Post-ICU Clinic Follow-Up for Reducing Doctor Burnout
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores how meetings between ICU patients and their doctors after discharge might reduce doctor burnout. It focuses on fostering ongoing relationships between doctors who provided critical care and patients who survived serious illnesses. The trial examines whether these "encounter visits with patients" improve doctors' job satisfaction and reduce stress levels. Patients referred to a special follow-up clinic after their ICU stay might be suitable candidates. As an unphased trial, this study offers patients a unique opportunity to contribute to enhancing healthcare provider well-being.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What prior data suggests that this protocol is safe for reducing doctor burnout?
Research has shown that meeting with patients after intensive care is safe and helpful. Studies on clinics that see patients post-ICU suggest these visits improve follow-up care without major safety issues. For instance, research on these clinics found that follow-ups are well-organized and effective across various healthcare systems worldwide. This indicates that having medical residents meet with former ICU patients is generally safe and does not cause harm.
While these meetings mainly benefit doctors and medical trainees, there have been no significant reports of problems during these visits. This suggests the process is safe for both healthcare providers and patients.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores a novel approach to reducing doctor burnout by focusing on post-ICU care. Traditionally, treatments for doctor burnout might include stress management workshops or wellness programs, but this trial is unique because it involves residents meeting with ICU patients during follow-up visits. This face-to-face interaction could provide valuable closure and emotional connection, potentially decreasing stress and burnout. By examining how direct patient encounters after ICU care affect residents, researchers hope to uncover a simple yet effective method to improve doctors' well-being and job satisfaction.
What evidence suggests that this trial's treatments could be effective in reducing doctor burnout?
Research has shown that clinics for patients after ICU care can help reduce burnout in healthcare workers. In this trial, some residents will meet ICU patients during follow-up visits. Studies suggest that these interactions can lower stress and improve mental health for ICU teams. One study indicated that meeting with patients after their ICU stay can increase healthcare workers' satisfaction and reduce burnout. These meetings help build strong relationships, potentially enhancing how they feel about their work in critical care. Overall, evidence supports the idea that follow-up visits positively affect healthcare providers. Meanwhile, other residents in this trial will not meet with patients, allowing for a comparison of outcomes between the two groups.12367
Who Is on the Research Team?
Jakob McSparron, MD
Principal Investigator
University of Michigan
Are You a Good Fit for This Trial?
This trial is for healthcare providers who have completed at least one 2-week rotation in the medical ICU at the University of Michigan and cared for a patient enrolled in this study. It's focused on those eligible or referred to Post ICU Longitudinal Survivor Experience (PULSE) clinic follow-up.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Follow-up Visit
Residents meet ICU patients during a follow-up visit to assess the impact on professional fulfillment and burnout
Post-Visit Assessment
Assessment of changes in Professional Fulfillment and Burnout Scales approximately 14 days after the follow-up visit
What Are the Treatments Tested in This Trial?
Interventions
- Encounter visit with Patients
- Non-encounter surveys
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Michigan
Lead Sponsor