Lee 2020.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Psychotherapy
Control (no intervention)
Overall
Included criteria: the participant must be a practising physician of the primary healthcare system in Almaty (Kazakhstan), he/she should have at least one year of work experience; he/she must provide signed informed consent. Excluded criteria: incomplete filling out of questionnaires, refusal to participate in the study, lack of informed consent, dismissal from work. Pretreatment: according to the results, there was no statistically significant difference between age, gender, marital status and speciality of doctors in the two groups. Type of healthcare worker: exclusively doctors involved in primary healthcare Response rate: 93% Compliance rate: 23% |
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Interventions |
Intervention characteristics Psychotherapy
Control (no intervention)
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Outcomes |
Maslach Burnout Inventory ‐ Emotional Exhaustion
Maslach Burnout Inventory ‐ Depersonalisation
Maslach Burnout Inventory ‐ Personal accomplishment (lack of)
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Identification |
Sponsorship source: NR Country: Republic of Kazakhstan Setting: Two out‐patient‐clinics Comments: NR Authors name: Sergey Lee Institution: S.D. Asfendiyarov Kazakh National Medical University Email: lee.s.kaznmu@mail.ru Address: Tole Bi Street 94, Almaty, 050000, Kazakhstan Time period: 2019 |
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Notes | MBI‐EE included in analysis 1.2 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Participants were assigned with an individual number, after which they were randomized using online random tools (experimental and control groups into two groups): |
Allocation concealment (selection bias) | Unclear risk | Insufficient information to understand whether intervention allocations could have been foreseen in advance of, during, enrolment. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants were not blinded. |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Participants were not blinded whereas outcomes are self‐reported. |
Incomplete outcome data (attrition bias) All outcomes | High risk | 112 of the 243 randomised participants included in the analyses. Not reported whether lost to follow‐up was at random. |
Selective reporting (reporting bias) | Unclear risk | No trial protocol reported, nor did we find one online. |
Other bias | Low risk | No indication of other bias. |