NCT06962397Recruiting
Effectiveness of Active Exploration of Simulated Textures for Sensorimotor Recovery
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
Source: ClinicalTrials.gov · Last updated 22 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Parallel-group, single-blinded controlled clinical trial. The study includes people aged 18-80 years, more than one month after stroke, with confirmed diagnosis, MoCA ≥ 20, and Barthel Index ≥ 3. The control group receives standard rehabilitation. The experimental group also receives active sensory training with programmable electrical stimulation to simulate virtual textures. Sensory function was assessed before and after the training using standard tests, including Fugl-Meyer, ARAT, 9HPT, and monofilament testing.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 30 Apr 2025
- Start date
- 8 Oct 2024
- Primary completion date
- 1 Jun 2025
- Lead sponsor
- Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health
- Diseases
- Stroke
- NCT number
- NCT06962397
What you commit to
- Study type: Interventional
- Planned participants: 20
- From 8 Oct 2024 to the primary completion date, 1 Jun 2025
- 1 site in 1 country
- 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
- Sensory impairment score below 3 or above 10 on the Fugl-Meyer scale
Other
- Presence of depressive symptoms (HADS-Depression \> 11)
- Upper limb paresis score below 35 on the Fugl-Meyer scale
Who the study is looking for
- 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
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Federal Center of Cerebrovascular Pathology and Stroke Coordinator of this site? Confirm its status | Moscow | Russia | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.