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Usefulness and Acceptability of a Connected Ergocycle for the Elderly in a Clinical Setting

Usefulness and Acceptability of a Connected Ergocycle for the Elderly in a Clinical Setting

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05404633
Enrollment
20
Registered
2022-06-03
Start date
2021-08-31
Completion date
2023-05-31
Last updated
2023-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End-stage Renal Disease

Brief summary

Hospitalizations are harmful to patients. Without a proper intervention, it will lead to a permanent decline in physical function, especially among frail individuals. Ultimately, this will worsen quality of life, as well as the cognitive and functional status of affected elderly people, which will arguably reduce functional independence, increase post-discharge institutionalization and death among frail older adults. It is known that patients receiving early physical evaluation and rehabilitation (in the 24 hours following admission) improves post-discharge orientation, decreases delirium and the need of acute care. The rehabilitation often involves ergocycles, but commercially available devices are expensive and often hard to move, to set up in hospital bed and lack connectivity. In this context, a connected ergocycle prototype which has a number of desired characteristics, including low production cost, relatively light and easy to move and with internet connectivity. The goal of this study is thereby to assess the usefulness and acceptability of the prototype with health professionals involved in physical rehabilitation and patients receiving said rehabilitation.

Interventions

DEVICEErgogycle prototype testing for acceptability

The objective was to assess the acceptability of the ergogycle prototype (device) while used in a clinical settings by both the patients and the professionals.

Sponsors

Université de Sherbrooke
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

: * \> 55 years old * receiving treatments for terminal renal insufficiency at least 3 times a week, for at least 3 months (hemodialysis; HD) or under mechanical ventilation for less than 72 hours, and that should last for at least 24 more hours (intensive unit care; ICU) * Physically independent outside HD or before admission (ICU) (≥ 70 on the Barthel index) * with medical clearance (HD : nephrologist; ICU : intensivist)

Exclusion criteria

* unable to walk without assistance (before ICU admission) * diagnosed neurocognitive decline * recent hemiarthroplasty for a hip fracture that causes a limitation in the flexion of the hip during pedaling * already involved in another study

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the deviceup to 1 hour after the exercise session for both the patients and professionalsQuestionnaire based on the unified theory of acceptance and use of technology

Countries

Canada

Contacts

Primary ContactEléonor Riesco, PhD
eleonore.riesco@usherbrooke.ca1-819-821-8000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026