An Analysis of Burnout Among Surgery Residents at a Tertiary Care Hospital in Pakistan: A Prospective Cohort Study

January 31, 2024 updated by: Mansoor Ahmed, Shaheed Zulfiqar Ali Bhutto Medical University

An Analysis of Burnout Among Surgery Residents at a Tertiary Care Hospital in Pakistan

To determine the scores of exhaustion, depersonalization and personal achievement according to Maslach Burnout Inventory (MBI) in surgical residents.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

A prospective cohort study was conducted at Pakistan Institute of Medical Sciences Islamabad with a 6-month duration from June 1, 2023 to November 30, 2023 after approval from the Institutional review board, 95 surgical residents working in Departments of Surgery & Allied of age less than 35 years (any gender) with duty of at least 60 hours per week were enrolled in study by using non-probability convenience sampling technique. Residents were informed about the study procedure and consent for inclusion was taken from them. Data analysis was done through SPSS v.26.

Study Type

Observational

Enrollment (Actual)

95

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

      • Islamabad, Pakistan, 44000
        • Shaheed Zulfiqar Ali Bhutto Medical University/PIMS

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Post graduate residents working in surgery and allied.

Description

Inclusion Criteria:

  • Residents working in departments of surgery and allied
  • Both genders
  • Less than 35 years old
  • Performing duty of at least 60 hours per week

Exclusion Criteria:

  • Those who did not wish to participate

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To determine the scores of exhaustion, depersonalization and personal achievement according to Maslach Burnout Inventory (MBI) in surgical residents.
Time Frame: 6 months

These components are added to get the total score. It is interpreted as given below:

A.Burnout i.≤ 17: Low-level burnout ii.18 to 29: Moderate burnout iii.> 30: High-level burnout B.Depersonalization i.≤ 5: Low-level burnout ii.6 to 11: Moderate burnout iii.≥ 12: High-level burnout C.Personal achievement i.≤ 33: High-level burnout ii.34-39: Moderate burnout iii.≥ 40: Low level burnout

6 months

Collaborators and Investigators

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

June 1, 2023

Primary Completion (Actual)

November 30, 2023

Study Completion (Actual)

November 30, 2023

Study Registration Dates

First Submitted

January 22, 2024

First Submitted That Met QC Criteria

January 22, 2024

First Posted (Actual)

January 31, 2024

Study Record Updates

Last Update Posted (Actual)

February 1, 2024

Last Update Submitted That Met QC Criteria

January 31, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • F.3-1/2023(ERRB)/Chairman

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Confidentiality

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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