A study on the feasibility and the satisfaction of portable sleep device

A comparative study on the feasibility and the satisfaction of patients of portable sleep device according to the test location: a pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002914

Enrollment

Registered

2018-06-05

Start date

2017-07-10

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Study participants are classified into two groups of A and B. All participants who belong to these two groups underwent two sleep tests. Participants in Group A first undersent in-lab

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: male gender, no history of previous sleep testing or treatment for OSA, and high risk of moderate to severe OSA.

Exclusion criteria

Exclusion criteria: age under 20 years, heavy drinkers (more than 3 times per week), and individuals who had or were diagnosed with a skin allergy, congestive heart failure, chronic obstructive pulmonary disease, neuromuscular disease, or psychiatric disease.

Design outcomes

Primary

Measure	Time frame
feasibility and the satisfaction of patients of portable sleep device according to the test location	—

Secondary

Measure	Time frame
Agreement of sleep variables between in-hospital sleep examination and home sleep examination.	—

Countries

Korea, Republic of

Contacts

Public ContactDAE WUI YOON

Seoul National University

9286392a@hanmail.net+82-2-740-8299

Outcome results