Combining virtual reality and TENS for stroke rehabilitation
Multimodal Platform Combining VR and TENS for Stroke Rehabilitation
This study is testing whether using virtual reality along with electrical stimulation can help stroke survivors recover better than traditional rehab methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Institute Mihajlo Pupin Academic / other |
| Locations | 1 site (Belgrade) |
| Trial ID | NCT06400823 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of a multimodal rehabilitation approach that combines virtual reality (VR) and transcutaneous electrical nerve stimulation (TENS) for patients recovering from stroke. The intervention aims to enhance motor and sensory recovery by integrating sensory-motor training with electrical stimulation. Participants will be compared against those receiving conventional rehabilitation methods to assess improvements in upper-limb function and cognitive body representation. The study targets stroke survivors who are at least three months post-incident and have specific motor function scores.
Who should consider this trial
Good fit: Ideal candidates for this study are ischemic or hemorrhagic stroke patients who are at least three months post-stroke and have a specific range of motor function scores.
Not a fit: Patients with prior neurological or psychiatric disorders, severe cognitive impairment, or those with electronic implants may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve rehabilitation outcomes and functional independence for stroke survivors.
How similar studies have performed: While there is emerging evidence supporting the use of VR and TENS in rehabilitation, this specific multimodal approach is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ischemic or haemorrhagic stroke patient * At least 3 months after the stroke incident * 10 \<= FMUE \<= 60 (motor function) Exclusion Criteria: * Prior neurological or psychiatric disorders * Severe cognitive impairment (MoCA score \<10) * Epilepsy * Pacemakers or other electronic implants * Unable to give an informed consent form
Where this trial is running
Belgrade
- Clinic for rehabilitation dr Miroslav Zotovic — Belgrade, Serbia (Recruiting)
Study contacts
- Principal investigator: Stanisa Raspopovic, PhD — Mihajlo Pupin Institute
- Study coordinator: Natalija Secerovic, PhD
- Email: natalija.katic@pupin.rs
- Phone: +381631268862
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.