Digital Interactive Technologies in Rehabilitation of Post-sroke Patients With Impaired Fine Function of the Hand
Launched by MOSCOW SCIENTIFIC AND PRACTICAL CENTER OF MEDICAL REHABILITATION, RESTORATIVE AND SPORTS MEDICINE · Jan 27, 2022
Trial Information
Current as of August 11, 2025
Unknown status
Keywords
ClinConnect Summary
The study is an open-label observational trial. Brain stroke (BS) is one of the main causes of upper limb (UL) dysfunction and limitations of daily human activity.The fine use of the hand imparement is often combined with speech, cognitive and emotional disturbances, which is due to the anatomical proximity and close functional relationships of the corresponding areas in the cerebral cortex.
The objective of the present study will be to evaluate the effectiveness and safety of the digital interactive technology (DIT) with artificial intelligence and biofeedback Smart glove "SensoRehab" (SG...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Men or women aged 18 to 70 years after a first-onset IS, early (1-6 months), late recovery (6-12 months) periods.
- • 2. Supratentorial IS according to MRI of the brain.
- • 3. The severity of UL paresis ranged from a score of 4 to 3 according to the Medical Research Council Scale (MRCS).20
- • 4. Spasticity of 2 points or less by the Modified Ashworth Scale (MAS)
- • 5. Cognitive function more than 20 points on the Montreal Cognitive Assessment (MoCA)
- • 6. Affective disorders score less than 11 on the Hospital Anxiety and Depression Scale (HADS)
- • 7. The patient's ability and willingness to comply with the requirements of this protocol.
- Exclusion Criteria:
- • 1. Concomitant neurological diseases causing decreased muscle strength or increased muscle tone in the UL (e.g., cerebral palsy, brain injury).
- • 2. Clinically significant limitation of the passive movement amplitude in the joints of the investigated hand, pronounced contracture and deformities of the upper extremity.
- • 3. Use of other DIT, BFB techniques to restore impaired UL function within 30 days prior to the patient Inclusion Visit.
- • 4. Severe visual impairment, decreased visual acuity of less than 0.2 in the worst eye according to the Golovin-Sivtsev Table24.
- • 5. Sensory aphasia, gross motor aphasia.
- • 6. Recurrent stroke.
- • 7. Unstable angina and/or heart attack in previous month.
- • 8. Uncontrolled arterial hypertension.
- • 9. Somatic diseases in decompensation stage.
- • 10. Alcohol abuse, medical marijuana use or soft drug abuse within the 12 months prior to the Inclusion Visit.
- • 11. Any medical condition, including mental disease or epilepsy that could affect the interpretation of study results, the study procedures or patient safety.
- • 12. Pregnancy.
- • 13. Lactation.
About Moscow Scientific And Practical Center Of Medical Rehabilitation, Restorative And Sports Medicine
The Moscow Scientific and Practical Center of Medical Rehabilitation, Restorative and Sports Medicine is a leading institution dedicated to advancing the fields of medical rehabilitation and sports medicine through innovative research and clinical trials. With a commitment to improving patient outcomes and enhancing recovery processes, the Center combines scientific expertise with practical applications, focusing on evidence-based practices and interdisciplinary approaches. Its collaborative efforts aim to develop and implement cutting-edge rehabilitation techniques, ultimately contributing to the enhancement of physical health and performance in various populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Moscow, , Russian Federation
Patients applied
Trial Officials
Elena V Kostenko, MD
Principal Investigator
Moscow Scientific and Practical Center of Medical Rehabilitation, Restorative and Sports Medicine
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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