- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT04808635
The Predictors of Depression and Burnout Among Surgical Residents: A Cross-sectional Study From Kuwait
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
-
-
Outside U.S./Canada
-
Kuwait, Outside U.S./Canada, Kuwait, 00000
- Mubarak Al Kabeer hospital
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
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.
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
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
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Symptoms of depression were assessed using the 9-item Patient Health Questionnaire (PHQ-9) score
Tidsram: 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)
Tidsram: 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
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- MOHKWMKH21
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-delning som stöder informationstyp
- STUDY_PROTOCOL
- SAV
- ICF
- ANALYTIC_CODE
- CSR
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .