COPING With COVID-19( CWC-19)

Sponsor

Duke University (Other)

Overall Status

Withdrawn

CT.gov ID

NCT04343690

Collaborator

(none)

Enrollment

Location

Arm

1.1

Actual Duration (Months)

Patients Per Site Per Month

Study Details

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

Condition or Disease	Intervention/Treatment	Phase
COVID-19	Behavioral: Crisis management coaching	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Other

Official Title:

Effectiveness of Crisis Management Coaching on Faculty and Trainee Wellness During COVID-19 Crisis

Actual Study Start Date :

Mar 27, 2020

Actual Primary Completion Date :

May 1, 2020

Actual Study Completion Date :

May 1, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Health Care Workers Faculty, staff, and trainees dealing with COVID-19 pandemic	Behavioral: Crisis management coaching Crisis management coaching will be offered to faculty, staff, and trainees dealing with COVID-19 pandemic

Arm

Intervention/Treatment

Experimental: Health Care Workers

Faculty, staff, and trainees dealing with COVID-19 pandemic

Behavioral: Crisis management coaching

Crisis management coaching will be offered to faculty, staff, and trainees dealing with COVID-19 pandemic

Outcome Measures

Primary Outcome Measures

Change in stress level as measured by survey [Baseline, mid-session (up to 4 weeks), post-intervention (up to 8 weeks)]

Secondary Outcome Measures

Change wellness as measured by survey [Baseline, mid-session (up to 4 weeks), post-intervention (up to 8 weeks)]
Survey is 14-items asking about wellness on a scale from "Strongly Agree" to "Not at all"

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Any faculty, staff, or trainee from Duke pulmonary and critical care that consents to being in the study

Exclusion Criteria:

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Duke University	Durham	North Carolina	United States	27710

Sponsors and Collaborators

Duke University

Investigators

Principal Investigator: Patty Lee, MD, Duke University
Principal Investigator: Sangeeta Joshi, MD, Duke University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Duke University

ClinicalTrials.gov Identifier:

NCT04343690

Other Study ID Numbers:

Pro00105319

First Posted:

Apr 13, 2020

Last Update Posted:

Sep 23, 2020

Last Verified:

Apr 1, 2020

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

COVID-19

Study Results

No Results Posted as of Sep 23, 2020