Cost-effectiveness Analysis of Home Polysomnography Made by Primary Care - (SONOPC Study)
Starting soon · Not applicable
Conditions studied: Obstructive Sleep Apnea (OSA)
In brief
The goal of this randomized clinical trial is to assess the cost-effectiveness of a home polyssomnography made by primary care compared to standard protocol for diagnosing obstructive sleep apnea in both genders. Researchers will compare if a polyssomnography made by primary care is more cost-effective than standard protocol to see if this strategy decrease the wait time to get this exam in public health system in Brazil . Participants will undergo diagnostic screening using the STOP-BANG and Epworth questionnaires; following the identification of apnea risk, they will be randomized into two groups: one group will undergo the examination via the health department's scheduling system, while the other will do so through primary health care services at the unit closest to their residence.
Key facts
- Study ID
- NCT07744880
- Run by
- Escola Superior de Ciencias da Saude
- People needed
- 60
- Starts
- 2026-09-01
- Expected to finish
- 2027-09-30
- Last updated by the study team
- 2026-08-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- aged 18 years or older;
- present clinical suspicion of OSA, confirmed by screening using the STOP-BANG and Epworth Sleepiness Scale questionnaires;
- be receiving care at Basic Health Units (UBS), or be registered on the Central Regulation waiting list system for polysomnography (PSG);
You may not qualify if…
- use of home oxygen therapy;
- use of invasive or non-invasive mechanical ventilation;
- use of a tracheostomy;
- change of residence during the data collection period;
- known allergy to materials used in sleep monitoring equipment.
Full record on ClinicalTrials.gov
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