Huang 2020a.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Balint intervention
Wait‐list control group
Overall
Included criteria: NR Excluded criteria: NR Pretreatment: there were no significant differences between the two groups for age and gender Compliance rate: 100% Response rate: all residents invited voluntarily participated (100% response rate). Type of healthcare worker: residents |
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Interventions |
Intervention characteristics Balint intervention
Wait‐list control group
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Outcomes |
Maslach Burnout Inventory human services survey ‐ Emotional Exhaustion
Maslach Burnout Inventory human services survey ‐ Depersonalisation
Maslach Burnout Inventory human services survey ‐ Personal accomplishment
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Identification |
Sponsorship source: NR Country: China Setting: Hospital Comments: NR Authors name: Lei Huang Institution: Department of Psychiatry, Tongji Hospital, Tongji University School of Medicine, Shanghai, China, Medical Education Division, Tongji Hospital, Tongji University School of Medicine, Shanghai, China Email: wuwy@tongji.edu.cn Address: NR Time period: 2016 |
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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) | Unclear risk | Quote: "Following consent and the completion of the first round of assessment completion, the 36 residents were randomly assigned to the intervention (n = 18) or the control group (n = 18)." Sequence generation process insufficiently described |
Allocation concealment (selection bias) | Unclear risk | Difficult to judge whether participants and/or investigators could possible foresee assignment. However, it is assumed that randomization was performed in one go and that participants and/or investigators could not foresee assignment. |
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 | Low risk | No loss to follow‐up. |
Selective reporting (reporting bias) | Low risk | No trial registration or no study protocol reported. No indication of selective reporting. |
Other bias | Low risk | No indication of other sources of bias reported. |