OSAHS Screening in Diverse Populations
Screening for Obstructive Sleep Apnea-hypopnea Syndrome - for Community Populations, Patients With Specific Diseases and Special Populations
2 other identifiers
observational
100,000
1 country
2
Brief Summary
The goal of this prospective observational study is to learn about the current prevalence of obstructive sleep apnea-hypopnea syndrome in community population, patients with specific diseases and special population from China. The main question it aims to answer is: (1) What are the prevalence and clinical characteristics of OSA in the community population, the specific disease population and the special population respectively? (2) How about the application value of each OSA screening questionnaire for different populations?Participants will all complete a screening questionnaire, and some will be selected by random sampling to complete either a polysomnography (PSG) or a portable sleep monitor (PM).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
Typical duration for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2024
CompletedFirst Submitted
Initial submission to the registry
June 6, 2025
CompletedFirst Posted
Study publicly available on registry
July 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2027
July 30, 2026
July 1, 2026
2.9 years
June 6, 2025
July 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Apnea-Hypopnea Index (AHI)
Collected from polysomnography (PSG) or home sleep apnea testing (PM) for the diagnosis of obstructive sleep apnea (OSA). Unit of Measure: events/hour
Baseline
Lowest Oxygen Saturation (Lowest SpO₂)
Collected from PSG or PM to evaluate nocturnal hypoxemia. Unit of Measure: %
Baseline
Secondary Outcomes (3)
Diagnostic Value of the CNCQ-OSA Questionnaire
Baseline
Diagnostic Value of the STOP-Bang Questionnaire
Baseline
Diagnostic Value of the NoSAS Score
Baseline
Study Arms (3)
community population
registered community populations aged 18-80 years old.
patients with specific diseases
patients with hypertension, diabetes, cardiovascular and cerebrovascular diseases, chronic obstructive pulmonary disease, asthma and other OSA related comorbidities, aged 18-80 years old.
special population
Including college teachers and students, doctors and nurses, and company employees, aged 18-80 years old.
Interventions
In order to explore the prevalence of OSA in patients with different comorbid diseases, this study set up this observation group.
Eligibility Criteria
Target participants were recruited from multiple centers: Community population: A random number table method is used to select several communities within the designated research area. The research team then obtains a complete list of registered residents in these communities as the sampling frame. A computer-based random number generator is utilized to randomly select target residents. Patients with specific diseases: hypertension, diabetes, cardiovascular and cerebrovascular diseases, chronic obstructive pulmonary disease, asthma and other OSA related comorbidities. Special population: Including college teachers and students, doctors and nurses, and company employees.
You may qualify if:
- Sign the informed consent form before participating in the study
- Complete independent behaviour and cognitive abilities
- Ability to answer the questionnaire completely and accurately
You may not qualify if:
- Incomplete answers to the scale
- Patients with severe diseases and acute infections or those requiring long-term home oxygen therapy
- Patients with severe mental and psychological disorders
- Patients with severe organ failure
- patients with a total sleep time \<240 min by PSG or PM
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Kang Wulead
Study Sites (2)
The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, China
Anshun People's Hospital
Anshun, Guizhou, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Nuofu Zhang, professor
The First Affiliated Hospital of Guangzhou Medical University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 2 Days
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
June 6, 2025
First Posted
July 30, 2026
Study Start
September 1, 2024
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
August 1, 2027
Last Updated
July 30, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, CSR
all IPD that underlie results in a publication