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Clinical Trials/NCT02825004
NCT02825004
Completed
Not Applicable

Recognizing and Preventing Burnout: A Pilot Randomized Controlled Trial

Fondazione Don Carlo Gnocchi Onlus1 site in 1 country20 target enrollmentJune 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Burnout, Professionals
Sponsor
Fondazione Don Carlo Gnocchi Onlus
Enrollment
20
Locations
1
Primary Endpoint
Changes in burnout, as assessed by the Maslach Burnout Inventory (MBI) (Maslach C., 1981) between baseline (T0), 6 months (T1) and 12 months (T2)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to prevent burnout and offer the hospital staff a space for processing the emotional experiences.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
January 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paolo Banfi

M.D.

Fondazione Don Carlo Gnocchi Onlus

Eligibility Criteria

Inclusion Criteria

  • Doctors, physiotherapists, nurses and care workers
  • Be a Professional Worker at the Rehabilitation Respiratory Unit
  • Age \> 18 years old

Exclusion Criteria

  • Refusal at the Informed Consent

Outcomes

Primary Outcomes

Changes in burnout, as assessed by the Maslach Burnout Inventory (MBI) (Maslach C., 1981) between baseline (T0), 6 months (T1) and 12 months (T2)

Time Frame: At the baseline (T0), 6 months (T1) and 12 months (T2)

Secondary Outcomes

  • Changes in psychological symptoms as assessed by the Symptom Checklist-90-R (Prunas et al., 2012) between baseline (T0), 6 months (T1) and 12 months (T2)(At the baseline (T0), 6 months (T1) and 12 months (T2))
  • Changes in coping strategies as assessed by the Coping Orientation to Problems Experienced (COPE) (Carver et al., 1989) between baseline (T0), 6 months (T1) and 12 months (T2)(At the baseline (T0), 6 months (T1) and 12 months (T2))

Study Sites (1)

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