- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06233669
An Analysis of Burnout Among Surgery Residents at a Tertiary Care Hospital in Pakistan: A Prospective Cohort Study
An Analysis of Burnout Among Surgery Residents at a Tertiary Care Hospital in Pakistan
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Islamabad, Pakistan, 44000
- Shaheed Zulfiqar Ali Bhutto Medical University/PIMS
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- F.3-1/2023(ERRB)/Chairman
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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