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Clinical Trials/KCT0008472
KCT0008472
Completed
未知

Development and Effectiveness of a Mobile app-Based Myofunctional Therapy Program for Improving Obstructive Sleep Apnea

Pusan National University0 sites26 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
May 8, 2024
Last Updated
last year
Study Type
Interventional Study
Sex
All

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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