NCT03394599

Brief Summary

Motiview, an activity healthcare solution by Motitech, is finding solutions for elderly and people with dementia by reducing unnecessary emergency department visits, preventing falls/fall-injuries, improving management of complex health conditions, and improving brain health/cognitive fitness. Motiview is based on the premise that many of the challenges faced by this population may be caused by inactivity. The solution needs to effectively motivate them to be active year round. It also needs to accomplish this without increasing the resources within the health system. Motiview stimulates elderly people and people with dementia to increase their physical activity and cognitive training. By using videos, music/sound, the user can take a virtual bicycle trip through familiar surroundings and memories while facilitating activity participation and adherence in the older adult. Motiview is coupled to a mobile user-adapted cycle-trainer (TheraTrainer) that elicits physical activity as the individual pedals the trip. The unique part is adapting films and music according to the users' wishes and memories. By lessening the perceptions of difficulty, monotony, and discomforts associated with physical activity, participation and the experience of physical activity is enhanced. The research protocol of this project is designed to document the added value of Motiview for achieving physical activity participation. The hypothesis being that TheraTrainer bicycles will provide more activity when used with the video/audio overlay. Qualitative data will be gathered on the social aspects and reminiscence observed with the video/audit overlay from clients, care givers and staff. Information about Motiview can also be found on the website at https://www.motitech.no/en

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2018

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 20, 2017

Completed
20 days until next milestone

First Posted

Study publicly available on registry

January 9, 2018

Completed
6 days until next milestone

Study Start

First participant enrolled

January 15, 2018

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2019

Completed
Last Updated

September 5, 2021

Status Verified

September 1, 2021

Enrollment Period

1.1 years

First QC Date

December 20, 2017

Last Update Submit

September 2, 2021

Conditions

Keywords

Physical ActivityRehabilitationExerciseEngagementOlder Adults

Outcome Measures

Primary Outcomes (1)

  • Psycho-social

    Micro-interviews after use of the TheraTrainer

    Through study completion, an average of 8 weeks.

Secondary Outcomes (1)

  • Qualitative Feedback

    One time, during the week following the intervention period.

Study Arms (2)

TheraTrainer Only

ACTIVE COMPARATOR

The 30 clients (15 per site) will have the opportunity to engage in cycling on the TheraTrainer only for the duration of their participation at the Geriatric program. Their carers will also be recruited.

Device: TheraTrainer Only

TheraTrainer + Motiview

EXPERIMENTAL

The 30 clients (15 per site) will have the opportunity to engage in cycling on the TheraTrainer with the addition of Motiview (engaging videos to watching while cycling). Their carers will also be recruited.

Device: TheraTrainer + Motiview

Interventions

TheraTrainer will be used in conjunction with Motiview.

TheraTrainer + Motiview

TheraTrainer will be used.

TheraTrainer Only

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Clients-
  • Will be attending the Geriatric Day Hospital program at Bruyere Continuing Care or the Day Treatment Centre at Baycrest Health Sciences
  • Able to provide informed consent
  • Able to safely use a TheraTrainer
  • Would be using the exercise cycle as part of regular therapy in the GDH (Bruyere only) as determined by their health care team.
  • Carer-
  • Able to provide informed consent.
  • Staff-
  • Employed at the Geriatric Day Hospital/Day Treatment Centre program at the time of client enrollment.

You may not qualify if:

  • Client-
  • Told by the therapists not to use the TheraTrainer as part of their rehabilitation.
  • Carer-
  • Staff-

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Bruyere Research Institute

Ottawa, Ontario, K1N 5C8, Canada

Location

Baycrest Health Sciences

Toronto, Ontario, M6A 2E1, Canada

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Heidi Sveistrup, PhD

    Bruyère Health Research Institute.

    PRINCIPAL INVESTIGATOR
  • Tim Pauley, MSc

    West Park

    PRINCIPAL INVESTIGATOR
  • Fidelma Serediuk, BSc PT, MSc

    Baycrest

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Interim CEO and Chief Scientific Officer of the Bruyère Research Institute and VP, Research and Academic Affairs

Study Record Dates

First Submitted

December 20, 2017

First Posted

January 9, 2018

Study Start

January 15, 2018

Primary Completion

February 28, 2019

Study Completion

February 28, 2019

Last Updated

September 5, 2021

Record last verified: 2021-09

Data Sharing

IPD Sharing
Will not share

All collected (de-identified) IPD will be shared between sites but not made accessible to other researchers.

Locations