Amutio 2015.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Mindfulness training
Control (wait list)
Overall
Included criteria: willingness to complete the questionnaires and commitment to adhere to the programmes' attendance and dedication requirements. Excluded criteria: were being in psychiatric or psychological treatment, or not being actively practising at the time of the study. Pretreatment: no initial differences between groups were found for the main variables of our study (mindfulness, F = 2.51, P = 0.12; burnout, F = 1.11, P = 0.30; and emotional exhaustion, F = 2.87, P = 0.10), including demographic or professional characteristics (P > 0.05) Type of healthcare worker: exclusively physicians Response rate: NR Compliance rate: regarding acceptability of the intervention to participants, the attendance rates for the two phases of the program were 88% for weekly sessions and 72% for monthly sessions |
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Interventions |
Intervention characteristics Mindfulness training
Control (wait list)
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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: The authors report the University of the Basque Country (UPV/EHU)provided funding for the materials and travel expenses. The Official Medical College of Biscay in Spain provided the physical setting to conduct the sessions. Country: Spain Setting: all participants were actively used in public (42.9%) or private (52.4%) practice. Comments: NR Authors name: Alberto Amutio, PhD; Institution: Department of Social Psychology and Methodology of the BehavioralSciences, Faculty of Psychology, University of the Basque Country (UPV/EHU), Spain Email: Alberto.amutio@ehu.eus Address: Avda Tolosa, 70, Donostia‐San Sebastian, Gipuzko Time period: NR |
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Notes | MBI‐EE included in analysis 1.1 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "Participants in the experimental group (n = 21) were randomly selected using the statistical program SPSS 20.0. The remaining subjects were included in the control group (n = 21)." |
Allocation concealment (selection bias) | Unclear risk | Judgement Comment: Unable to judge whether participants and/or investigators could possibly foresee assignment |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Quote: "Each participant in the experimental group committed to attending the sessions, doing the exercises assigned as home‐work, and answering the evaluation questions at the end of each of the phases of the study. The waitlist control group was told that a similar course would be offered again." Judgement Comment: 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 | Unclear risk | not explicitly stated whether participants dropped out. |
Selective reporting (reporting bias) | Unclear risk | No trial registration or no study protocol reported, nor did we find one online. |
Other bias | Low risk | No indication of other sources of bias |