About this trial
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.
Eligibility criteria
Qualifiers
Episode of stroke confirmed by neuroimaging
More than one month post-stroke
Montreal Cognitive Assessment (MoCA) score ≥ 20
Barthel Index score ≥ 3
Disqualifiers
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
Trial design
Treatments tested in this trial
- Active Touch-Based Sensory Training