Biometric Data Usage for Intensity Control of Robotic Rehabilitation on Stroke Patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005827

Enrollment

Registered

2021-01-27

Start date

2018-10-25

Completion date

Unknown

Last updated

2021-02-23

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 : This study were randomly assigned to one of two groups in a 1:1 ratio. The random assignment was performed by using a random number table. On first group, the rehabilitation intensit

s subjective judgement. The second group adjust intensity based on bio-metric data. Robotic rehabilitation will be for 20 minutes five times a week for 3 weeks.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: A. who are over 19 year old B. who have gait disturbance or hemiplegia after primary stroke C. who are admitted to rehabilitation department and got rehabilitation therapy

Exclusion criteria

Exclusion criteria: A. who are not able to control neck B. who have cognitive impairment, in which cannot follow 1 step command C. vital sign is unstable, and need emergency treatment D. who are taking Beta blocker

Design outcomes

Primary

Measure	Time frame
functional ambulation category(FAC) Modified barthel index (MBI) Berg balance scale(BBS) Timed Up and Go test(TUG) 10 meter walk test (10MWT)	—

Secondary

Measure	Time frame
Biometric data: EKG, heart rate, blood pressure, respiratory rate	—

Countries

Korea, Republic of

Contacts

Public ContactJiae Kim

Asan Medical Center

Outcome results