NCT07736872

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100,000

participants targeted

Target at P75+ for all trials

Timeline
12mo left

Started Sep 2024

Typical duration for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

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 Progress66%
Sep 2024Aug 2027

Study Start

First participant enrolled

September 1, 2024

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

June 6, 2025

Completed
1.1 years until next milestone

First Posted

Study publicly available on registry

July 30, 2026

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2027

Last Updated

July 30, 2026

Status Verified

July 1, 2026

Enrollment Period

2.9 years

First QC Date

June 6, 2025

Last Update Submit

July 26, 2026

Conditions

Keywords

osbtructive sleep apneasnoringprevalencescreening questionnairesCNCQ-OSASTOP-BangNoSAS

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.

Other: patients with 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, 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.

patients with specific diseases

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Study Sites (2)

The First Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, China

RECRUITING

Anshun People's Hospital

Anshun, Guizhou, China

NOT YET RECRUITING

MeSH Terms

Conditions

Sleep Apnea, ObstructiveSnoring

Interventions

Blood Circulation

Condition Hierarchy (Ancestors)

Sleep Apnea SyndromesApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesRespiratory SoundsSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Cardiovascular Physiological PhenomenaCirculatory and Respiratory Physiological Phenomena

Study Officials

  • Nuofu Zhang, professor

    The First Affiliated Hospital of Guangzhou Medical University

    STUDY DIRECTOR

Central Study Contacts

Donghao Wang, Phd

CONTACT

Dongxing Zhao, professor

CONTACT

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

all IPD that underlie results in a publication

Shared Documents
STUDY PROTOCOL, CSR

Locations