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A Single-Center, Randomized, Prospective, Investigator-Initiated Exploratory Clinical Trial to Evaluate the Efficacy of Rehabilitation Training Using the Rehabilitation Robot (rebless planar) on Cognitive Function in Stroke Patients with Mild Cognitive Impairment and Hemiparesis

A Single-Center, Randomized, Prospective, Investigator-Initiated Exploratory Clinical Trial to Evaluate the Efficacy of Rehabilitation Training Using the Rehabilitation Robot (rebless planar) on Cognitive Function in Stroke Patients with Mild Cognitive Impairment and Hemiparesis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010564
Enrollment
34
Registered
2025-05-29
Start date
2025-08-12
Completion date
Unknown
Last updated
2026-04-27

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 : Randomized Controlled Trial, 2 Groups, 34 Participants 1. Experimental group: 30-minute cognitive rehabilitation training using the advanced rehabilitation exercise program of the reb

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Stroke patients aged 19 years or older 2. Patients with hemiparesis 3. Individuals with upper extremity spasticity scored 3 or less on the Modified Ashworth Scale 4. Individuals with an elbow Manual Muscle Test score of 2 or higher 5. Individuals with a Korean Mini-Mental State Examination score of 26 or lower

Exclusion criteria

Exclusion criteria: 1. Patients with severe communication difficulties due to cognitive impairment or aphasia 2. Patients with serious internal medical conditions that may interfere with training 3. Patients with neurological or musculoskeletal disorders that may affect training participation 4. Patients otherwise unable to perform upper extremity rehabilitation training 5. Patients who participated in another medical device study for the same indication (stroke) and are within 30 days of the completion visit 6. Patients deemed by the investigator to have severe cognitive impairment making participation in this clinical study difficult

Design outcomes

Primary

MeasureTime frame
Korean Mini-Mental State Examination (K-MMSE);Korean-Montreal Cognitive Assessment (K-MoCA)

Secondary

MeasureTime frame
Consortium to Establish a Registry for Alzheimer’s Disease (CERAD-K);Fugl-Meyer Assessment of the Upper Extremity (FMA-UE);Modified Barthel Index (MBI)

Countries

Korea, Republic of

Contacts

Public ContactMin Ho Chun

Asan Medical Center

mhchun0@gmail.com+82-2-3010-3796

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Aug 15, 2026