Systematic, Comprehensive, One-to-One Training (SCOOT) for Scooter Skills: A Feasibility Study
7 oktober 2021 bijgewerkt door: Ben Mortenson, University of British Columbia
Systematic, Comprehensive, One-to-One Training (SCOOT) for Scooter Skills, is a novel, community-based, client-centred intervention where skills training is incorporated into social activities that users want to perform.
The trainer also offers problem solving strategies to help manage environmental barriers and to promote social participation.
This intervention is different from customary scooter training in that customary training is often very limited and focuses on learning discrete skills outside of the user's normal environment.
The purpose of this study is to explore the feasibility of conducting a mixed-methods, rater-blinded, randomized controlled trial (RCT) for new scooter users, which will evaluate the efficacy of SCOOT.
We anticipate that the feasibility outcomes will be strong enough to support the conduct of a subsequent multi-site trial with a sufficient sample size to enable us to quantify definitive outcomes such as adverse events (e.g., injuries and abandonment).
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
22
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
-
-
British Columbia
-
Vancouver, British Columbia, Canada, V5Z 2G9
- GF Strong Rehabilitation Center
-
-
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
60 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- English Speaking
- Aged 60 or above
- Has acquired a scooter in the last month prior to enrollment in the study
Exclusion Criteria:
- Has a cognitive impairment that will prevent the individual from providing consent and reliably completing the study questionnaires
- Reside in a nursing home
- Plan to move outside Vancouver within the next year
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: Ander
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: SCOOT Immediate
This group will receive SCOOT immediately
|
An occupational therapist trained by the principal investigator will perform 1.5 hour SCOOT sessions with participants one to two times a week over a period of 6 weeks.
SCOOT will provide instruction and practice for performing scooter skills (i.e., instruction on driving, basic and advanced scooter skills) that are embedded in self-selected activities that participants want to perform using their scooters.
|
|
Ander: SCOOT Delayed
This group will receive SCOOT after 6 weeks
|
An occupational therapist trained by the principal investigator will perform 1.5 hour SCOOT sessions with participants one to two times a week over a period of 6 weeks.
SCOOT will provide instruction and practice for performing scooter skills (i.e., instruction on driving, basic and advanced scooter skills) that are embedded in self-selected activities that participants want to perform using their scooters.
Participants will begin the SCOOT intervention after a six week delay.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change in scooter skills capacity
Tijdsspanne: Change from baseline skill level at 6 weeks, 12 weeks, 6 months, and 1 year
|
The WST-ScQ measures the participant's subjective scooter skills (capacity), and inquires on the frequency the skill is performed, and whether or not improvement of the skill is a personal goal.
|
Change from baseline skill level at 6 weeks, 12 weeks, 6 months, and 1 year
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Wheelchair Skills Test for Scooters (WST-Sc)
Tijdsspanne: Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
The WST-Sc consists of 29 skills that are scored by an examiner from 0 to 2, where 0 = unsafe or unable, 1 = safe with difficulty, and 2 = safe without difficulty
|
Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
|
Wheelchair Skills Test for Scooters - Questionnaire (WST-ScQ) (performance and confidence)
Tijdsspanne: Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
The WST-ScQ measures the participant's subjective scooter skills, and inquires on the participant's scooter skill confidence, frequency the skill is performed (performance), and whether or not improvement of the skill is a personal goal.
|
Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
|
Scooter Skills Confidence Questionnaire
Tijdsspanne: Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
This measure evaluates the participant's confidence in managing their social environment
|
Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
|
Wheeled Mobility Outcome Questionnaire
Tijdsspanne: Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
This measure evaluates indoor and outdoor participation levels associated with wheeled mobility provision by using an 11 point scale (0 = completely unsatisfied to 10 = completely satisfied).
|
Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
|
Life Space Assessment (LSA) Questionnaire
Tijdsspanne: Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
The LSA measures participants' frequency and independence of mobility in increasingly larger life spaces over the past month.
|
Baseline, at 6 weeks, 12 weeks, 6 months, and 1 year
|
|
Scooter Use and Incidents
Tijdsspanne: Baseline, 6 weeks, 12 weeks, 6 months, and 1 Year
|
Participants will be asked to keep a diary of any scooter-related adverse events, including the following: tips or falls from the scooter, injuries to self, accidental contact with others, injuries to others, and damage to property.
Participants will be asked to record the number of hours per day that they use their scooters.
|
Baseline, 6 weeks, 12 weeks, 6 months, and 1 Year
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Montreal Cognitive Assessment Test
Tijdsspanne: Baseline
|
This assessment is used to detect any mild cognitive impairments
|
Baseline
|
|
Late Life Functioning and Disability measure - Computer Assisted Testing (LLFDI - CAT)
Tijdsspanne: Baseline
|
The LLFDI-CAT is a computerized program that measures the participant's physical function.
Drawing from a bank of 141 items, CAT continues until a standard error of 3 is obtained for the domain score, or a maximum of ten items has been administered.
|
Baseline
|
|
Hearing Handicap Inventory for the Elderly (HHIE) Screening version
Tijdsspanne: Baseline
|
The HHIE will be used to evaluate the participants' hearing abilities.
|
Baseline
|
|
Scooter Physical Accessibility of Participant Home and Community
Tijdsspanne: Baseline
|
This measure involves 14 yes/no questions inquiring about the accessibility of the participants' physical environment in their home and community.
|
Baseline
|
|
Trail Making B Test
Tijdsspanne: Baseline
|
This task is used to measure the participants' visual attention and task switching abilities, which is related to on road driving
|
Baseline
|
|
Snellen Eye Test
Tijdsspanne: Baseline
|
Baseline
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Ben Mortenson, University of British Columbia
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
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 maart 2016
Primaire voltooiing (Werkelijk)
1 december 2020
Studie voltooiing (Werkelijk)
1 oktober 2021
Studieregistratiedata
Eerst ingediend
23 februari 2016
Eerst ingediend dat voldeed aan de QC-criteria
25 februari 2016
Eerst geplaatst (Schatting)
2 maart 2016
Updates van studierecords
Laatste update geplaatst (Werkelijk)
11 oktober 2021
Laatste update ingediend die voldeed aan QC-criteria
7 oktober 2021
Laatst geverifieerd
1 oktober 2021
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- H15-01921
- F15-00959 (Ander subsidie-/financieringsnummer: Canadian Institutes of Health Research)
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 .