Burnout Syndrome Among Medical Residents

September 11, 2018 updated by: matteo serenari, IRCCS Azienda Ospedaliero-Universitaria di Bologna
Whether and to what extent burnout risk is actually higher in surgical specialties than in non-surgical specialties is still unknown. Little is also known about what factors are associated with burnout between surgical residents and non-surgical residents. In this context, the present study has a three-fold aim: 1) to measure the prevalence of burnout among a sample of Italian medical residents; 2) to contrast the prevalence of burnout and psychological distress in surgical residents and non-surgical residents, and 3) to identify the work-related factors associated with burnout between surgical residents and non-surgical residents.

Study Overview

Status

Completed

Conditions

Detailed Description

Surgical training is considered to be very stressful among residents and graduating medical students choose less often surgery for their career. To elaborate burnout prevention programs, the assessment of the prevalence of burnout during the early career stage of the surgeons and associated risk factors, becomes central.

Residents from the University of Bologna were asked to participate in an anonymous online survey. The residents completed a set of questions regarding their training schedule and three standardized questionnaires: 1) the Maslach Burnout Inventory, assessing the three dimensions of burnout: emotional exhaustion (EE), depersonalization (DP), and personal accomplishment (PA); 2) the Zung Self-Rating Depression scale; 3) the Psychosomatic Problems scale. High scores in either the EE or DP subscale categories predicted professional burnout.

Study Type

Observational

Enrollment (Actual)

679

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • BO
      • Bologna, BO, Italy, 40100
        • University of Bologna

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.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All the residents attending the University of Bologna in the academic year 2017/2018

Description

Inclusion Criteria:

  • residents attending the University of Bologna

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
surgical residents
Surgical specialties included general surgery, plastic surgery, urology, vascular surgery, obstetrics and gynecology, orthopedic surgery, pediatric surgery, cardiothoracic surgery and otolaryngology.
non-surgical residents
Non-surgical specialties included cardiology, rheumatology, neurology, pulmonary disease, endocrinology, nuclear medicine, pediatrics, psychiatry, internal medicine, oncology, nephrology, hygiene and preventive medicine, anesthesiology, child and adolescent psychiatry, radiology, radiation oncology, infectious disease, dermatology, pathology, microbiology, hematology, gastroenterology, geriatric medicine, medical genetics, sports medicine, occupational and environmental medicine.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maslach Burnout Inventory
Time Frame: 3 months
a validated 22-item questionnaire that evaluates burnout in its three dimensions: emotional exhaustion (EE) depersonalization (DP) and personal accomplishment (PA). Responses are made on a 7-point Likert scale ranging from 0 ("never") to 6 ("daily").
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Zung Self-Rating Depression Scale
Time Frame: 3 months
The level of depressive symptoms was measured using the 20-item Zung Self-Rating Depression Scale. Items responses rank from 1 ("none or little of the time") to 4 ("most or all of the time"), and the total score range from 20 to 80 points. A score of 50 and above indicated the presence of at least mild-moderate depressive symptoms.
3 months
Psychosomatic Problems Scale
Time Frame: 3 months
Psychosomatic symptoms were measured using the Psychosomatic Problems Scale, which consists of 8 items: difficulty concentrating, sleep problems, headache, stomachache, tensions, lack of appetite, feeling sad, and dizziness. Responses are rated on a 5-point Likert scale, ranging from 1 ("never") to 5 ("always"). Participants answering "often" or "always" on an item are coded as having a psychosomatic symptom.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: antonio d pinna, MD, IRCCS Azienda Ospedaliero-Universitaria di Bologna

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 Major Dates

Study Start (ACTUAL)

October 16, 2017

Primary Completion (ACTUAL)

November 5, 2017

Study Completion (ACTUAL)

November 6, 2017

Study Registration Dates

First Submitted

September 9, 2018

First Submitted That Met QC Criteria

September 11, 2018

First Posted (ACTUAL)

September 12, 2018

Study Record Updates

Last Update Posted (ACTUAL)

September 12, 2018

Last Update Submitted That Met QC Criteria

September 11, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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