NCT07270484Completed
Rehabilitation Based on Hybrid Neuroprosthesis
Rehabilitation Based on Hybrid Neuroprosthesis: Evaluation of the Feasibility, Functionality and Usability of the System in a Post-stroke Patient Population.
Source: ClinicalTrials.gov · Last updated 22 Dec 2025
Brief summary (registry, in English)
The study is a pilot, multi-center, prospective, and open study to test feasibility, functionality and usability of a device defined as a hybrid neuroprosthesis.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 24 (actual)
- First submitted
- 12 Sept 2025
- Start date
- 12 Feb 2024
- Primary completion date
- 24 May 2024
- Lead sponsor
- Villa Beretta Rehabilitation Center
- Diseases
- Stroke
- NCT number
- NCT07270484
What you commit to
- Study type: Interventional
- Participants enrolled: 24
- From 12 Feb 2024 to the primary completion date, 24 May 2024
- 2 sites in 2 countries
- 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
- Severe psychiatric disorder
- Permanent neurological symptoms present immediately before stroke
- Physical conditions that can alter normal biomechanics (e.g., recent sprains or injuries, etc.)
- Unstable medical condition
Other
- Subjects with a high level of spasticity (Modified Ashworth Scale: In general \>3 except for motorized joints which may be \>2)
- Pain in the affected upper limb (Numeric Rating Scale \> 4)
- Pregnant or nursing women
- No written informed consent from the patient or the legal representative
- Active implantable devices (e.g., pacemaker)
Who the study is looking for
- Adults (women or men aged ≥ 18 years)
- with a diagnosis of stroke either hemorrhagic or ischemic
- with a hemiparesis of the upper limb (0 ≤ MRC ≤ 4)
- in sub-acute (up to six months after acute event) or chronic condition (more than 6 months from the acute event).
- Able to sit upright for the duration of the test.
- Subjects with a level of cognitive capacity that enables him/her to follow the instructions related to the performance of exercises.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Schön Klinik Coordinator of this site? Confirm its status | Bad Aibling | Germany | Unknown status |
| Villa Beretta Rehabilitation Center Coordinator of this site? Confirm its status | Costa Masnaga | Italy | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.