Medisauskaite 2019.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline Characteristics Interventions about the psychology of burnout, stress, coping with patient death, and managing distress
Control (no intervention)
Overall
Included criteria: doctors who currently practice medicine, have regular contact with patients Excluded criteria: NR Pretreatment: there were no significant differences between the two trial groups at baseline Type of healthcare worker: exclusively doctors Response rate: 89% Compliance rate: 78% |
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Interventions |
Intervention characteristics Interventions about the psychology of burnout, stress, coping with patient death, and managing distress
Control (no intervention)
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Outcomes |
Maslach Burnout Inventory ‐ Emotional exhaustion
Maslach Burnout Inventory ‐ Depersonalisation
Maslach Burnout Inventory ‐ Personal accomplishment
General Anxiety Disorder
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Identification |
Sponsorship source: The RCT was not funded or determined by Focus Games or any organization involved with the app/board game. Country: United Kingdom Setting: Among nine randomly selected NHS trusts, 9 royal colleges of medicine, and the British Medical Association (BMA) Comments: NR Authors name: Asta Medisauskaite Institution: Research Department of Medical Education Email: a.medisauskaite@ucl.ac.uk Address: UCL Medical School Room GF/644, Royal Free Hospital, NW3 2PF. Time period: From July to November 2016 |
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Notes | MBI‐EE included in analysis 1.1. GAD included in analysis 1.4. |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "Qualtrics software randomly assigned doctors to one of 5 trial groups:" |
Allocation concealment (selection bias) | Low risk | Quote: "Blindly to the researchers, Qualtrics software randomly assigned doctors to one of 5 trial groups:" |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Quote: "doctors were randomly and blindly assigned to one of 5 trial groups." |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Quote: "The trial group was manipulated between‐subjects such that doctors were randomly and blindly assigned to one of 5 trial groups." Outcomes are self‐reported. |
Incomplete outcome data (attrition bias) All outcomes | High risk | Quote: "2.2.4. Sample" Loss to follow‐up: 25% intervention; 27% control |
Selective reporting (reporting bias) | Unclear risk | No trial registration, nor did we find one online. |
Other bias | Low risk | No indication of other bias. |