Actively Recruiting
Feasibility and Cost of Robot-assisted Upper Limb Rehabilitation with Different Levels of Supervision
Led by Swiss Federal Institute of Technology · Updated on 2025-03-06
100
Participants Needed
2
Research Sites
303 weeks
Total Duration
On this page
Sponsors
S
Swiss Federal Institute of Technology
Lead Sponsor
C
Clinica Hildebrand Brissago
Collaborating Sponsor
AI-Summary
What this Trial Is About
Upper limb impairments are often a result of neurological or traumatic injuries (e.g., stroke, traumatic brain injuries). These impairments may decrease independence in performing activities of daily living, severely affecting patients' quality of life. Growing evidence shows that increasing upper limb therapy dose for patients could improve functional outcomes and prevent their long-term deterioration. However, due to limited resources (e.g., the number of therapists) and high rehabilitation-related costs, providing a higher therapy dose to patients is challenging, both in the clinic and after discharge, and finding new models of care is therefore critical. Minimally supervised or unsupervised robot-assisted therapy (i.e., patients training with rehabilitation devices with minimal to no supervision of an external person) holds the promise of allowing an increase in therapy dose with little impact on the additional resources needed. Because of their ability to provide active support and measure a wide set of parameters, actuated (active) rehabilitation robots seem to be the best solution for this therapy setting. However, such devices are often complex to use and have never been extensively tested minimally or unsupervised. Consequently, the data available on their feasibility and cost-effectiveness is limited. At the Rehabilitation Engineering Laboratory (RELab, ETH Zurich), we developed ReHandyBot, an actuated device for unsupervised upper limb therapy. The device has already been tested with stroke patients in an unsupervised setting, with positive results regarding usability and increase in therapy dose. The main goal of this project is, therefore, to investigate the feasibility and cost of our robot-assisted continuum of care model (i.e., from inpatient to ambulatory). Specifically, we aim to evaluate the feasibility of integrating ReHandyBot into the clinical routine and perform a preliminary cost-benefit analysis of supervised, minimally supervised, and unsupervised robot-assisted therapy. Furthermore, we will also gather data on the overall dose of robot-assisted therapy and the intensity of use of the device in a clinical and ambulatory setting.
CONDITIONS
Official Title
Feasibility and Cost of Robot-assisted Upper Limb Rehabilitation with Different Levels of Supervision
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent from the participant
- Male or female patients aged 18 to 90 years
- Presence of an upper limb deficit from any condition that could benefit from ReHandyBot therapy as determined by clinicians
You will not qualify if you...
- Any medical condition that may interfere with training using the ReHandyBot device
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Clinica Hildebrand Centro di riabilitazione Brissago
Brissago, Switzerland, 6614
Actively Recruiting
2
Clinica Hildebrand Centro Ambulatoriale Lugano
Lugano, Switzerland
Actively Recruiting
Research Team
G
Giada Devittori, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here