RECRUITING

Creative Arts Program to Reduce Burnout in Healthcare Professionals

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study plans to learn if creative arts programs that include visual, musical, written, or physical expression can reduce symptoms of burnout syndrome, Post Traumatic Stress Disorder (PTSD), depression, and anxiety in critical care healthcare professionals. This study also explores if creative arts can enhance the connection to the purpose of work, the development of adequate coping skills, while providing time to connect with peers.

Official Title

Creative Arts Program to Reduce Burnout in Healthcare Professionals

Quick Facts

Study Start:2020-03-01
Study Completion:2025-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04276922

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Employed as a healthcare provider, practicing primarily in a hospital setting for at least 20 hours per week.
  2. * Positive symptoms of burnout measured via the Maslach Burnout Inventory (MBI):
  3. * emotional exhaustion score of \>17, or
  4. * depersonalization score of \>7, or
  5. * personal accomplishment score of \< 31.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Kristen Torres, BS
CONTACT
303-724-6377
kristen.torres@cuanschutz.edu
Jeffrey McKeehan, MSN
CONTACT
303-724-6080
jeffrey.mckeehan@cuanschutz.edu

Principal Investigator

Marc Moss, MD
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of Colorado - Anschutz Medical Campus
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Marc Moss, MD, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-03-01
Study Completion Date2025-04-30

Study Record Updates

Study Start Date2020-03-01
Study Completion Date2025-04-30

Terms related to this study

Additional Relevant MeSH Terms

  • Burn-Out Syndrome
  • Post-Traumatic Stress Disorder
  • Depression, Anxiety