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Clinical Trials/NCT07397767
NCT07397767
Active, not recruiting
Not Applicable

Development of Quantitative Parameter of Upper Extremity Function in Patients With Brain Disorder Using Smart-Board and Smart-Glove, Single-Center, Prospective Study

Samsung Medical Center1 site in 1 country150 target enrollmentStarted: February 7, 2024Last updated:
Interventionssmart device

Overview

Phase
Not Applicable
Status
Active, not recruiting
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

Experimental

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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Won Hyuk Chang

Professor

Samsung Medical Center

Study Sites (1)

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