Active exploration of simulated textures to aid recovery after stroke
Official title: Research on the Effectiveness of the Method of Active Examination of Artificially Simulated Textures Generated by Programmable Transcutaneous Electrical Stimulation as a Method of Restoring Sensorimotor Function of the Upper Limbs
Run by Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health · NCT06962397 · Data updated 2026-11-12
This study tests a new sensory training method using virtual textures to see if it helps stroke survivors improve their arm and hand function better than standard rehab.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health Academic / other |
| Locations | 1 site (Moscow) |
| Status | Recruiting |
| Started | October 8, 2024 |
| Main results expected | June 1, 2025 |
| Study ends | January 2026 |
| Registry record updated | May 22, 2025 |
| Trial ID | NCT06962397 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18-80 who are more than one month post-stroke with a MoCA score of 20 or higher and a Barthel Index score of 3 or more.
✕Probably not a fit
Patients with severe upper limb paresis or significant depressive symptoms may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the effectiveness of a novel sensory rehabilitation method for stroke survivors experiencing upper limb sensorimotor impairments. Participants aged 18-80, more than one month post-stroke, will be divided into two groups: one receiving standard rehabilitation and the other undergoing active sensory training with programmable electrical stimulation that simulates virtual textures. The study aims to assess improvements in sensory function through various standardized tests before and after the intervention. By combining tactile exploration with real-time feedback, the trial seeks to enhance patient engagement and recovery outcomes.
Why it matters
Potential benefit: If successful, this approach could significantly improve sensory function and quality of life for stroke survivors.
How similar studies have gone: While traditional sensory rehabilitation methods have shown promise, this novel approach using programmable electrical stimulation is relatively untested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Episode of stroke confirmed by neuroimaging * More than one month post-stroke * Montreal Cognitive Assessment (MoCA) score ≥ 20 * Barthel Index score ≥ 3 * Ability to understand and follow instructions * Informed consent for participation and data collection * Age 18-80 years Exclusion Criteria: * Presence of depressive symptoms (HADS-Depression \> 11) * Upper limb paresis score below 35 on the Fugl-Meyer scale * Sensory impairment score below 3 or above 10 on the Fugl-Meyer scale
Where it's running
-
Federal Center of Cerebrovascular Pathology and Stroke
Moscow, Russia Recruiting
Study contacts
- Study coordinator: Maria Volodina, PhD in Physiology
- Email: mariavolodina@yandex.ru
- Phone: +79162528715
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.