Evaluation of active posture correction method in upper limb rehabilitation robot training for stroke patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009739

Enrollment

Registered

2024-08-30

Start date

2024-08-19

Completion date

Unknown

Last updated

2025-01-06

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 : - To evaluate the patients upper extremity motor function, Fugl-Meyer Assessment of the Upper Extremity (FMA-UE), Modified Barthel Index (MBI), Modified Ashworth Scale (MAS), Range of

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients aged 19 years and older with stroke 2. Patients with unilateral paralysis(Hemiparesis) 3. Anyone with a Modified Ashworth Scale of 3 or less on the upper arm. 4. Anyone with a score of 2(Poor) or more on the Elbow Manual Muscle Test

Exclusion criteria

Exclusion criteria: 1. Patient with impairment of communication due to cognitive impairment or aphasia. 2. Patient with serious medical conditions that may affect training. 3. Patient with neurological or musculoskeletal disorders that may affect training. 4. Inability to perform other upper limb rehabilitation training 5. Patient participating in a medical device study with the same indication(stroke) as this study, within 30 days after the end of the visit.

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer Assessment of the Upper Extremity (FMA-UE)	—

Secondary

Measure	Time frame
Motricity Index (MI)_Upper;Modified Barthel Index (MBI);Range of Motion (ROM);Modified Ashworth Scale (MAS);Wolf Motor Function Test (WMFT)	—

Countries

Korea, Republic of

Contacts

Public ContactHyo Jin Jeon

Asan Medical Center

hyo4850@gamil.com+82-2-3010-8622

Outcome results