Readmission Reduction Interventions for Sepsis or Pneumonia
(ACCOMPLISH Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests various methods to prevent hospital readmissions after treatment for sepsis or pneumonia. It compares different support systems, such as high or low-intensity remote check-ins (High-intensity Remote Patient Monitoring and Low-intensity Remote Patient Monitoring) and phone support (Structured Telephone Support), to determine which keeps patients healthier at home. Ideal participants are those hospitalized for sepsis or a lung infection and are at moderate or high risk of readmission. As an unphased trial, this study allows participants to contribute to innovative care strategies that could enhance recovery and reduce hospital readmissions.
Do I have to stop taking my current medications for this trial?
The trial protocol does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that remote patient monitoring (RPM) is generally safe and can enhance patient well-being and recovery. Studies have found that RPM helps patients adhere to their treatment plans and maintain safety. Patients using RPM often experience improved well-being and increased mobility, regardless of the monitoring frequency.
Structured Telephone Support (STS) involves regular phone calls to ensure patients adhere to their care plans after hospital discharge. This method is well established and generally safe, focusing on early detection of any issues.
Overall, these methods are well-tolerated and have been successfully implemented in healthcare. They aim to ensure patient safety and reduce the likelihood of hospital readmission after discharge.12345Why are researchers excited about this trial?
Researchers are excited about these interventions for reducing readmissions in sepsis or pneumonia patients because they offer more personalized and continuous care after hospital discharge. Unlike standard practices that may involve only periodic check-ins, these interventions use high-intensity remote patient monitoring (RPM) to frequently assess a patient's health status and proactively address issues like infection or heart and lung conditions. The Enhanced Response Team adds a new layer of care by involving a multidisciplinary team led by a certified registered nurse practitioner, who can modify care plans and provide palliative care, ensuring a comprehensive approach to managing post-discharge health. This proactive method could significantly reduce hospital readmissions by catching and addressing potential complications early.
What evidence suggests that this trial's treatments could be effective for reducing readmissions in patients with sepsis or pneumonia?
Research has shown that remote patient monitoring (RPM) can help reduce hospital readmissions. In this trial, participants may receive either high-intensity or low-intensity RPM, which involves monitoring patients' health at home, potentially reducing hospital stays and emergency visits. High-intensity RPM includes more frequent check-ins, allowing early detection of health issues. The trial also studies Structured Telephone Support (STS), which involves follow-up calls and education after hospital discharge. While RPM often has a greater impact, STS provides essential follow-up care and support, also reducing readmissions. Overall, these approaches aim to keep patients healthier at home after hospital discharge.678910
Who Is on the Research Team?
Kalpana Char, MD
Principal Investigator
UPMC Health Plan
Sachin Yende, MD
Principal Investigator
University of Pittsburgh
Are You a Good Fit for This Trial?
This trial is for adults over 21 who were hospitalized with sepsis or a lower respiratory infection, have a moderate to high risk of readmission, and are going home or to certain facilities. They must be Medicare enrollees or UPMC Health Plan members. Excluded are those with no PCP approval for RPM, pregnant women, long-term skilled nursing facility residents, lacking technology for RPM participation, severe cognitive issues without a proxy, hospice patients, and current participants in similar programs.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive structured telephone support or remote patient monitoring for up to 90 days post-discharge
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Enhanced Response Team
- High-intensity Remote Patient Monitoring (RPM-High)
- Low-intensity Remote Patient Monitoring (RPM-Low)
- Standard Response Team
- Structured Telephone Support (STS)
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Pittsburgh
Lead Sponsor
Patient-Centered Outcomes Research Institute
Collaborator