Verdes Montenegro Atalaya 2021.
Study characteristics | ||
Methods |
Study design: cluster‐randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Experimental group 1: MRBS 4 weeks
Experimental group 1: MRBS 8 weeks
Control: no intervention
Overall
Included criteria: NR Excluded criteria: NR Pretreatment: At baseline, statistically significant differences were found between the three groups in age, professional type, and work experience. Compliance rate: NR Response rate: NR Type of healthcare worker: various types of healthcare workers |
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Interventions |
Intervention characteristics Experimental group 1: MRBS 4 weeks
Experimental group 1: MRBS 8 weeks
Control: no intervention
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Outcomes | PSQ
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Identification |
Sponsorship source: NR Country: Spain Setting: Spanish National Health System teaching units Comments: NR Authors name: Juan Carlos Verdes‐Montenegro‐Atalaya Institution: Family and Community Medicine Teaching Department of Burgos, 0 Email: juancarlosverdesm@yahoo.es Address: Family and Community Medicine Teaching Department of Burgos, 09006 Burgos, Spain Time period: NR |
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Notes | PHQ included in analysis 1.1. Intervention groups combined to create a single pair‐wise comparison | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "Each TU was considered as a different and independent cluster, randomly assigned to the CG (2 TUs) or one of the two EGs (4 TUs)." Insufficiently described. |
Allocation concealment (selection bias) | Unclear risk | Quote: "EG1 participants were included in a standard training program of mindfulness and self‐compassion; while EG2, in an abbreviated one. Furthermore, the participants from each TU were stratified according to the type of professional (66 tutors versus 66 resident intern specialists)." 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 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 | 53 of the 165 (32%) randomised participants lost to follow‐up. Reasons provided. The baseline characteristics of participants who dropped out of the study were similar to those who completed it, so systematic selectionbias is unlikely. |
Selective reporting (reporting bias) | Unclear risk | No trial registration or no study protocol reported nor did we find one online |
Other bias | Unclear risk | Statistically significant differences were observed between the three groups in age, type of professional, and time working in the Spanish National Health System |