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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04584268
Other study ID # 201904014
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2019
Est. completion date July 20, 2020

Study information

Verified date October 2020
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This was a single-site RCT to assess the effect of a longitudinal mindfulness intervention on burnout for first-year (PGY-1) internal medicine (IM) and pediatrics residents. The primary outcome was Maslach Burnout Inventory MBI) scores at baseline and 12 month follow-up. Secondary outcomes were feasibility and perceived benefit of the intervention.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date July 20, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Washington University (WUSM) first year residents in internal medicine and pediatrics

Exclusion Criteria:

- none

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
mindfulness
in person and smart phone application mindfulness practice
Other:
standard medical education
standard medical education / control

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maslach Burnout Inventory (MBI) burnout score on MBI (score range 0-132); based on three components: emotional exhaustion, depersonalization, and personal accomplishment) 1 year
Primary feasibility of intervention in graduate medical education ability to insert into the curriculum without barriers or disruption of other education activities, assessed by interviews from residency leadership 1 year
Secondary evaluation of intervention survey to assess opinion of intervention (Likert scale) 1 year
Secondary effect on mindfulness practice survey question to assess pre and post-intervention frequency of practicing mindfulness 1 year
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