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Clinical Trials/NCT02825004
NCT02825004CompletedNot Applicable

Recognizing and Preventing Burnout: A Pilot Randomized Controlled Trial

Fondazione Don Carlo Gnocchi Onlus1 site in 1 country20 target enrollmentStarted: June 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
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)

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Control Group

No Intervention

There is not any intervention.

Psychological Intervention

Experimental

All the professionals workers involved in the experimental group will attend three intensive psychological meetings about emotional exhaustion, depersonalisation, low personal accomplishment and how to improve coping skills.

Intervention: Psychological Intervention (Behavioral)

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))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Paolo Banfi

M.D.

Fondazione Don Carlo Gnocchi Onlus

Study Sites (1)

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