- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT03641066
Progressing Ankle Brace Restriction on Walking and Running Gait Characteristics in Healthy Individuals
22 maart 2019 bijgewerkt door: Sport and Spine Rehab Clinical Research Foundation
The Effect of Progressing Ankle Brace Restriction on Walking and Running Gait Characteristics in Healthy Individuals
A convenience sample of 20 participants, 18 years or older healthy individuals were recruited.
Participants were excluded if they report being pregnant or being treated for a musculoskeletal injury.
After explanation of the study and consent were obtained, each participant completed background information and the Cumberland Ankle Instability Tool (CAIT).
Participants began by completing a 1 minute, 3mph walking gait assessment while unbraced, followed by a 2-minute, 6mph unbraced running assessment.
Following the unbraced condition participants were randomly assigned into 1 of 4 conditions: [1] Active Ankle 329 Ankle Sleeve, [2] AS1Pro, [3] Eclipse 1, or [4] Eclipse 2. Participants placed an assigned brace on each ankle and then repeated the walking gait and running assessments.
After this test the participants filled out a 10-item satisfaction questionnaire, and then were randomly assigned a second brace.
The protocol was repeated until they have completed the walking, running, and satisfaction survey in all 4 brace conditions.
Studie Overzicht
Gedetailleerde beschrijving
A convenience sample of 20 participants, 18 years or older healthy individuals were recruited.
Participants were excluded if they report being pregnant or being treated for a musculoskeletal injury.
After explanation of the study and consent were obtained, each participant completed background information and the Cumberland Ankle Instability Tool (CAIT).
Participants began by completing a 1 minute, 3mph walking gait assessment while unbraced, followed by a 2-minute, 6mph unbraced running assessment.
Following the unbraced condition participants were randomly assigned into 1 of 4 conditions: [1] Active Ankle 329 Ankle Sleeve, [2] AS1Pro, [3] Eclipse 1, or [4] Eclipse 2. Participants placed an assigned brace on each ankle and then repeated the walking gait and running assessments.
After this test the participants filled out a 10-item satisfaction questionnaire, and then were randomly assigned a second brace.
The protocol was repeated until they have completed the walking, running, and satisfaction survey in all 4 brace conditions.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
20
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
-
-
Maryland
-
Rockville, Maryland, Verenigde Staten, 20852
- Sport & Spine Rehab
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- healthy individuals who are able to run for 10 minutes total
Exclusion Criteria:
- pregnancy, lower body injury
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Fundamentele wetenschap
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
---|---|
Experimenteel: Ankle Brace
Each participant will complete a baseline analysis of 1 minute of walking and 2 minutes of running, repeated 4 more times wearing 4 different braces.
The analysis will be completed on the Walker View Treadmill, which used 3D camera technology to capture lower body kinematics.
The treadmill also has load cells built in to capture gait characteristics
|
Each participant will complete the 1 minute walking and 2 minute running under 5 conditions [1] un-braced, [2] Active Ankle 329 Ankle Sleeve, [3] AS1Pro (a lace-up brace), [4] Eclipse 1 (single-upright brace), and [5] Eclipse 2 (double upright brace)
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Change in Ankle Dorsiflexion/Plantarflexion Range of Motion
Tijdsspanne: Ankle Dorsiflexion/Plantarflexion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Ankle Dorsiflexion/Plantarflexion Range of Motion will be measured using the Woodway Walker View Treadmill which utilizes a 3D camera
|
Ankle Dorsiflexion/Plantarflexion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Change in Ankle Inversion/Eversion Range of Motion
Tijdsspanne: Ankle Inversion/Eversion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Ankle Inversion/Eversion Range of Motion will be measured using the Woodway Walker View Treadmill which utilizes a 3D camera
|
Ankle Inversion/Eversion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Change in Knee Flexion Range of Motion
Tijdsspanne: Knee Flexion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Knee Flexion Range of Motion will be measured using the Woodway Walker View Treadmill which utilizes a 3D camera
|
Knee Flexion Range of Motion will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Change in Step Length
Tijdsspanne: Step Length will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Step Length will be measured using the Woodway Walker View Treadmill which utilizes load cells within the treadmill belt
|
Step Length will be measured for the last 30 seconds of the 1 minute walk, and the last 30 seconds of the 2 minute run. It will be measured during each of the 5 conditions.
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 april 2018
Primaire voltooiing (Werkelijk)
1 september 2018
Studie voltooiing (Werkelijk)
1 januari 2019
Studieregistratiedata
Eerst ingediend
2 juli 2018
Eerst ingediend dat voldeed aan de QC-criteria
17 augustus 2018
Eerst geplaatst (Werkelijk)
21 augustus 2018
Updates van studierecords
Laatste update geplaatst (Werkelijk)
25 maart 2019
Laatste update ingediend die voldeed aan QC-criteria
22 maart 2019
Laatst geverifieerd
1 maart 2019
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- AnkleBrace Running
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
Klinische onderzoeken op Ankle Brace
-
The Catholic University of KoreaOnbekendNiet-kleincellige longkankerKorea, republiek van