- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04789369
Fear of Movement, Functionality and Quality of Life in Elite Athletes With an Ankle Instability History
2. juni 2022 opdateret af: Özgül Öztürk, Acibadem University
The Relationship Between Fear of Movement, Functionality and Quality of Life in Elite Athletes With an Ankle Instability History
Ankle sprain is frequently experienced by individuals participating in different sports activities.
Ankle sprains have been shown to result in a decrease in level of physical activity and persistence of some symptoms for a long time.
In this case, it is predicted that ankle sprains may affect the quality of life as well as functionality.
Also, ankle sprain history may result in increased fear of movement, which may delay return to sports.
This study aimed to examine the relationship between foot and ankle functionality, fear of movement and quality of life of elite athletes with a history of ankle sprain.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
80
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Istanbul, Kalkun
- Sportomed Fulya Physiotherapy Center
-
-
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 35 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
Athletes who are participating in sportive activities regularly
Beskrivelse
Inclusion Criteria:
- No injury to the upper or lower extremities during data collection,
- Being older than 18 years of age,
- Individuals who volunteer to participate.
Exclusion Criteria:
. Having had ankle surgery,
- Has had an injury to his lower extremity in the last 3 months,
- Individuals with a history of neurological / neuropsychiatric disease or arthritis will be excluded from the study.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Foot and Ankle Ability Measure
Tidsramme: 1 day
|
The Foot and Ankle Ability Measure will be used to determine the ankle functionality.
This scale was developed to determine lower extremity functional level.
It evaluates the level of difficulty of the person in activities in daily life in 21 items with a 5-point Likert-type scale, which means "4 = not difficult at all" and "0 = I cannot do it".
At the same time, it can be reported within the scope of the scale that the specified activity cannot be implemented.
High score means better functions.
|
1 day
|
|
Short Form-12
Tidsramme: 1 day
|
Short-Form 12 is a valid and reliable scale for determining the level of quality of life.
This scale consists of 12 items and can be scored as 8 subscales which are physical function, restricted roles due to physical problems, pain, general health, energy / vitality, social functions, mental health and mental health with restricted roles due to emotional problems.
All items are evaluated with a 5-point Likert-type scale, and higher scores indicate better quality of life.
|
1 day
|
|
Fear Avoidance Beliefs Questionnaire
Tidsramme: 1 day
|
The FABQ measures athletes' fear of pain and consequent avoidance of physical activity or sports because of their increased fear.
The questionnaire contains 16 items between 0 and 6 while 0 indicates completely disagree and 6 indicates completely agree.
The maximum score is 96 and higher scores indicates increased level of fear avoidance beliefs.
|
1 day
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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)
15. marts 2021
Primær færdiggørelse (Faktiske)
15. maj 2022
Studieafslutning (Faktiske)
30. maj 2022
Datoer for studieregistrering
Først indsendt
5. marts 2021
Først indsendt, der opfyldte QC-kriterier
5. marts 2021
Først opslået (Faktiske)
9. marts 2021
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
3. juni 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
2. juni 2022
Sidst verificeret
1. juni 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2020-04/14
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
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 .