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A Study of Workflow-Integrated Artificial Intelligence for RPM Enrollment

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Mayo Clinic

Status

Completed

Conditions

Nursing

Treatments

Other: Interventional

Study type

Interventional

Funder types

Other

Identifiers

NCT05744180
22-008014

Details and patient eligibility

About

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.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Arm Not Applicable
Other group
Treatment:
Other: Interventional

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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