Promoting BEST (BEtter, Faster, Longer, STronger) Walking for People With Parkinson's

NCT ID: NCT05801926

Last Updated: 2023-04-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-01-31
• Study Completion Date: 2024-01-31

Brief Summary

This project aims to improve how people with Parkinson's Disease (PD) walk. The global aim is to identify obstacles and solutions for people with PD for adopting technology to track and improve their gait to make them better and safer walkers. To meet this aim members of Parkinson Quebec will be surveyed about their technology readiness, physical, cognitive, and psychological health, and rehabilitation access. The survey should not take more than 20 minutes to complete on the web. Subsequently, a random sample of 100 survey participants will be offered a wearable device, the Heel2ToeTM sensor, designed to improve gait quality. This device emits a beep when a proper step is taken. This external cue reinforces the adoption of an adequate gait. In addition to the device, participants will be offered 5 sessions of telemonitoring to help them use the device optimally. Monitoring of use and outcomes will be over 3 months and the sensor is theirs to keep.

Detailed Description

The global aim of this research program is to identify technical, attitudinal, and motivational obstacles and solutions for people with PD for adopting technology to improve gait and to quantify changes in gait biomechanics that will make participants better and safer walkers, ultimately improving physical function, physical activity, motivation, and quality of life.

Specific objective: Among members of the PQ who meet the criteria for technology readiness and have sufficient walking capacity to use the Heel2ToeTM sensor at home, the objectives are to estimate the extent to which they: (1) require support from the technology and rehabilitation team to optimize use; (2) use the sensor; (3) and change gait pattern, walking behaviours, motivation and functional and quality of life indicators over a period of 3 months.

Design: An individualized, blocked, stepped-wedge design will be used, a design favoured for implementation science questions 63,64 and applicable here as the team does not have the resources to implement the technology to all participants all at once. Parkinson Quebec has provided funds to provide sensors for 100 people. Variable size clusters of people will be formed and randomized to receive the Heel2Toe sensor, training, and remote supervised use, at intervals of 3 weeks. The cluster size will be randomly determined ranging from 4 to 10. As everyone selected for the implementation have already filled out the survey, there is a common data set at project entry. This assessment will be repeated prior to being entered into the Heel2Toe phase and then 3 months later.

Conditions

Parkinson Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Immediate assignment

Within this block, half are assigned to receive the sensor right away.

Group Type: EXPERIMENTAL

Heel2Toe[TM] sensor

Intervention Type: DEVICE

Heel2Toe is a new generation of wearables that provides real-time auditory feedback when the person takes a good step, one in which the step is initiated with a strong heel strike.

Delayed assignment

Within this block, half are assigned to receive the sensor after a delay of 3 to 4 weeks

Group Type: ACTIVE_COMPARATOR

Heel2Toe[TM] sensor

Intervention Type: DEVICE

Heel2Toe is a new generation of wearables that provides real-time auditory feedback when the person takes a good step, one in which the step is initiated with a strong heel strike.

Interventions

Heel2Toe[TM] sensor

Heel2Toe is a new generation of wearables that provides real-time auditory feedback when the person takes a good step, one in which the step is initiated with a strong heel strike.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

Technology readiness will be determined by the following criteria:

• has wifi
• has a smartphone that is recent enough to support the technology or willing to acquire one
• uses apps on the smartphone on most days of the week with or without the aid of another person
• positively endorses the question "Are you interested in learning new things?"58 and "I walk outdoors on most days, weather permitting."

To screen participants for their capacity to use the Heel2Toe sensor, participants meeting the technology readiness criteria will be instructed to send a smartphone video of themselves doing a modified Timed-up-an-Go test65 in which the person, stands up from a chair, walks minimum of 10 meters (original TUG is 3 m.), turns, walks back to the chair, and sits down (long-TUG).

Exclusion Criteria

• unable to do the long TUG without assistance or need for a walking aid
• unable to recover balance independently from a perturbation during execution of the long TUG
• unable to reinitiate movement without assistance or without losing balance during a freezing event occurring during the long TUG. -

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MedTeq

INDUSTRY

Sponsor Role: collaborator

Healthy Brains for Healthy Lives

UNKNOWN

Sponsor Role: collaborator

Mitacs

INDUSTRY

Sponsor Role: collaborator

PhysioBiometrics Inc.

UNKNOWN

Sponsor Role: collaborator

Nancy Mayo

OTHER

Sponsor Role: lead

Responsible Party

Nancy Mayo

James McGill Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Division of Clinical Epidemiology

Montreal, Quebec, Canada

Research Institute of the McGill University Health Center, CORE, 5252 de Maisonneuve

Montreal, Quebec, Canada

Countries

Canada

Other Identifiers

A00-B37-22A / eRAP 22-04-037

Identifier Type: -

Identifier Source: org_study_id