Brain Disorder, Smart Device Rehabilitation
Conditions
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.
Interventions
DEVICEsmart device
Participants will undergo two sessions of upper-limb movement assessment using the smart board and smart glove on the day of the clinical trial. Simultaneously, video recordings will be obtained using a mobile camera. These procedures will be used to collect quantitative data on upper-limb movements.
Sponsors
Samsung Medical Center
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| validity | 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. |
Countries
South Korea
Outcome results
None listed