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Recognizing and Preventing Burnout

Primary Purpose

Burnout, Professionals

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Psychological Intervention
Sponsored by
Fondazione Don Carlo Gnocchi Onlus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Burnout, Professionals focused on measuring Burnout, Health Care Workers, Coping Skills, Clinical Trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Paolo Banfi

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Psychological Intervention

Control Group

Arm Description

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.

There is not any intervention.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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)
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)

Full Information

First Posted
July 4, 2016
Last Updated
January 31, 2018
Sponsor
Fondazione Don Carlo Gnocchi Onlus
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1. Study Identification

Unique Protocol Identification Number
NCT02825004
Brief Title
Recognizing and Preventing Burnout
Official Title
Recognizing and Preventing Burnout: A Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
August 2017 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Don Carlo Gnocchi Onlus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Professionals
Keywords
Burnout, Health Care Workers, Coping Skills, Clinical Trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Psychological Intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
There is not any intervention.
Intervention Type
Behavioral
Intervention Name(s)
Psychological Intervention
Primary Outcome Measure Information:
Title
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 Outcome Measure Information:
Title
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)
Time Frame
At the baseline (T0), 6 months (T1) and 12 months (T2)
Title
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)
Time Frame
At the baseline (T0), 6 months (T1) and 12 months (T2)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Facility Information:
Facility Name
Paolo Banfi
City
Milan
ZIP/Postal Code
20148
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
21334861
Citation
Prunas A, Sarno I, Preti E, Madeddu F, Perugini M. Psychometric properties of the Italian version of the SCL-90-R: a study on a large community sample. Eur Psychiatry. 2012 Nov;27(8):591-7. doi: 10.1016/j.eurpsy.2010.12.006. Epub 2011 Feb 21.
Results Reference
result
PubMed Identifier
23356679
Citation
Kleijweg JH, Verbraak MJ, Van Dijk MK. The clinical utility of the Maslach Burnout Inventory in a clinical population. Psychol Assess. 2013 Jun;25(2):435-41. doi: 10.1037/a0031334. Epub 2013 Jan 28.
Results Reference
result
PubMed Identifier
2926629
Citation
Carver CS, Scheier MF, Weintraub JK. Assessing coping strategies: a theoretically based approach. J Pers Soc Psychol. 1989 Feb;56(2):267-83. doi: 10.1037//0022-3514.56.2.267.
Results Reference
result

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Recognizing and Preventing Burnout

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