Development of Quantitative Parameter of Upper Extremity Function in Patients With Brain Disorder Using Smart-Board and Smart-Glove, Single-Center, Prospective Study
Overview
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Samsung Medical Center
- Enrollment
- 150
- Locations
- 1
- Primary Endpoint
- validity
Overview
Brief Summary
The aim of this study is to develop a novel quantitative metric for assessing upper-limb function in patients with neurological disorders. This will be accomplished by analyzing performance data obtained from a smart board and smart glove system and comparing these data with conventional clinical assessment methods currently used to evaluate upper-limb impairment.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Sequential
- Primary Purpose
- Diagnostic
- Masking
- None
Eligibility Criteria
- Ages
- 19 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adults aged 19 years or older.
- •Patients with upper-limb functional impairment due to neurological conditions such as stroke, cerebral palsy, brain tumor, traumatic brain injury, or Parkinson's disease.
Exclusion Criteria
- •Patients with progressive neurological disorders or those in a state of hemodynamic instability.
- •Patients with severe cognitive impairment (MMSE \< 10) or significant communication difficulty due to language disorders.
- •Any other condition in which the investigator determines that participation in the study is inappropriate.
Arms & Interventions
Smart Device User
Smart Device User
Intervention: smart device (Device)
Outcomes
Primary Outcomes
validity
Time Frame: the day of the study procedures
To examine the correlation between the primary outcome measure (FM-UE) and the trunk rehabilitation assessment model derived from mobile camera, smart board, and smart glove data.
Secondary Outcomes
No secondary outcomes reported
Investigators
Won Hyuk Chang
Professor
Samsung Medical Center