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Impact of Resident Participation in Post-ICU Follow Up Clinic

Primary Purpose

Professional Burnout

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Encounter visit with Patients
Non-encounter surveys
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Professional Burnout focused on measuring Perceptions of critical care, Professional fulfillment.

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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 Exclusion Criteria for Residents: - Provided only "cross-cover" for the patient.

Sites / Locations

  • University of MichiganRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Residents meet ICU patients during follow-up visit (encounter)

Residents in the non-encounter group

Arm Description

Residents will be paired according to the patient that were cared.

Residents will not meet with patients that were in the ICU.

Outcomes

Primary Outcome Measures

Changes in the Professional Fulfillment Scale
The 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 Scale
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.

Secondary Outcome Measures

Full Information

First Posted
January 27, 2023
Last Updated
May 17, 2023
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT05713669
Brief Title
Impact of Resident Participation in Post-ICU Follow Up Clinic
Official Title
Impact of Resident Participation in Post-ICU Follow Up Clinic
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Professional Burnout
Keywords
Perceptions of critical care, Professional fulfillment.

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Residents meet ICU patients during follow-up visit (encounter)
Arm Type
Experimental
Arm Description
Residents will be paired according to the patient that were cared.
Arm Title
Residents in the non-encounter group
Arm Type
Other
Arm Description
Residents will not meet with patients that were in the ICU.
Intervention Type
Behavioral
Intervention Name(s)
Encounter visit with Patients
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Non-encounter surveys
Intervention Description
Surveys will be completed pre and post patient follow-up.
Primary Outcome Measure Information:
Title
Changes in the Professional Fulfillment Scale
Description
The survey consists of 6 questions that are measured on a 5 point Likert scale (scored 0 to 4, with 4 representing higher fulfillment).
Time Frame
Baseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visit
Title
Changes in the Burnout Scale
Description
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.
Time Frame
Baseline (pre-post ICU follow-up visit), approximately 14 days post patient's follow-up visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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 Exclusion Criteria for Residents: - Provided only "cross-cover" for the patient.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maddie Lagina, MD
Phone
734-763-9077
Email
laginam@med.umich.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jakob McSparron, MD
Phone
734-763-9077
Email
jmcsparr@med.umich.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jakob McSparron, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maddie Lagina, MD
Phone
734-763-9077
Email
laginam@med.umich.edu
First Name & Middle Initial & Last Name & Degree
Maddie Lagina, MD
First Name & Middle Initial & Last Name & Degree
Jakob McSparron, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of Resident Participation in Post-ICU Follow Up Clinic

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