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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05292690
Other study ID # 2020/MEDPHYS/01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 29, 2021
Est. completion date August 31, 2021

Study information

Verified date July 2022
Source East Kent Hospitals University NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Preliminary evaluation of an obstacle alerting system to enhance the user's independent mobility by improving their confidence to drive and their safety in driving a powered wheelchair.


Description:

Many powered wheelchair users find that collision free driving presents a significant challenge to confident and safe driving. In some cases so much so that the user will not drive their chair in some environments. Interviews with users in the EDUCAT project confirmed that users had problems driving safely and confidently in a confined space, passing through doorways or down narrow corridors and when reversing. Therefore the goal of this stage of the project is to improve the quality of life of the powered chair user by developing an obstacle alerting system which will help improve their confidence and safety in driving. This was to be achieved by asking expert users to provide feedback on the impact and usefulness of providing information about the presence and location of obstacles in the vicinity of their powered wheelchair. There are two aspects to this. 1. User assessment of the usefulness of the obstacle alerting feedback. This will include user evaluation of the value of the different modes of feedback - audio, visual and haptic - and how best to adapt these to the range of driving environments and driving speeds. And what level of control the user requires to select and deselect these options. 2. Monitoring the user's driving patterns with and without obstacle alerting -using the Stage 1 recording device. The analysis of this data, and feedback from the Users and carers will inform the development and design of the obstacle alerting system. Because of the COVID-19 pandemic the trial could not be carried out with powered wheel-chair users participating as they represented a clinically vulnerable part of the population. The trial was, therefore, adapted and carried out with adult non-wheelchair users.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date August 31, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: 1. Adults who are not wheelchair users. 2. Willing and able to provide a valid consent. 3. Able to participate in interviews aided or unaided using preferred method of communication. 4. Willing to drive a powered chair. Exclusion Criteria: 1. Lacks capacity to consent

Study Design


Intervention

Device:
Powered Wheelchair Obstacle Alerting System
Evaluation of an Obstacle Alerting System

Locations

Country Name City State
United Kingdom East Kent Hospitals NHS Foundation Trust Canterbury Kent

Sponsors (5)

Lead Sponsor Collaborator
East Kent Hospitals University NHS Foundation Trust KU Leuven, l'Institut supérieur de l'électronique et du numérique (ISEN) Lille, Sussex Community NHS Foundation Trust, University of Kent

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pre-trial Participant Evaluation of the possible Value of an Obstacle Alerting System The participant had been given an information sheet describing the Obstacle Alerting System.
The participants were given the pre-trial questionnaire to obtain their opinion of the value of the Obstacle Alerting System.
In a face to face interview the participants were asked to score each question. 0=don't know, 1=not at all, to 5=very helpful. Participants were also asked to discuss the reasons for their choices.
Questions included. Value of warning of obstacles in the vicinity of the powered chair. Use of visual, auditory and haptic feedback in a range of environments e.g. small room, lifts, corridor, doorways, crowded spaces.
The value of a reversing camera.
Perceived benefit for Powered Chair Users.
immediately before the intervention/procedure
Primary Post-trial Participant Evaluation of the possible Value of the Obstacle Alerting System Post-trial questionnaire based on pre-trial questionnaire. Participants reassessed the Obstacle Alerting System [OAS] in the light of experience.
In a face to face interview the participants were asked to score each question. 0=don't know, 1=not at all, to 5=very helpful. Participants were also asked to discuss the reasons for their choices.
Asked when they found the OAS helpful and when unhelpful. Assessment of the feedback options and when they were and were not helpful. How could the OAS be improved to make it more user friendly and environment specific.
Perceived benefit for Powered Chair Users.
immediately after the intervention/procedure
Primary Joystick range of movement patterns with and without the Obstacle alerting System Active Range of movement scatter plots/ heat maps immediately after the intervention/procedure
Primary Smoothness of joystick movement with and without the Obstacle alerting System Active Smoothness of movement e.g. Normalised Jerk Score. A lower score indicates smoother and more controlled movements.
Typical values for this trial are in the range of 3000-5000. A lower score is an indication of the participant learning to drive and becoming more familiar with the course.
A lower score may occur with the Obstacle Alerting system active - if it helps. A higher score if it distracts. At present this is a novel measure of these factors
immediately after the intervention/procedure
Primary Joystick path length with and without the Obstacle alerting System Active Joystick path length - distance the participant moves the joystick to drive the course. Calculated from the joystick displacement X and Y coordinates.
For a set course it would be expected that the path length will decrease as the participant learns to drive and familiarises with the course. Fatigue not having an impact.
A lower score may occur with the Obstacle Alerting system active - if it helps. A higher score if it distracts. At present this is a novel measure of these factors
immediately after the intervention/procedure
Primary Time to complete the course with and without the Obstacle alerting System Active Manually timed. Start when participant enters the course, stop when exiting the course immediately after the intervention/procedure
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