Obstructive sleep apnea (OSA)
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who agree with this study
Exclusion criteria
Exclusion criteria: # Patients who are suspected to have other sleep related breathing disorders except for OSA and scheduled to undergo PSG # Patients have difficulty with wearing measuring equipment due to dementia, physically handicapped, and so on # Patients who is considered as unfit by a main researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The association among sleep disturbance focusing on sleep related breathing disorders at home, daily activity and parameters of lifestyle disease | — |
Secondary
| Measure | Time frame |
|---|---|
| To validate the measurement of sleep duration by Actiwatch 2 compared with PSG according to severity of sleep related breathing disorders. To validate that UW-301BT can measure sleep disturbance including sleep duration and daily activity, compared with Actiwatch 2 and Lifecorder. To explore the association among following items, OSA severity, sleep duration and daily activity 1) 3%ODI measured by Pulsox and Actiwatch 2 or UW-301BT 2) Sleep disturbance and activity measured by Actiwatch 2 and UW-301BT 3) Physical activity measured by Lifecorder and UW-301BT 4) Body weight and body composition 5) Sleep quality 6) Questionaires 7) Laboratory tests and urinalysis 8) Arterial blood gases 9) Visceral fat 10) Electrocardiography 11) Lung function test 12) Chest X ray 13) Vascular endothelial function measured by Endo-PAT | — |
Countries
Japan
Contacts
Graduate school of medicine, Kyoto University Respiratory medicine