Effective Conversion of Individuals at Risk

Not Applicable

Terminated

• Conditions: Atrial Fibrillation; Obstructive Sleep Apnea
• Interventions: Other: Smartphone application use

• Registration Number: NCT05112757
• Lead Sponsor: Philips Electronics Nederland B.V. acting through Philips CTO organization

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.

Study Timeline

• Study First Submitted: 2021-10-19
• Study First Submitted QC: 2021-11-04
• Study First Posted: 2021-11-09
• Study Start: 2022-02-24
• Status Verified: 2022-12
• Primary Completion: 2022-12-08
• Study Completion: 2022-12-08
• Last Update Submitted: 2022-12-08
• Last Update Posted: 2022-12-12

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 77

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

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Intervention	Smartphone application use	Smartphone app use

Primary Outcome Measures

Name	Time	Method
Effective conversion	6 months after consent	Number of patients that visited the Primary Care Physician

Trial Locations

Locations (1)

Sandford Health; 🇺🇸 Sioux Falls, South Dakota, United States