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Clinical effectiveness of wearable respiratory device for risk factor management of cerebrovascular disease

Clinical effectiveness of wearable respiratory device for risk factor management of cerebrovascular disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008133
Enrollment
100
Registered
2023-01-17
Start date
2023-03-28
Completion date
Unknown
Last updated
2024-08-19

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 : Clinical validity verification by comparing sleep stage classification results from polysomnography and sleep stage classification results from wearable breathing measuring devices

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Men and women aged 20 years or older who visited the hospital for diagnosis and treatment of cardiovascular disease, who understood the participation in the study and gave written consent to it

Exclusion criteria

Exclusion criteria: 1) Those with existing serious psychiatric disorders such as major schizophrenia and bipolar disorder 2) Those with untreated serious medical or surgical diseases 3) Those who are judged inappropriate to participate in this clinical trial according to the judgment of other researchers

Design outcomes

Primary

MeasureTime frame
Snoring and breathing rate during sleep, number and duration of snoring/apnea/hypopnea events

Secondary

MeasureTime frame
classification of REM sleep and sleep stages 3-4

Countries

Korea, Republic of

Contacts

Public Contacthyungoo kang

Jeonbuk National University Hospital

hgkang@jbnu.ac.kr+82-63-250-1590

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026