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Effect of Positive Attitudes on Behavior and Wellness (TEAM-ICU)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04441632
Recruitment Status : Completed
First Posted : June 22, 2020
Last Update Posted : August 12, 2020
Sponsor:
Information provided by (Responsible Party):
Jack Green, Cedars-Sinai Medical Center

Brief Summary:
The COVID-19 pandemic has undoubtedly elevated levels of stress to people all over the globe, but none more than to the providers on the front-line. The purpose of the study is to first, assess the effects of the pandemic on burnout, team cohesion, and resiliency among healthcare providers battling COVID-19 together in a medical ICU (MICU). Secondly, the investigators hope to then assess the effects of simple positive feedback on transforming culture and attitudes during times of major stress.

Condition or disease Intervention/treatment Phase
Burnout Stress, Emotional Behavioral: Positive feedback Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 24 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: The Impact of Positive Reinforcement on Teamwork Climate, Resiliency, and Burnout During the COVID-19 Pandemic: the TEAM-ICU Study (Transforming Employee Attitudes Via Messaging Strengthens Interconnection, Communication, and Unity)
Actual Study Start Date : June 15, 2020
Actual Primary Completion Date : July 26, 2020
Actual Study Completion Date : July 30, 2020

Arm Intervention/treatment
Positive feedback
Participants in the study will provide consistent positive feedback to the colleagues they work with in the medical ICU (MICU) over a 4 week duration.
Behavioral: Positive feedback
Participants will submit positive feedback comments to their colleagues (anonymously or signed, participant-dependent) through an anonymous survey link, a minimum of twice weekly to 6 uniquely different individuals over a 4 week period (total minimum 24 unique individuals over the study period).




Primary Outcome Measures :
  1. Teamwork climate, as measured by selected items from the validated Safety Attitude Questionnaire (SAQ) [ Time Frame: 4 weeks ]
    The SAQ measures teamwork climate, safety climate, job satisfaction, stress recognition, perceptions of management, and working conditions. The six items assessing teamwork climate will be used. 5 point likert scale is used. Mean of the items - 1 * 25 will convert each participant's results to a 100 point scale (0, 25, 50, 75, 100 points).

  2. Resiliency, as measured by the validated Brief Resilience Scale (BRS) [ Time Frame: 4 weeks ]
    The BRS is comprised of 6 items on a likert scale. Responses varying from 1-5 for all six items give a total range of 6-30. This sum will be divided by the total number of questions for a final score.

  3. Burnout, as validated by the single-item burnout scale inventory [ Time Frame: 4 weeks ]
    This single item inventory provides 5 definitions of burnout that the participant will choose that most closely fits their personal level of burnout at the moment



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Front-line healthcare providers in the Medical Intensive Care Unit (MICU): nurses, respiratory therapists, resident physicians, fellow physicians, and attending physicians

Exclusion Criteria:

  • Healthcare providers providing only consultatory care in the MICU
  • Front-line healthcare providers not working in the MICU during the study period

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04441632


Locations
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United States, California
Cedars-Sinai Medical Center
Los Angeles, California, United States, 90048
Sponsors and Collaborators
Cedars-Sinai Medical Center
Investigators
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Principal Investigator: Jack Green, MD Cedars-Sinai Medical Center
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Responsible Party: Jack Green, Assistant Professor of Pediatrics, Cedars-Sinai Medical Center
ClinicalTrials.gov Identifier: NCT04441632    
Other Study ID Numbers: STUDY00000786
First Posted: June 22, 2020    Key Record Dates
Last Update Posted: August 12, 2020
Last Verified: August 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Jack Green, Cedars-Sinai Medical Center:
wellness
healthcare
burnout
COVID
Additional relevant MeSH terms:
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Burnout, Psychological
Stress, Psychological
Behavioral Symptoms