Effectiveness of a Wheelchair Skills Training Program for Power Mobility Users: A Randomized Controlled Trial

NCT ID: NCT01432418

Last Updated: 2016-05-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

116 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-06-30

Study Completion Date

2014-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a 3-year multi-centre, single-blinded, randomized controlled trial (RCT) to test the hypothesis that wheelchair skills training (using a systematic training program called the Wheelchair Skills Training Program) improves wheelchair skills and safety of 144 powered wheelchair users. A second objective is to assess the effects of age, sex, training centre, and participant experience on outcomes, assessing the retention of benefits and assessing the impact of training on other important outcomes.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Movement Disorders

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

wheelchair training

Group Type EXPERIMENTAL

Wheelchair skills training program

Intervention Type OTHER

A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.

Control

Standard of care only

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Wheelchair skills training program

A training program that uses methods based on the rehabilitation, wheelchair, and motor skills literature to teach wheelchair skills.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* new or experienced powered wheelchair users
* use or are expected to use powered wheelchairs for at least 4 hrs/week
* have access to a powered wheelchair with a suitable range of controller settings (i.e. able to climb a 5cm level change) for testing and training
* equal or greater than 18 years of age
* able to follow directions in either French or English (whichever is in use at the participating site)
* have the potential to operate their powered wheelchairs independently
* have room for improvement (in the opinion of the potential participant's clinician)
* requires no more than minimal assistance for communication and auditory comprehension (in the opinion of the potential participant's clinician)
* able to follow 2-step commands
* demonstrate the ability to attend training sessions during the intake session
* competent to provide their own informed consent
* able to be comfortably seated in the powered wheelchairs that will be used for the study (if not their own).

Exclusion Criteria

* use or are expected to use a scooter
* have a rapidly progressive disorder (e.g. amyotrophic lateral sclerosis or terminal cancer)
* have significant visual impairments (legally blind)
* have unstable medical conditions (e.g. angina, seizures)
* have emotional problems (e.g. severe anxiety, depression) that might make participation unsafe or unpleasant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

Sponsor Role collaborator

Nova Scotia Health Authority

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Lee Kirby

Attending Staff Physician, Department of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Lee Kirby, MD, FRCP

Role: PRINCIPAL_INVESTIGATOR

Nova Scotia Health Authority

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

GFS Rehabilitation Centre

Vancouver, British Columbia, Canada

Site Status

Nova Scotia Rehabilitation Centre

Halifax, Nova Scotia, Canada

Site Status

University of Western Ontario

London, Ontario, Canada

Site Status

Toronto Rehab

Toronto, Ontario, Canada

Site Status

Centre de Réadaptation Lucie-Bruneau

Montreal, Quebec, Canada

Site Status

Centre Interdisciplinaire de Recherche en Réadaptation et Intégration Sociale

Québec, Quebec, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CDHA-RS/2012-133

Identifier Type: OTHER

Identifier Source: secondary_id

230378

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Dual-task Training in Older Adults
NCT05296551 TERMINATED NA
Attention Training
NCT01518738 COMPLETED NA