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CompletedNCT03668080Updated Sep 12, 2018

Burnout Syndrome Among Medical Residents

An observational study in Burnout Syndrome, sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. Completed at 1 site in Italy. Per ClinicalTrials.gov, last updated 2018-09-12.

Sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
679
Sex
All
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Study summary

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.

Read the 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.

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Conditions studied

  • Burnout Syndrome

Keywords

  • burnout
  • residents
  • surgical residents
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In context

Syndrome

9,217 studies on the registry are indexed under Syndrome; 1,034 are open to participants now.

This study's enrollment of 679 is above the median of 102 across 2,211 observational studies indexed under Syndrome.

Browse Syndrome studies →

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna is the lead sponsor of 493 studies on the registry; 273 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

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

Inclusion criteria

  • residents attending the University of Bologna

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
679 participants (actual)
Patient registry
No

Groups and cohorts

  • 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.

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What researchers measure

Primary outcomes

  1. Maslach Burnout Inventory

    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").

    Time frame: 3 months

Secondary outcomes

  1. Zung Self-Rating Depression Scale

    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.

    Time frame: 3 months

  2. Psychosomatic Problems Scale

    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.

    Time frame: 3 months

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Study locations

1 site
  • University of Bologna
    Bologna, BO 40100, Italy
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References and documents

Publications

  • Maslach C, Schaufeli WB, Leiter MP. Job burnout. Annu Rev Psychol. 2001;52:397-422. doi: 10.1146/annurev.psych.52.1.397. PubMed 11148311 ↗
  • Serenari M, Cucchetti A, Russo PM, Fallani G, Mattarozzi K, Pinna AD, Colonnello V, Poggioli G, Cescon M. Burnout and psychological distress between surgical and non-surgical residents. Updates Surg. 2019 Jun;71(2):323-330. doi: 10.1007/s13304-019-00653-0. Epub 2019 Apr 2. PubMed 30941702 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 12, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03668080
Lead sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Responsible party
matteo serenari (Principal Investigator, IRCCS Azienda Ospedaliero-Universitaria di Bologna) — Principal investigator
First posted
Sep 12, 2018
Start date
Oct 16, 2017
Primary completion
Nov 5, 2017
Completion
Nov 6, 2017
Last update
Sep 12, 2018

Study contacts

antonio d pinna, MD
study director · IRCCS Azienda Ospedaliero-Universitaria di Bologna

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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