A multicenter confirmation clinical trial of untact upper extremity rehabilitation using smart board for late subacute and chronic patients with brain disorde

A multicenter confirmation clinical trial of untact upper extremity rehabilitation using smart board for late subacute and chronic patients with brain disorder - a randomized single-blinded controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010354

Enrollment

Registered

2025-03-28

Start date

2025-03-17

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : [Experimental group] -home-based upper limb rehabilitation training using the Neofect Smart board -a total of 20 sessions of home-based upper limb rehabilitation training using the Sm

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -Patients with neurological diseases aged 19 to 85 years old -Patients with hemiparesis lasting for more than 3 months due to neurological diseases (stroke, traumatic brain injury, brain tumor) and impaired upper limb function -Patients with shoulder flexor and adductor muscle strength of MRC grade 2 or higher -Patients with shoulder extensor and abductor spasticity of MAS grade 1+ or lower -Participants with sufficient cognitive function to understand the instructions from the researcher and the smart board, and to perform the tasks (K-MMSE =21)

Exclusion criteria

Exclusion criteria: -pre-existing significant neurogenic disorders -major psychiatric disorders such as schizophrenia, bipolar disorder, or dementia -History of diseases that caused pain or muscle atrophy in the affected upper limb before the onset of the neurological disease, which interfered with rehabilitation -Severe spasticity of the affected upper limb (Modified Ashworth Scale score =3) -skin disorders or open wounds on the affected upper limb -Amputation, fractures, or soft tissue-related diseases or injuries on the affected upper limb -severe pain that interferes with rehabilitation of the affected upper limb (Numeric Rating Scale > 6) -Inability to maintain a seated posture for more than 10 minutes, which is required for using the smart board -Significant visual impairment to the extent that the screen cannot be recognized when using the smart board

Design outcomes

Primary

Measure	Time frame
Fugl Meyer assessment scale	—

Secondary

Measure	Time frame
Action research arm test;Medical Research Council scale of muscle strength;Active Range of Motion ;Modified Ashworth Scale	—

Countries

Korea, Republic of

Contacts

Public ContactWon Hyuk Chang

Samsung Medical Center

wh.chang@samsung.com+82-2-3410-6068

Outcome results