Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06962397

Effectiveness of Active Exploration of Simulated Textures for Sensorimotor Recovery

Led by Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health · Updated on 2025-05-22

20

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Effectiveness of Active Exploration of Simulated Textures for Sensorimotor Recovery

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Federal Center of Cerebrovascular Pathology and Stroke

Moscow, Russia, 117997

Actively Recruiting

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Research Team

M

Maria Volodina, PhD in Physiology

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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