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Establishment and application of home wireless remote diagnosis and treatment system for sleep respiratory diseases

Randomized controlled clinical trial on the effectiveness and cost-effectiveness of remote and routine outpatient care for patients with sleep apnea

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030546
Enrollment
Unknown
Registered
2020-03-06
Start date
2019-02-02
Completion date
Unknown
Last updated
2020-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep apnea syndrome

Interventions

telemedicine group:Patients were followed up by remote video follow-up
telemedicine group:The patients obtained the questionnaire link by email and filled in the questionnaire on the mobile or computer side

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Access in the home to the internet, e-mail, and phone on all days; 3. Living in Beijing so that participants randomized to in-person delivery of care will be able to travel to and from the sleep center; 4. Fluent in Chinese as assessed on the initial phone contact.

Exclusion criteria

Exclusion criteria: 1. Unable or unwilling to provide informed consent and complete required questionnaires; 2. Previous diagnosis of OSA, central sleep apnea (>=50% of apneas on diagnostic testing are central apneas), Cheyne-Stokes breathing, obesity hypoventilation syndrome, or narcolepsy; 3. Previous treatment with PAP, non-nasal surgery for OSA, or current use of supplemental oxygen; 4. A clinically unstable medical condition in the previous 2 months as defined by a new medical diagnosis (e.g., pneumonia, cardiac disease, thyroid disease, depression or psychosis, cirrhosis, cancer, etc.); 5. Individuals who regularly experience jet lag or irregular work schedules over the previous 3 months; 6. Women who are pregnant or women who are sexually active and of child-bearing age who are not using some form of contraceptive; 7. Unable to perform tests due to visual (inability to read the consent form) or hearing (unable to have a phone conversation) impairment, or unable to perform activities of daily living.

Design outcomes

Primary

MeasureTime frame
Height;weight;blood pressure;Neck circumference;Waist circumference;Hip circumference;Apnea hypopnea index;compliance;

Countries

China

Contacts

Public ContactHan Fang

Peking University People's Hospital

hanfang1@hotmail.com+86 010-88324207

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026