Emotional Experience and Burnout in Physician (ETRE)

September 14, 2016 updated by: Assistance Publique - Hôpitaux de Paris

National Study of the Psychological Consequences Resulting From the Practice of Invasive Therapeutic Interventions: Mixed Evaluation, Qualitative and Quantitative, of Burn Out Among Digestive Surgeons, Gastroenterologists and Radiologists

Recent studies have highlighted a high incidence of burnout among surgeons. The aim of this study is in particular to investigate if this is the consequence of performing surgery (i.e. invasive procedures) or whether it is related to the cultural background of surgeons.

Study Overview

Status

Unknown

Conditions

Detailed Description

A mixed method approach (qualitative approach and quantitative approach) will be used to investigate surgeons, as well as gastroenterologists and radiologists who perform invasive procedures and gastroenterologists and radiologists who do not perform invasive procedures. The qualitative approach will rely on face-to face interviews with purposively sampled physicians of the 5 groups and will be continued until saturation. The quantitative approach will rely on a questionnaire that will be sent to physicians of the 5 groups.

Study Type

Observational

Enrollment (Anticipated)

3390

Contacts and Locations

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

Study Contact

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Digestive surgeon, Gastroenterologist, Radiologist

Description

Inclusion Criteria:

  • Digestive surgeon, Gastroenterologist, Radiologist

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
incidence of burnout
Time Frame: quantitative approach 27 months
Compare the emotional experience and incidence of burnout between surgeons, gastroenterologists and radiologists
quantitative approach 27 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
physicians understanding of the Maslach Burnout Inventory (MBI) questionnaire will be reported by interview
Time Frame: quantitative approach 27 months
quantitative approach 27 months
physician's emotions will be reported by interview and MBI questionnaire
Time Frame: quantitative approach 27 months
concordance between the questionnaire and the interview
quantitative approach 27 months
Correlation score depending on the specialty and professional experience
Time Frame: quantitative approach 27 months
Evaluation of the MBI score over time
quantitative approach 27 months

Collaborators and Investigators

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

Sponsor

Assistance Publique - Hôpitaux de Paris

Investigators

  • Principal Investigator: Olivier Farges, MD, PhD, Assistance Publique - Hôpitaux de Paris

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.

General Publications

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

October 1, 2016

Primary Completion (Anticipated)

December 1, 2018

Study Completion (Anticipated)

April 1, 2019

Study Registration Dates

First Submitted

August 25, 2016

First Submitted That Met QC Criteria

September 1, 2016

First Posted (Estimate)

September 8, 2016

Study Record Updates

Last Update Posted (Estimate)

September 15, 2016

Last Update Submitted That Met QC Criteria

September 14, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PHRQ14591

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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