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Generalizability of Unsupervised Therapy After Stroke in the Home Setting With a Hand Rehabilitation Device (ReHandyBot)

Key facts

Where
Bellikon, Geneva, Valens, and Zihlschlacht, SwitzerlandSee the 4 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 90 years old?

Source: NCT07674238, who can take part

Where in Switzerland

  • Rehaklinik BellikonBellikon, SwitzerlandNo longer taking part
  • University Hospital GenevaGeneva, SwitzerlandNo longer taking part
  • Rehaklinik ValensValens, SwitzerlandNo longer taking part
  • Rehaklinik Zihlschlacht AGZihlschlacht, SwitzerlandNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Swiss Federal Institute of Technology
Trial code
NCT07674238
Record updated
21 September 2026
Original description
The ReHandyBot (RHB) is a robot for hand rehabilitation after stroke. The aims of this study are to investigate (i) the generalizability of unsupervised therapy with the ReHandyBot within patients' home after discharge from a clinic, (ii) compliance, as measured by the amount of unsupervised robot-assisted therapy dose (e.g., therapy time) performed by the subjects after discharge, (iii) the usability of ReHandyBot and user experience during robot-assisted therapy, and (iv) the effect of the increase in therapy dose achieved with our device compared to standard care. The study consists of two primary phases. The first is a familiarization phase conducted at the clinic, where therapists teach participants how to perform the exercises using the robot. Then, if capable of training with the robot safely, after discharge from the clinic, participants can bring the robot home and autonomously train with it. The hypothesis is that unsupervised therapy might be a possible way to increase therapy dose for stroke patients, with the potential to further improve recovery of hand function, with minimal additional burden for therapists and for the healthcare system.Read full original descriptionShow less

Generalizability of Unsupervised Therapy After Stroke in the Home Setting With a Hand Rehabilitation Device (ReHandyBot): a Multicentric, Exploratory Study

The ReHandyBot (RHB) is a robot for hand rehabilitation after stroke. The aims of this study are to investigate (i) the generalizability of unsupervised therapy with the ReHandyBot within patients' home after discharge from a clinic, (ii) compliance, as measured by the amount of unsupervised robot-assisted therapy dose (e.g., therapy time) performed by the subjects after discharge, (iii) the usability of ReHandyBot and user experience during robot-assisted therapy, and (iv) the effect of the increase in therapy dose achieved with our device compared to standard care. The study consists of two primary phases. The first is a familiarization phase conducted at the clinic, where therapists teach participants how to perform the exercises using the robot. Then, if capable of training with the robot safely, after discharge from the clinic, participants can bring the robot home and autonomously train with it. The hypothesis is that unsupervised therapy might be a possible way to increase therapy dose for stroke patients, with the potential to further improve recovery of hand function, with minimal additional burden for therapists and for the healthcare system.

Inclusion: Informed Consent signed by the subject; female and male patients between 18 and 90 years old; acute/subacute stroke (recruitment within 12 weeks from stroke onset); pre-stroke modified Rankin score ≤ 1; National Institutes of Health Stroke Scale (NIHSS) ≥ 1 in at least one of the items regarding motor functions, sensory functions and ataxia; possibility (e.g., enough space) to set up the ReHandyBot at home.

Exclusion: functional impairment of the upper limb due to other pathologies; modified Ashworth Scale > 2 for one or more of the following muscles: shoulder adductors, forearm pronator and supinator, flexors and extensors of elbow, wrist and fingers; moderate to severe aphasia: Goodglass-Kaplan's scale < 3; moderate to severe cognitive deficits: levels of cognitive functioning-revised (LCF-R) < 9; severe pain in the affected arm: visual analogue scale for pain (VASp) ≥ 5; other pathologies which may interfere with the study; after discharge the patient will go to an assisted living facility (e.g., care home).

ClinicalTrials.gov NCT07674238