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Recovery of Motor Skills With the Use of Artificial Intelligence and Computer Vision

NCT06183970 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-12-28

No results posted yet for this study

Summary

To investigate the impact of algorithms utilizing artificial intelligence technology and computer vision on the recovery of motor functions within the context of rehabilitation practice for patients who have experienced a cerebral stroke.

Conditions

  • Stroke
  • Hemiparesis
  • Spasticity as Sequela of Stroke
  • Dysmetria

Interventions

DEVICE

AssistI patients

The AsistI software package rehabilitation involves tailored upper limb exercises under an individual program. The regimen consists of 10-12 sessions, each lasting 30 minutes. Patients execute 10 exercises sequentially with their unaffected and affected limbs, involving tasks like touching mouth, forehead, and trunk parts with hand's brush, and amplitude movements in upper limb joints. AsistI assesses exercise accuracy, prevents unfavorable patterns, and logs target achievement, considering speed, accuracy, and repetitions.

DEVICE

Habilect patients

The Habilect rehab program involves 10-12 sessions using software and hardware. Patients perform upper limb exercises for 30 minutes individually, focusing on specific movements. They repeat 10 exercises, first with the healthy limb, then the affected one. Tasks include touching mouth, forehead, and trunk, along with joint movements like shoulder flexion. Habilect assesses exercise accuracy, preventing wrong moves, and tracks progress, considering speed, accuracy, repetitions.

Sponsors & Collaborators

  • Moscow Technical University of Communications and Informatics

    collaborator UNKNOWN

  • Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health

    lead OTHER

Principal Investigators

  • Michael Gorodnichev · Moscow Technical University of Communication and Informatics (MTUCI)

  • Galina Ivanova, Prof · Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-29
Primary Completion
2024-08-31
Completion
2025-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06183970 on ClinicalTrials.gov