Digital-supported Orofacial Myofunctional Therapy in OSA
Recruiting
N/A
Interventional Study
Obstructive Sleep Apnea (OSA)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 60 (estimated)
- Sponsor
- Hong Kong Metropolitan University · Other
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About This Trial
This pilot study explores the feasibility, acceptability, and preliminary effectiveness of Digital-supported Orofacial Myofunctional Therapy (d-MFT), an innovative program combining facial recognition technology with evidence-based orofacial exercises for individuals with mild to moderate obstructive sleep apnoea (OSA). The d-MFT program aims to strengthen oropharyngeal muscles, improve airway fun…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adults aged 18 years and above
* Diagnosed with mild to moderate Obstructive Sleep Apnoea, defined as: Apnoea-Hypopnea Index of 5-30 events per hour
* Indications for Continuous Positive Airway Pressure or oral appliance treatment, but unable to tolerate or decline these treat…
Contacts