Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT07156955

Proprioceptive Error Correction for Post-Stroke Upper Limb Rehabilitation

Led by Sungkyunkwan University · Updated on 2025-10-06

3

Participants Needed

1

Research Sites

45 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators aim to develop sensory transformation and augmentation technologies that minimize the impact of proprioceptive errors, thereby significantly enhancing motor learning and rehabilitation of the upper limbs. This study is designed to test proprioceptive error compensation techniques in stroke patients. The human nervous system often receives mismatched information from vision and proprioception during upper limb control, resulting in conflicting sensory inputs that limit the effectiveness of motor learning. In other words, real-time sensory feedback - a critical component of motor learning in the nervous system - is not reliably delivered. Therefore, this study seeks to resolve sensory conflicts by providing additional sensory information through electrical stimulation, with the goal of dramatically improving the effectiveness of motor learning.

CONDITIONS

Official Title

Proprioceptive Error Correction for Post-Stroke Upper Limb Rehabilitation

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with ischemic or hemorrhagic stroke
  • Stroke confirmed by CT or MRI
  • Stroke patients with proprioceptive sensory deficits
  • Chronic stroke with onset at least 3 months prior
  • Able to voluntarily flex and extend the elbow joint
  • Age 19 years or older
  • Provide written informed consent (participant or legal representative)
Not Eligible

You will not qualify if you...

  • Severe pain during elbow joint movement
  • Elbow joint contracture, spasticity, ataxia, musculoskeletal disorders, fractures, non-healing ulcers, or open wounds
  • Progressive or unstable stroke
  • Presence of unilateral neglect
  • Coexisting severe neurological disorders
  • Major psychiatric disorders such as major depressive disorder, schizophrenia, bipolar disorder, or dementia
  • Presence of a pacemaker

AI-Screening

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Trial Site Locations

Total: 1 location

1

Shinchon Severance Rehabilitation Hospital

Seoul, Seoul, South Korea, 03722

Actively Recruiting

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Research Team

J

June Seung Lee, Graduate student

CONTACT

H

Hyunhee Lim

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

6

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