Mouth exercises vs. CPAP: new study aims to ease sleep apnea without machines
NCT ID NCT07539870
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether orofacial myofunctional therapy (OMT) – exercises for the mouth and tongue – can improve sleep apnea symptoms in adults with mild-to-moderate cases. It will compare OMT alone, CPAP alone, both together, and standard care in 168 participants over 12 weeks. The goal is to see if these treatments reduce breathing pauses during sleep and improve jaw movement.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 168 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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May 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older. * Mild-to-moderate OSA (AHI 5.0-29.9 events/hour) confirmed by Type I polysomnography. * Protrusive excursion of at least 5 mm measured with the George Gauge. * No previous treatment with CPAP or OMT. * Ability to perform oropharyngeal exercises. * Written informed consent. Exclusion Criteria: * Severe obstructive sleep apnea (AHI 30 events/hour or higher) or urgent need for CPAP * Suspected or confirmed obesity hypoventilation syndrome, chronic ventilatory failure, or severe obesity associated with daytime hypercapnia or hypoxemia * Clinically significant insomnia, defined as an Insomnia Severity Index (ISI) score \> 14 at screening. * Uncontrolled psychiatric or neurological conditions likely to substantially affect sleep quality or daytime symptoms independently of OSA (e.g., major depressive episode, severe anxiety disorder, chronic disabling migraine)., as judged by the investigator. * Current use of medications likely to affect sleep architecture, respiratory drive, or PAP tolerance, including chronic opioid therapy and other sedative medications judged incompatible with study participation. * Unstable or severe cardiovascular disease requiring priority standard management, including poorly controlled arrhythmia, nocturnal angina, decompensated heart failure, treatment-resistant hypertension, or recent acute coronary syndrome * Uncontrolled diabetes mellitus requiring treatment intensification, for example - HbA1c greater than 10% and/or symptomatic hyperglycemia * Neurological or ear-nose-throat disease affecting the upper airway * Craniofacial abnormalities * Maxillofacial surgery within the previous 6 months * Temporomandibular pain preventing completion of exercises * Active periodontitis * Pregnancy * Foreseeable non-adherence to the intervention * Inability to use CPAP despite standard fitting and troubleshooting, or any contraindication to CPAP treatment. * Ongoing CPAP or OMT at inclusion
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
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The official record
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