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Clinical Trials/NCT03613441
NCT03613441
Completed
N/A

Impact of Mindful Awareness Practices in Pediatric Residency Training

University of California, Los Angeles1 site in 1 country82 target enrollmentJune 1, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stress
Sponsor
University of California, Los Angeles
Enrollment
82
Locations
1
Primary Endpoint
Change in level of stress per Perceived Stress Scale (PSS)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study evaluates the effect of a standardized mindfulness based intervention compared to control on self-reported levels of stress in residency trainees.

Detailed Description

Recent research studies have indicated that the practice of mindfulness is strongly correlated with enhanced well-being and improved resilience in a variety of populations. Mindfulness-based interventions have been shown to reduce stress and symptoms of burnout in physicians. However, the two studies that included residents were observational trials evaluating the effect of an abbreviated, informal mindfulness course. The aim of the investigator's study is to assess whether a standardized course in mindfulness meditation (Mindful Awareness Practices, MAPs) reduces self--reported signs and symptoms of stress, burnout, depression, anxiety, loneliness and poor sleep quality in residents in pediatrics training. This study is a randomized controlled trial using 2 parallel groups. The pediatrics residents randomized to the intervention will participate in a standardized mindful awareness practices intervention consisting of one live 45- minute session and 5 web--based self--study sessions. The live session will be administered by a trained mindfulness educator at the UCLA Westwood, Olive View Medical Center and Cedars--Sinai Medical Center campuses. The waitlist group will have the opportunity to participate in the same course once the study has been completed. Participants will respond to questionnaires to assess for levels of stress and other mental health measures before and after the intervention to see if the intervention group had a reduction in symptoms compared to the waitlist group.

Registry
clinicaltrials.gov
Start Date
June 1, 2017
End Date
April 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Denise Rita Purdie, MD, FAAP

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • Pediatric resident at the University of California Los Angeles's Mattel Children's Hospital
  • Medicine/Pediatric resident at University of California Los Angeles's Mattel Children's Hospital

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in level of stress per Perceived Stress Scale (PSS)

Time Frame: Baseline and at 2 months (immediately post-intervention)

PSS = validated 14-item self-report questionnaire of stress experienced over past month. Scores range from 0-56. Higher scores represent a worse outcome.

Secondary Outcomes

  • Change in symptoms of burnout per Abbreviated Maslach Burnout Inventory-9(Baseline and at 2 months (immediately post-intervention))
  • Change in symptoms of depression per Beck Depression Inventory (BDI)(Baseline and at 2 months (immediately post-intervention))
  • Change in symptoms of anxiety per Beck Anxiety Inventory (BAI)(Baseline and at 2 months (immediately post-intervention))
  • Change in level of loneliness per UCLA Loneliness Scale(Baseline and at 2 months (immediately post-intervention))
  • Change in level of sleep quality per Pittsburgh Sleep Quality Index (PSQI)(Baseline and at 2 months (immediately post-intervention))
  • Change in level of mindfulness per Mindful Attention Awareness Scale (MAAS)(Baseline and at 2 months (immediately post-intervention))

Study Sites (1)

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