NCT07397767

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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
7mo left

Started Feb 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress79%
Feb 2024Dec 2026

Study Start

First participant enrolled

February 7, 2024

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 23, 2025

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

January 20, 2026

Completed
20 days until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Expected
Last Updated

February 9, 2026

Status Verified

February 1, 2026

Enrollment Period

1.9 years

First QC Date

January 20, 2026

Last Update Submit

February 5, 2026

Conditions

Brain DisorderSmart Device Rehabilitation

Outcome Measures

Primary Outcomes (1)

  • validity

    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.

    the day of the study procedures

Study Arms (1)

Smart Device User

EXPERIMENTAL

Smart Device User

Device: smart device

Interventions

smart deviceDEVICE

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.

Smart Device User

Eligibility Criteria

Age19 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Samsung Medical Center

Seoul, South Korea

Location

MeSH Terms

Conditions

Brain Diseases

Condition Hierarchy (Ancestors)

Central Nervous System DiseasesNervous System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 20, 2026

First Posted

February 9, 2026

Study Start

February 7, 2024

Primary Completion

December 23, 2025

Study Completion (Estimated)

December 31, 2026

Last Updated

February 9, 2026

Record last verified: 2026-02

Locations

KR(1)