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Clinical Trials/NCT02136186
NCT02136186
Completed
Not Applicable

Home Telemonitoring in Patients at High Risk for Readmission

Mayo Clinic1 site in 1 country1,380 target enrollmentOctober 2014
ConditionsInpatients

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Inpatients
Sponsor
Mayo Clinic
Enrollment
1380
Locations
1
Primary Endpoint
Changes in Readmissions into Hospital
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study will evaluate the efficacy of home telemonitoring as an intervention to decrease hospital readmissions in patients at high risk for readmission. The overall readmission rate for high-risk MCF hospital patients is approximately 20%. Currently a system is in place to identify and score all MCF patients for their risk of readmission. This score is based on multiple variables including but not limited to: co-morbid conditions, patient's health literacy, whether they are a Medicare/Medicaid patient, their in-home social support, and whether they have had prior hospital admissions within the previous year. The literature shows that home telemonitoring of patients has had mixed results for effectiveness at preventing hospitalizations and emergency department visits. Many of these reports have restricted studies to patients with specific diseases or general characteristics; some have shown improved results while others have not. No study has examined patients who are high risk for readmission to determine if home telemonitoring for 30 days post-discharge reduces the risk for 30-day readmission.

Detailed Description

We hope to enroll a total of 1900 participants, 950 in each arm, over the next 2 years. One arm will be the telemonitoring group and one arm will be the standard of care group. Participants will be in the study for 30 days. Participants in the telemonitoring group will receive a Telestation, blood pressure monitor, and pulse oximeter. If the participant also has congestive heart failure, they will receive a scale. All of these vital measurements are to be taken on a daily basis along with survey questions on how the patient feels. If set parameters are out of the normal range, a flag will trigger that requires follow up/intervention from a nurse by telephone. In some cases, the participant might need to come back in to see a physician through the outpatient clinic. The participant in the standard of care group will be contacted via phone 30 days after discharge to learn if they were readmitted to any hospitals or had any emergency room visits during the past 30 days. This data will be collected via Philips software and also entered into the RedCap database here at Mayo Clinic.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
July 31, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nancy L. Dawson, M.D.

PI

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • readmission risk score of 11 or higher 2) may be from any service in the hospital 3) patient discharged home or 4) patient discharged to skilled nursing/rehabilitation

Exclusion Criteria

  • international
  • under age 18
  • discharged to hospice
  • discharged to a sub-acute care hospital
  • transferred to an acute care hospital or
  • if the patient has a planned readmission within the next 30 days

Outcomes

Primary Outcomes

Changes in Readmissions into Hospital

Time Frame: 30 days

Compare 30-day readmission rates between high-risk patients who are home monitored using technology and high-risk patients who receive the current standard care.

Secondary Outcomes

  • Changes in Readmissions in the Emergency Room(30 days)

Study Sites (1)

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