Skip to content

Effective Conversion of Individuals at Risk

Effective Conversion of Individuals at Risk

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05112757
Enrollment
77
Registered
2021-11-09
Start date
2022-02-24
Completion date
2022-12-08
Last updated
2022-12-12

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

Conditions

Atrial Fibrillation, Obstructive Sleep Apnea

Keywords

OSA, AFib

Brief summary

This study aims to guide participants in recognizing their OSA (obstructive sleep apnea) and AFib (atrial fibrillation) symptoms, realizing what medical conditions can cause these symptoms (if any) and inform the participants on their possible diagnosis

Detailed description

The primary objective is to analyze how many patients at risk of medical conditions will be converted to a health care professional by a smartphone application. Historical data (number of patients at risk of OSA and/or AFib that seeked help for their condition in the past year) from institute will be used as a reference. We will refer to this as the 'baseline conversion rate', reflecting the natural transition of patients in the general healthcare system.

Interventions

OTHERSmartphone application use

Use of a smartphone application

Sponsors

Sanford Health
CollaboratorOTHER
Philips Electronics Nederland B.V. acting through Philips CTO organization
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* High risk of OSA and/or AFib, as defined by the risk algorithm developed by Sanford health * 18 years or older, with sufficient English language skills * Owning a smartphone with a relatively new operating system (iOS v. 14 (Iphone 6S or higher) or an Android device v.11\<) * Able to download and handle an app on a smartphone * Willing and able to give informed consent

Exclusion criteria

* Diagnosed with OSA and/or AFib * Diagnosed health issues that are potentially life threatening or causing mental issues (stroke, Alzheimer's Disease, depression, etc.) * Pregnancy/breast feeding

Design outcomes

Primary

MeasureTime frameDescription
Effective conversion6 months after consentNumber of patients that visited the Primary Care Physician

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026