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Impact of Resident Participation in Post-ICU Follow Up Clinic

Impact of Resident Participation in Post-ICU Follow Up Clinic

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05713669
Enrollment
30
Registered
2023-02-06
Start date
2023-03-01
Completion date
2027-04-01
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Professional Burnout

Keywords

Perceptions of critical care, Professional fulfillment.

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.

Interventions

BEHAVIORALEncounter visit with Patients

Participants in this encounter group will be asked to complete a pre and post-intervention survey, participate in a meeting with a former ICU patient at a post-ICU clinic, and undergo an in-person interview within fourteen days following the encounter.

BEHAVIORALNon-encounter surveys

Surveys will be completed pre and post patient follow-up.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

A Total of 20 residents will be recruited (10 residents in the intervention arm; 10 residents in the control arm). One resident in each pair will be randomized to participate in a follow up encounter in the post-ICU clinic with the patient that residents have cared for (intervention) and one will have no follow up encounter (control). There will be 10 patients enrolled for the study and will not be randomized into any arm. Outcomes are based on the residents only.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

for Patients: \- Must be eligible for Post ICU Longitudinal Survivor Experience (PULSE) clinic follow up and/or have received referral to clinic Inclusion criteria for Residents: * Must have completed at least one 2-week rotation in the medical ICU at the University of Michigan * Must have cared for an enrolled patient in the study

Exclusion criteria

for Patients: \- Died during ICU stay

Design outcomes

Primary

MeasureTime frameDescription
Changes in the Professional Fulfillment ScaleBaseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visitThe survey consists of 6 questions that are measured on a 5 point Likert scale (scored 0 to 4, with 4 representing higher fulfillment).
Changes in the Burnout ScaleBaseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visitThis 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.

Countries

United States

Contacts

CONTACTMaddie Lagina, MD
laginam@med.umich.edu734-763-9077
CONTACTJakob McSparron, MD
jmcsparr@med.umich.edu734-763-9077
PRINCIPAL_INVESTIGATORJakob McSparron, MD

University of Michigan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026