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NCT07674238Not yet recruiting

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

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

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
16 Jun 2026
Start date
1 Nov 2026
Primary completion date
30 May 2028
Lead sponsor
Swiss Federal Institute of Technology
Diseases
Stroke
NCT number
NCT07674238

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Nov 2026 to the primary completion date, 30 May 2028
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • functional impairment of the upper limb due to other pathologies;

Other

  • 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).

Who the study is looking for

  • 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.

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Rehaklinik Bellikon
Coordinator of this site? Confirm its status
BellikonSwitzerlandUnknown status
University Hospital Geneva
Coordinator of this site? Confirm its status
GenevaSwitzerlandUnknown status
Rehaklinik Valens
Coordinator of this site? Confirm its status
ValensSwitzerlandUnknown status
Rehaklinik Zihlschlacht AG
Coordinator of this site? Confirm its status
ZihlschlachtSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.