Comparative Effectiveness of Readmission Reduction Interventions for Individuals with Sepsis or Pneumonia

Not Applicable

Completed

• Conditions: Lower Resp Tract Infection; Sepsis; Pneumonia; Covid19

• Registration Number: NCT04829188
• Lead Sponsor: University of Pittsburgh

Brief Summary

An adaptive platform trial to compare effectiveness of different care models to prevent readmissions for patients hospitalized with sepsis or lower respiratory tract infection. The primary outcome is number of days spent at home within 90 days after hospital discharge.

Detailed Description

This study implements an adaptive platform trial to compare effectiveness of different care models to prevent readmissions for patients hospitalized with sepsis or lower respiratory tract infection and discharged to home (with or without a short stay in a skilled nursing facility prior to going home): structured telephone support (STS); low-intensity remote patient monitoring (RPM-Low); and high-intensity remote patient monitoring (RPM-High). The remote patient monitoring models will be staffed by a physician or a nurse (Standard Team) or by a dedicated nurse-practitioner (NP)-led multidisciplinary team (Enhanced Team). Patients will be randomized to one of five arms: STS, RPM-Low + Standard Team, RPM-Low + Enhanced Team, RPM-High + Standard Team, and RPM-High + Enhanced Team. Using response adaptive randomization (RAR), interim outcome results will be used to modify the random allocation of patients to each study arm. The primary outcome is number of days spent at home within 90 days after hospital discharge. Patient-reported functional status and quality of life data will be collected in addition to electronic health record (EHR) and claims-based data to measure health care utilization. Qualitative interviews with patients and providers will provide insight into the effectiveness of the implementation process.

Study Timeline

• Study First Submitted: 2021-03-26
• Study Start: 2021-03-30
• Study First Submitted QC: 2021-04-01
• Study First Posted: 2021-04-02
• Primary Completion: 2024-12-15
• Study Completion: 2024-12-15
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-14
• Last Update Posted: 2025-01-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1288

Inclusion Criteria

• UPMC Health Plan members
• Medicare Fee-for-Service enrollees
• Age 21+ -Hospitalized with a primary diagnosis of sepsis or lower respiratory tract infection, --
• Discharged to home, independent living facility, or skilled nursing facility
• Readmission risk is moderate or high

Exclusion Criteria

• Admitted from hospice;
• Discharged to hospice, inpatient rehabilitation, or a long term acute care facility;
• Known to be pregnant;
• Current enrollment in another remote patient monitoring program;
• Failure of the Callahan 6 item cognitive screen and do not have a proxy to consent;
• No access to a technological device required to participate in remote patient monitoring program;
• Current enrollment in UPMC Advanced Illness Care program;
• Severe, persistent cognitive impairment;
• No documented PCP;
• PCP disapproves of the patient being enrolled in remote patient monitoring;
• Discharged from hospital to skilled nursing facility and stay at the skilled nursing facility for greater than 28 days

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Post-discharge home days	90 days after discharge to home	days alive and at home

Secondary Outcome Measures

Name	Time	Method
Mortality	measured at 90 days	Mortality will be assessed via claims data to see if and when the member/participant passes away.
Functional Status (measured by PROMIS Physical Function-for Mobility Aid Users-SF)	baseline, 90 days	Functional Status will be measured using the Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function - for Mobility Aid Users-SF. This measures one's ability to stand, walk, and perform activities of daily living if some participants utilize mobility aids such as wheelchairs. The minimum score for patients who can walk 25 feet is 11 and the maximum 55. The minimum score for patients who cannot walk 25 feet is 8 and the maximum score is 40. Higher scores indicate better function status for both groups.
Transition to Hospice	measured at 90 days after discharge to home	Transition to Hospice will be assessed via health insurance claims.
Health-related Quality of Life (measured by Quality of Life Enjoyment and Satisfaction Questionnaire-SF)	baseline, 90 days	Health-related Quality of Life will be measured using the Quality of Life Enjoyment and Satisfaction Questionnaire-SF. The Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) is a self-report measure designed to enable investigators to easily obtain sensitive measures of the degree of enjoyment and satisfaction experienced by subjects in various areas of daily functioning. The Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (Q-LES-Q-SF) is a 16 item self-administered questionnaire that captures life satisfaction over the past week. Each question is rated on a 5 point scale from 1 (Very Poor) to 5 (Very Good). A total score is derived from 14 items with a maximum score of 70 and with higher scores indicating greater life satisfaction and enjoyment.
Emergent outpatient utilization	measured at 90 days after discharge to home	Emergent outpatient utilization includes emergency department visits and urgent care visits. It will be assessed via claims data at 90 days for study participants.
Hospital readmissions	measured at 90 days	Readmissions will be assessed via health insurance claims for any inpatient admissions after index admission.

Trial Locations

Locations (1)

UPMC Presbyterian; 🇺🇸 Pittsburgh, Pennsylvania, United States