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Application of the Patient-reported Longitudinal Assessment Tool for OSA (PLATO) Questionnaire in Oral Appliance Therapy for Obstructive Sleep Apnea
Application of the PLATO Questionnaire in Oral Appliance Therapy for Obstructive Sleep Apnea
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: Inclusion Criteria * All ethnicities and genders * 18 years of age * AHI ≥5 ≤ 30 * Dentally suitable for OAT * AHI \> 30 if refusal or intolerance for CPAP therapy * Smartphone ( for home sleep test) * Only using oral appliance therapy (i.e., no combination therapy) Exclusion Criteria: * Pregnancy * Use of home oxygen * Serious/uncontrolled illness (such as angina/myocardial infarction, cancer, stroke, dementia, congestive heart failure, chronic respiratory illness), significant sleep-related disorder) * The investigator feels, for any reason, that the patient's participation may not be in their best interests * Any condition or circumstance that, in the opinion of the investigator, is likely to preclude study completion, prevent accurate data collection, or bias the results
About the study
Prospective, real-world observational study in a dental sleep practice to assess the feasibility of incorporating the PLATO into a dental sleep practice and applicability for patients who are undergoing oral appliance therapy for the treatment of obstructive sleep apnea(OSA).
The PLATO questionnaire was recently developed by the American Academy of Sleep Medicine specifically for use in patients with obstructive sleep apnea.
What is being tested
- The study will assess the feasibility of incorporating the PLATO questionnaire into a dental sleep practice. The PLATO questionnaire was developed as a patient reported outcome measure (other)
Sponsor: Nevada Dental Sleep · Participants: 20 · Started: Oct 1, 2026
Contact the study team
Official record on ClinicalTrials.gov — NCT07789834
Locations in the U.S.
| Nevada | Nevada Dental Sleep, Henderson |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.