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. 2023 Oct 24;2023(10):CD014722. doi: 10.1002/14651858.CD014722.pub2

Yusoff 2015.

Study characteristics
Methods Study design: RCT
Duration of study: the study was published in 2014.
Country: Malaysia
Income classification: upper‐middle‐income country from 1992
Geographical scope: not specified
Healthcare setting: university (medical school)
Participants 1. Age: not specified (adults)
2. Gender: both
3. Socioeconomic background: not specified
4. Educational background: medical students from each year of study (mainly in first academic year accepted)
Inclusion criteria:
a. medical students from each year of study;
b. attend a 3‐h briefing session on the study protocol;
c. signed informed consent form.
Exclusion criteria:
no exclusion criteria.
Note: at baseline, the intervention and control group scores for Beck’s Depression Inventory (BDI) were, respectively, 5.55 (4.98) and 4.56 (4.66).
Stated purpose: to evaluate the effectiveness of a DEAL‐based based intervention on medical students' depression symptoms, coping strategies, and perceived stressors
Interventions Name: DEAL‐based intervention
Title/name of PW and number: medical teachers
1. Selection: not specified
2. Educational background: not specified
3. Training: it did not require any special training.
4. Supervision: not specified
5. Incentives/remuneration: not specified
Prevention type: universal prevention – all participants were eligible for inclusion, and their baseline scores for the BDI were well below the cut‐off for the measure.
Intervention details: the intervention is a 4‐hour educational workshop based on the DEAL model. It comprises four sections; the first section focuses on an introduction to the workshop and delivering information about stress, stressors, and coping strategies that are relevant to medical students (Section 1.0); the second section focuses on the practical aspects of self‐evaluation‐related stress, stressors and coping strategies (Section 2.0); the third section focuses on group work on dealing with stressful situations based on video clips (Section 3.0); the fourth section focuses on sharing experience, feedback, and conclusion about the whole activities (Section 4.0). Participants completed the intervention within 240 minutes (4 hours) over a half‐day.
Control: waiting list
Outcomes Participants’outcomes of interest for this review
  1. Depressive symptoms – BDI


Carers’outcomes of interest for this review
Nil
Economic outcomes
Nil
Time points: baseline, post‐intervention (< 1 month, 1‐6 months, 7‐24 months)
Notes Source of funding: University Sains Malaysia funding this study under the Research University Grant 1001/PPSP/812086
Notes on validation of instruments (screening and outcomes): BDI has been validated across regions, and the reliability coefficients (Cronbach’s alpha) have ranged from 0.76 to 0.95, with a mean of 0.86. Its uses have been validated in a nonpsychiatric sample. The measurement tool has been validated by previous studies in the Malaysian context.
Additional information: additional dataset available after request to the corresponding author
Handling the data: none
Prospective trial registration number: not available