- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04808635
The Predictors of Depression and Burnout Among Surgical Residents: A Cross-sectional Study From Kuwait
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a questionnaire based cross-sectional study conducted in Kuwait from jan 2021- February 2021 An online questionnaire was sent to the residents enrolled to the surgical residency programs in Kuwait. Residency training in Kuwait provides programs in both medical and surgical specialties. Specialties included in our cohort were: general surgery, orthopedic surgery, urology, neurosurgery, Obstetrics and Gynecology and otolaryngology.
The email sent to our participants included an invitation letter detailing the reason behind the questionnaire and that it is confidential and anonymous. Consent was obtained from participants.
Variables:
Variables collected included; age, gender, marital status, smoking history, exercise, specialty, year of training, on-call frequency, assessment of burnout and assessment of depression symptoms.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Outside U.S./Canada
-
Kuwait, Outside U.S./Canada, Kuwait, 00000
- Mubarak Al Kabeer hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- residents enrolled in surgical training in Kuwait. Across all surgical specialties From R1-R5
Exclusion Criteria:
Recently accepted candidates that have not yet started residency.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
general surgery residents
|
no intervention, this is an observational cross sectional study
|
orthopedic surgery residents
|
no intervention, this is an observational cross sectional study
|
urology residents
|
no intervention, this is an observational cross sectional study
|
OBGYN residents
|
no intervention, this is an observational cross sectional study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Symptoms of depression were assessed using the 9-item Patient Health Questionnaire (PHQ-9) score
Time Frame: 1 month
|
(PHQ-9) score, a self-report questionnaire that is commonly used as a screening tool for depression.
It is composed of 9 questions assessing the frequency of depressive symptoms on a 4-point Liker-scale ranging from 0 (never) to 3 (nearly every day).
The total score was calculated for each patient and was interpreted as follows: minimal (1-4), mild (5-9), moderate (10-14), moderately severe (15-21), severe (20-27).
A standard cutoff of score of 10 was used, indicating a diagnosis of depression.
|
1 month
|
Burnout symptoms were assessed using 9-item form of the Maslach Burnout Inventory - Human Services Survey (aMBI-HSS)
Time Frame: 1 month
|
The aMBI is a 9-item questionnaire each question is rated on a 7-point Liker scale ranging from 0 to 6, which indicates the frequency of symptoms in question.
Response options include; Every day, A few times a week, Once a week, A few times a month, Once a month, A few times a year, or Never.
The questions grouped into 3 subscales (emotional exhaustion EE, depersonalization D and personal accomplishment PA) are evaluated and scored separately with each score ranging from 0 to 18.
We used the cut off points set by Lebares et al. for EE and D. The cut off points for high burnout among U.S. surgery residents were: EE score ≥ 9 and D score ≥ 6.
A PA score ≤ 12 was chosen as a cut-off for high burnout.
|
1 month
|
Collaborators and Investigators
Sponsor
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
- MOHKWMKH21
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
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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