Feasibility of home-based pressure monitoring using smartwatch in patients with Parkinson’s dis ease and atypical parkinsonism

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006786

Enrollment

Registered

2021-11-26

Start date

2021-12-01

Completion date

Unknown

Last updated

2021-12-02

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 : Measurement of the blood pressure for 4 weeks regular based and when participants feel symptoms related with orthostatic hypotension using the Smartwatch.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Parkinson's disease patients based on the international Parkinson’s disease and Movement Disorders Society Criteria Idiopathic Parkinson’s disease 2. Atypical parkinsonism patients based on the Diagnostic criteria for progressive supranuclear palsy and second consensus for diagnosis of multiple system atrophy

Exclusion criteria

Exclusion criteria: Patients with 1. Unable to measure of blood pressure because of arrhythmia, cardiovascular disease 2. Unable to measure of blood pressure because of musculoskeletal disease patients 3. Patients with a difference of 10 mmHg or more in systolic blood pressure between upper arms 4. Unable to measure of blood pressure because of severe resting tremor or dyskinesia 5. Other patients who deemed inappropriate for the study by the researcher 6. demented patients based on DSM-V

Design outcomes

Primary

Measure	Time frame
Feasibility of home-based blood pressure measured by smartwatch	—

Secondary

Measure	Time frame
Association between the measured blood pressure and orthostatic symptoms	—

Countries

Korea, Republic of

Contacts

Public ContactJong Hyeon Ahn

Samsung Medical Center

jhahn0513@gmail.com+82-2-3410-0893

Outcome results