Impact of Resident Participation in Post-ICU Follow Up Clinic
- Conditions
- Professional Burnout
- Interventions
- Behavioral: Non-encounter surveysBehavioral: Encounter visit with Patients
- Registration Number
- NCT05713669
- Lead Sponsor
- University of Michigan
- Brief Summary
This study is being conducted to describe the impact of a meeting between patients that were admitted to the intensive care unit (ICU) and a provider that cared for the patients during the period of critical illness. The study team is aiming to describe the effect this meeting has on the physician that previously cared for the patient.
The study team hypothesizes that facilitating involvement in post-ICU clinic and creating longitudinal relationships between providers of critical care and survivors of critical illness will have positive effects on trainees, both in professional fulfillment and burnout scores and in perceptions of critical care.
- Detailed Description
Physicians and patients that had been cared for in the ICU will be enrolled in this project. Residents that are recruited will be randomized to the encounter group or the control group.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 30
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Residents in the non-encounter group Non-encounter surveys Residents will not meet with patients that were in the ICU. Residents meet ICU patients during follow-up visit (encounter) Encounter visit with Patients Residents will be paired according to the patient that were cared.
- Primary Outcome Measures
Name Time Method Changes in the Burnout Scale Baseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visit This scale has 4 questions that will indicate the level of burnout with scores from not at all =0 - extremely =4. A higher score indicates a higher sense of burnout.
Changes in the Professional Fulfillment Scale Baseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visit The survey consists of 6 questions that are measured on a 5 point Likert scale (scored 0 to 4, with 4 representing higher fulfillment).
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Michigan
🇺🇸Ann Arbor, Michigan, United States