Mache 2016.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Self‐care health intervention programme
Control (no intervention)
Overall
Included criteria: study participation requires positive inclusion criteria: (1) employment as a psychiatrist in a psychiatric department, (2) working full time, (3) being able and willing to take part in the study, (4) agreement to complete a survey at least three times. Excluded criteria: NR Pretreatment: only small, insignificant differences between intervention and control group have been found in baseline data on gender, age and working experience. Statistically significant positive advance was found for perceived stress, resilience and self‐efficacy in the intervention group. Type of healthcare worker: exclusively physicians Response rate: 51% Compliance rate: 95% |
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Interventions |
Intervention characteristics Self‐care health intervention programme
Control (no intervention)
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Outcomes |
Perceived Stress Questionnaire (PSQ)
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Identification |
Sponsorship source: NR Country: Germany Setting: Twelve hospital departments in the North of Germany specialising in Psychiatry Medicine Comments: NR Authors name: Stefanie Mache Institution: Institute for Occupational and Maritime Medicine (ZfAM), University Medical Center Hamburg‐Eppendorf Email: s.mache@uke.de Address: Seewartenstrasse 10, 20459 Hamburg, Germany Time period: NR |
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Notes | PSQ included in analysis 1.1 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "study. These physicians were randomised into two groups through a computer‐generated algorithm." |
Allocation concealment (selection bias) | Unclear risk | Quote: "The surveys were conducted by using a secure web‐based survey sys tem, via links within e‐mail messages." |
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 | Quote: "76 participants; four needed to be excluded due to health reasons (sickness absence)." Loss to follow‐up below our review's pre‐defined cut‐off value. |
Selective reporting (reporting bias) | Unclear risk | No trial registration, nor did we find one online. |
Other bias | Low risk | No indication of other bias. |