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Effect of Smart Watch and App on PAP Adherence in OSA (Watch-OSA)

Seoul National University logo

Seoul National University

Status

Enrolling

Conditions

Obstructive Sleep Apnea of Adult
Adherence, Treatment
Smart Watch
Positive Airway Pressure

Treatments

Device: the smart watch and Samsung Health app

Study type

Interventional

Funder types

Other

Identifiers

NCT05530265
22070571340

Details and patient eligibility

About

Continuous positive airway pressure (CPAP) is highly effective in treating obstructive sleep apnea (OSA). However, this treatment modality relies heavily on patient adherence, and poor adherence to the treatment limits its effectiveness in treating OSA. Strategies to augment adherence are needed in the management of OSA.

The smart watch and linked app provide various health information, including sleep, snoring or oxygen saturation during sleep, exercise, blood pressure, and electrocardiogram. The smart watch and linked app could potentially improve adherence to positive airway pressure (PAP) treatment.

This randomized controlled trial (RCT) aimed to examine whether the use of smart watch and app can increase PAP adherence in patients with OSA.

Enrollment

92 estimated patients

Sex

All

Ages

22 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosed with OSA (apnea-hyponea index [AHI])≥ 5 /h) by type 1 polysomnography
  • no prior use of PAP (CPAP or auto-adjusting PAP [APAP]), or no prior use of PAP within the previous 90 days in patients who had received PAP therapy, or current PAP users with average daily usage (all days) < 4 hours within the previous 90 days

Exclusion criteria

  • patients who refuse PAP therapy
  • patients who have used a smart watch (e.g., Galaxy Watch, Apple Watch, etc.) within the previous 90 days
  • patients with central sleep apnea or neuromuscular disease
  • patients receiving supplemental oxygen therapy due to underlying diseases including heart failure, stroke, chronic obstructive pulmonary disease, interstitial pulmonary disease, hypoventilation syndrome, or whose baseline oxygen saturation is less than 90%
  • patients with implanted cardiac pacemakers, defibrillators, or other electronic devices
  • patients who are inexperienced in using smartphones, apps, or smart watches
  • patients with an inability or unwillingness to provide informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

92 participants in 2 patient groups

Smart watch group
Experimental group
Description:
The user of the smart watch and Samsung Health app
Treatment:
Device: the smart watch and Samsung Health app
Usual care
No Intervention group
Description:
No use of both the smart watch and Samsung Health app

Trial contacts and locations

1

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Central trial contact

Jaeyoung Cho, M.D., Ph.D.

Data sourced from clinicaltrials.gov

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