NCT07882810Not yet recruiting
Haptic-Assisted Virtual Reality Upper-Limb Rehabilitation After Intracerebral Haemorrhage
Feasibility and Preliminary Efficacy of Haptic-Assisted Virtual Reality Rehabilitation for Upper-Limb Motor Impairment After Spontaneous Intracerebral Haemorrhage: An Exploratory Substudy of the CrossReg-4-Health Cohort
Source: ClinicalTrials.gov · Last updated 20 Oct 2026
Brief summary (registry, in English)
After spontaneous intracerebral haemorrhage (ICH), many survivors have persistent weakness of the arm and hand. Virtual reality (VR) training with haptic (force-feedback) devices may support upper-limb recovery, but evidence comes mainly from ischaemic or mixed stroke populations. This exploratory substudy of the CrossReg-4-Health cohort will include 100 adults with upper-limb motor impairment after ICH. All participants will receive conventional physiotherapy and occupational therapy (ten 60-minute sessions over two weeks). Half will additionally receive 15 minutes of supervised haptic-assisted VR training per session using the Bimeo PRO system. Upper-limb motor function, disability, adherence, tolerability and adverse events will be assessed before and after the two-week programme to estimate feasibility and preliminary effect sizes for future trials.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 12 Oct 2026
- Start date
- 1 Nov 2026
- Primary completion date
- 30 Apr 2028
- Lead sponsor
- University Medical Centre Maribor
- Diseases
- Stroke
- NCT number
- NCT07882810
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 1 Nov 2026 to the primary completion date, 30 Apr 2028
- 3 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
- Intracerebral haemorrhage secondary to head trauma, intracranial neoplasm, isolated subarachnoid haemorrhage or another primary type of intracranial haemorrhage
Other
- End-of-life care decision
- Withdrawal of consent or major protocol violation
Who the study is looking for
- Participant in the CrossReg-4-Health cohort (age 18 years or older, acute spontaneous non-traumatic intracerebral haemorrhage confirmed by non-contrast CT or MRI)
- Residual upper-limb motor impairment
- Clinical stability
- Ability to participate safely in exercise
- Written informed consent for the substudy from the patient or a legally authorised representative
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| LKH-Universitätsklinikum Graz, Medical University of Graz Coordinator of this site? Confirm its status | Graz | Austria | Unknown status |
| Klinikum Klagenfurt am Worthersee Coordinator of this site? Confirm its status | Klagenfurt | Austria | Unknown status |
| University Medical Centre Maribor, Department of Neurology Coordinator of this site? Confirm its status | Maribor | Slovenia | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.