A Study of Workflow-Integrated Artificial Intelligence for RPM Enrollment

Not Applicable

Completed

• Conditions: Nursing
• Interventions: Other: Interventional

• Registration Number: NCT05744180
• Lead Sponsor: Mayo Clinic

Brief Summary

The objective of this study is to evaluate effectiveness, usability and clinical utility of the remote patient monitoring (RPM) "fit" score when choosing patients to enter the RPM Program.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2023-02-02
• Study First Submitted QC: 2023-02-15
• Study First Posted: 2023-02-24
• Study Start: 2023-06-19
• Primary Completion: 2024-01-16
• Study Completion: 2024-01-16
• Status Verified: 2024-10
• Last Update Submitted: 2024-10-07
• Last Update Posted: 2024-10-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• The study participants will be nurses who are part of the RPM care team that cares for adult patients ≥18 years.
• A patient's data will be included in the analysis if the patient is ≥18 years old and receives care from a participating nurse.
• Patient data will only be collected if permitted (based on the use of the Minnesota Research Authorization Retrieval Tool).
• Patients who will be considered for this study will be assessed based on standard RPM program inclusion and exclusion criteria for the any of the chronic disease RPM programs (congestive heart failure, coronary artery disease, hypertension, type 2 diabetes, COPD, and general complex care).

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Exclusion Criteria

• < 18 years old.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Arm Not Applicable	Interventional	-

Primary Outcome Measures

Name	Time	Method
Evaluation of the effectiveness, usability, and clinical utility of the RPM "fit" score as displayed in the Acute Multipatient Viewer (AMP) and underlying AI models in the real-world setting	1 year	FitScore effectiveness will determined by the patient care utilization outcomes of those who did or did not participate in RPM (for those enrolled with or without the FitScore). Usability and clinical utility will be self-reported by nursing staff collected through surveys or as directly observed by study staff (as to experience with or without the FitScore).

Secondary Outcome Measures

Name	Time	Method
Assessment of "fit" score overall effect on nursing efficiency and clinical workflows	1 year	Efficiency will be measured by timing studies of nurse patient screening for RPM eligibility as directly observed by study staff. The effect on clinical workflows will be self-reported by nursing staff collected through surveys (as to experience with or without the FitScore).

Trial Locations

Locations (1)

Mayo Clinic Minnesota; 🇺🇸 Rochester, Minnesota, United States