COPING With COVID-19( CWC-19)
Primary Purpose
COVID-19
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Crisis management coaching
Sponsored by
About this trial
This is an interventional other trial for COVID-19
Eligibility Criteria
Inclusion Criteria:
- Any faculty, staff, or trainee from Duke pulmonary and critical care that consents to being in the study
Exclusion Criteria:
-
Sites / Locations
- Duke University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Health Care Workers
Arm Description
Faculty, staff, and trainees dealing with COVID-19 pandemic
Outcomes
Primary Outcome Measures
Change in stress level as measured by survey
Secondary Outcome Measures
Change wellness as measured by survey
Survey is 14-items asking about wellness on a scale from "Strongly Agree" to "Not at all"
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04343690
Brief Title
COPING With COVID-19( CWC-19)
Official Title
Effectiveness of Crisis Management Coaching on Faculty and Trainee Wellness During COVID-19 Crisis
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Withdrawn
Why Stopped
Study Ended May 1, 2020 with no enrollment
Study Start Date
March 27, 2020 (Actual)
Primary Completion Date
May 1, 2020 (Actual)
Study Completion Date
May 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is 1) to understand effects of COVID-19 crisis on wellness of pulmonary and critical care faculty and trainees who are at frontline fighting this pandemic 2) Assess the effectiveness of series of weekly web based crisis management coaching from world renowned experts in coaching and 3) identify future areas of opportunities in physician wellness
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Health Care Workers
Arm Type
Experimental
Arm Description
Faculty, staff, and trainees dealing with COVID-19 pandemic
Intervention Type
Behavioral
Intervention Name(s)
Crisis management coaching
Intervention Description
Crisis management coaching will be offered to faculty, staff, and trainees dealing with COVID-19 pandemic
Primary Outcome Measure Information:
Title
Change in stress level as measured by survey
Time Frame
Baseline, mid-session (up to 4 weeks), post-intervention (up to 8 weeks)
Secondary Outcome Measure Information:
Title
Change wellness as measured by survey
Description
Survey is 14-items asking about wellness on a scale from "Strongly Agree" to "Not at all"
Time Frame
Baseline, mid-session (up to 4 weeks), post-intervention (up to 8 weeks)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Any faculty, staff, or trainee from Duke pulmonary and critical care that consents to being in the study
Exclusion Criteria:
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patty Lee, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sangeeta Joshi, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
COPING With COVID-19( CWC-19)
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