Using virtual reality and neurostimulation to help stroke recovery
Virtual Reality (VR) Platform and Transcutaneous Electrical Nerve Stimulation (TENS) for Early Stroke Rehabilitation
NA · Medical University of Vienna · NCT06887231
This study is testing if using virtual reality and a special electrical stimulation can help stroke patients recover better by improving their movement and feeling.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 35 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Medical University of Vienna (other) |
| Locations | 1 site (Vienna, State of Vienna) |
| Trial ID | NCT06887231 on ClinicalTrials.gov |
What this trial studies
This study explores the use of virtual reality (VR) combined with transcutaneous electrical nerve stimulation (TENS) to enhance rehabilitation for stroke patients in the subacute phase. It aims to address both motor and sensory impairments that often hinder recovery by integrating multisensory feedback into the rehabilitation process. Participants will engage in task-oriented movements while receiving VR and TENS interventions, compared to conventional rehabilitation methods. The goal is to improve overall recovery outcomes by considering the role of sensory feedback and body perception.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 80 who have experienced an ischemic or hemorrhagic stroke and are in the subacute recovery phase.
Not a fit: Patients with other neurological conditions, severe cognitive impairments, or those experiencing virtual reality motion sickness may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance recovery and quality of life for stroke survivors by improving both motor and sensory functions.
How similar studies have performed: While the combination of VR and TENS is a novel approach, there is growing evidence supporting the effectiveness of VR in rehabilitation, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria:
* Confirmed diagnosis of ischemic or hemorrhagic stroke
* In the subacute phase (from 7 days to 3 months from last stroke onset)
* Fugl-Meyer-Upper Extremity (FMUE) scale for the motor part: FMUE ≥ 10
* Ability to sit in an upright position
* Age between 18 and 80 years
Exclusion Criteria:
* Other neurological or physical impairment or mental condition that, in the judgment of the investigator, does not allow participation in the study.
* Mini-Mental State Examination (MMSE) \< 24
* Epilepsy
* Nausea, headaches or fatigue due to VR-generated environment ("virtual reality motion sickness")
* Peripheral nerve damage in the affected arm or hand
* Pacemaker or other electronic implants
Where this trial is running
Vienna, State of Vienna
- Medical University of Vienna, Department of Neurology — Vienna, State of Vienna, Austria (RECRUITING)
Study contacts
- Study coordinator: Andrea Cimolato, PhD
- Email: andrea.cimolato@meduniwien.ac.at
- Phone: +4314040039224
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke, Virtual Reality, Transcutaneous Electrical Nerve Stimulation, Multisensory integration, Task oriented movement, Rehabilitation