterier
5. september 2019
Først opslået (Faktiske)
10. september 2019
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
10. september 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. september 2019
Sidst verificeret
1. september 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- P.T.REC/012/001312
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Ingen
IPD-planbeskrivelse
IPD had been planed to be shared with research team only through specific username and password
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
produkt fremstillet i og eksporteret fra U.S.A.
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Kronisk ankelinstabilitet
-
Jules Bordet InstituteMacopharma; Belgian Hematological SocietyRekrutteringRefractory Chronic Graft Versus Host Disease (cGVHD)Belgien
-
La Tour HospitalAfsluttetSkuldersmerter | Skulderluksation | Joint Instability Syndrome
-
Eli Lilly and CompanyAktiv, ikke rekrutterendeKræft i bugspytkirtlen | Solid tumor | Kutant melanom | Microsatellite Instability-High (MSI-H) solide tumorer | Brystkræft (HR+HER2-)Belgien, Spanien, Korea, Republikken, Forenede Stater, Taiwan, Frankrig, Canada
-
Third Affiliated Hospital, Sun Yat-Sen UniversityRekrutteringKolorektal cancer | Neoadjuverende terapi | Mismatch Repair-deficient (dMMR) | Microsatellite Instability-high (MSI-H)Kina
-
Sun Yat-sen UniversityRekrutteringKolorektal cancer | Neoadjuverende terapi | Mismatch Repair-deficient (dMMR) | Microsatellite Instability-high (MSI-H)Kina
-
LiuYingIkke rekrutterer endnuKolorektal cancer | Neoadjuverende terapi | Mismatch Repair-deficient (dMMR) | Microsatellite Instability-high (MSI-H)Kina
-
Sun Yat-sen UniversityRekrutteringKolorektal cancer stadium IV | Mismatch Repair-deficient (dMMR) | Microsatellite Instability-high (MSI-H)Kina
-
Novartis PharmaceuticalsLedigPrimær myelofibrose (PMF) | Polycytæmi Vera (PV) | Post polycytæmi myelofibrose (PPV MF) | Trombocytæmi myelofibrose (PET-MF) | Alvorlig/meget svær COVID-19 sygdom | Steroid Refractory Acute Graft Versus Host Disease (SR aGVHD) | Steroid Refractory Chronic Graft Versus Host Disease (SR cGVHD)
-
Incyte Biosciences International SàrlAfsluttetLivmoderhalskræft | Hepatocellulært karcinom | Spiserørskræft | Livmoderhalskræft | Mesotheliom | Ikke-småcellet lungekræft (NSCLC) | Urothelialt karcinom | Merkel cellekarcinom | Diffust storcellet B-celle lymfom | Triple-negativ brystkræft | Nyrecellekarcinom (RCC) | Småcellet lungekræft (SCLC) | Planocellulært karcinom... og andre forholdForenede Stater