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Clinical Outcomes of Continuous Positive Airway Pressure for Obstructive Sleep Apnoea

Clinical Outcomes of Continuous Positive Airway Pressure for Obstructive Sleep Apnoea in Chinese Adults

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001111460
Enrollment
40
Registered
2025-10-13
Start date
2025-10-27
Completion date
2026-07-27
Last updated
2025-10-27

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

Conditions

None listed

Brief summary

This project will investigate the sleep and cardiovascular effects of obstructive sleep apnoea treatment (OSA) treatment in Chinese adults, and whether these outcomes differ in those observed in a similar group of Caucasian adults. All participants will receive continuous positive airway pressure (CPAP) treatment for the 12-week duration of the study. Sleep, cardiovascular, and metabolic health outcomes will be assessed before and after CPAP treatment. the aim of this study is to assess whether treatment of OSA in Chinese patients improves clinical outcomes, and whether these effects differ from those reported in a Caucasian population.

Interventions

This project will investigate the sleep and cardiovascular effects of obstructive sleep apnoea treatment (OSA) treatment in Chinese adults, and whether these outcomes differ in those observed in a similar group of Caucasian adults. Adults of Chinese descent (intervention) and Caucasian descent (comparator) with newly diagnosed moderate to severe OSA (apnoea-hypopnoea index (AHI) >15 events/hour) and prescribed CPAP will be recruited. All participants will receive continuous positive airway press

This project will investigate the sleep and cardiovascular effects of obstructive sleep apnoea treatment (OSA) treatment in Chinese adults, and whether these outcomes differ in those observed in a similar group of Caucasian adults. Adults of Chinese descent (intervention) and Caucasian descent (comparator) with newly diagnosed moderate to severe OSA (apnoea-hypopnoea index (AHI) >15 events/hour) and prescribed CPAP will be recruited. All participants will receive continuous positive airway pressure (CPAP) treatment for the 12-week duration of the study. CPAP involves using a machine to deliver a continuous flow of pressurized air through a mask to keep the airway open during sleep, used to treat obstructive sleep apnea (OSA). The pressurized air prevents the airway from collapsing, allowing for uninterrupted breathing. CPAP will be used for all periods of sleep including naps over the 12-week study period. The CPAP machine setup and mask fitting will be performed by a CPAP therapist (sleep scientist) for each participant at the start of the 12-week trial. Sleep, cardiovascular, and metabolic health outcomes will be assessed pre and post CPAP treatment. The primary outcome of this study is change in blood pressure following CPAP treatment, with secondary outcomes including anthropometry, cardiovascular biomarkers, and sleep quality. CPAP adherence is monitored through data download from the CPAP machine itself, which tracks usage hours, mask leaks, and the pressure setting.

Sponsors

A/Professor Denise O'Driscoll - Eastern Health
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Newly diagnosed with moderate to severe Obstructive Sleep Apnoea (AHI>15events/h) and prescribed CPAP.

Exclusion criteria

- Pregnancy / breastfeeding - Had previous weight loss surgery - history of eating disorders - using anti-obesity medications - diagnosis of T1D and insulin-dependent T2D, or any medication that could interfere with weight loss (on acase by case basis), - renal failure, heart failure, recent MI/stroke (within previous 6months), - routine shiftwork, - active psychiatric condition or intellectual disability that would prevent them from following the study protocol. - Unwilling or unable to provide informed consent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026