KCT0008472
Completed
未知
Development and Effectiveness of a Mobile app-Based Myofunctional Therapy Program for Improving Obstructive Sleep Apnea
ConditionsDiseases of the nervous system
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the nervous system
- Sponsor
- Pusan National University
- Enrollment
- 26
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Inclusion Criteria
- •Individuals who understand the purpose of this study and agree to participate.
- •Individuals diagnosed with obstructive sleep apnea by a sleep specialist based on the results of a sleep study, and who have been recommended myofunctional therapy by the sleep specialist.
- •Adults aged 18 years or older.
- •Individuals with no communication disabilities.
- •Individuals who can attach the sleep study device to at least one finger and wrist.
- •Individuals who have a mobile phone capable of running the mobile app (Android or iOS) and can use it without assistance.
Exclusion Criteria
- •Exclusion Criteria
- •Individuals with severe nasal obstruction or facial deformities confirmed by imaging studies.
- •Individuals whom the sleep specialist determines to be unable to perform myofunctional therapy due to musculoskeletal disorders.
- •Individuals with autonomic nervous system dysfunction, peripheral neuropathy, vascular disease, heart disease, or lung disease.
- •Individuals taking medications that may affect peripheral arterial tone (adrenergic blockers).
- •Types of adrenergic blockers: Tolazoline, Trazodone, Phenoxybenzamine, Phentolamine, Doxazosin, Silodosin, Alfuzosin, Tamsulosin, Terazosin, Prazosin, Mirtazapine, Atipamezole, Yohimbine, Idazoxan, Labetalol, Carvedilol.
- •(Note: Criteria 3 and 4 are exclusion criteria to prevent errors that may occur when using portable sleep study devices.)
Outcomes
Primary Outcomes
Not specified
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