A Study of Workflow-Integrated Artificial Intelligence for RPM Enrollment

Nursing Clinical Trial

Official title:

Pragmatic Analysis of the Impact and Utilization of Workflow-Integrated Artificial Intelligence for RPM Enrollment

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT05744180
• Other study ID #: 22-008014
• Status: Enrolling by invitation
• Phase: N/A
• Start date: June 19, 2023
• Est. completion date: December 2024

Study information

• Verified date: July 2023
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 300
• Est. completion date: December 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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).

Exclusion Criteria:

• < 18 years old.

Related Conditions & MeSH terms

• Nursing

Intervention

Other:
• Interventional
The FitScore is a machine learning algorithm embedded within the electronic health record that identifies patients most likely to benefit from remote patient monitoring.

Locations

Country	Name	City	State
United States	Mayo Clinic Minnesota	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	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).	1 year
Secondary	Assessment of "fit" score overall effect on nursing efficiency and clinical workflows	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).	1 year

External Links

•   Mayo Clinic Clinical Trials