Ghawadra 2020.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Mindfulness‐based training
Control (no intervention)
Overall
Included criteria: nurses who work in wards who had mild to moderate levels of stress and depression (according to DASS‐21) in an earlier cross‐sectional survey. Excluded criteria: nurses who work in the outpatient clinic, or nursing managers, due to the different types of patient care, roles and responsibilities. Nurses who have a history of mental illness (n = 3) were excluded in the first study. The nurses who had severe and extremely severe levels of SAD (according to DASS‐21). They were advised to seek professional help at the psychiatric/psychology clinic in the hospital. Pretreatment: reported socio‐demographic baseline characteristics of participants randomised to the intervention group were similar to socio‐demographic baseline characteristics of participants randomized to the control group Compliance rate: the drop‐out rate was high, especially for the website intervention (48.3%). Response rate: it seems that all eligible participants actually participated Type of healthcare worker: nurses |
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Interventions |
Intervention characteristics Mindfulness‐based training
Control (no intervention)
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Outcomes |
DASS ‐ Depression
DASS ‐ Anxiety
DASS ‐ stress
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Identification |
Sponsorship source: NR Country: Malaysia Setting: Hospital Comments: NR Authors name: Sajed Faisal Ghawadra Institution: Department of Nursing Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysi Email: katlim@um.edu.my Address: Khatijah Lim Abdullah, Department of Nursing Science, Faculty of Medicine, University of Malaya, 506030 Kuala Lumpur, Malaysia and Fakultas Keperawatan Universitas Airlangga, Surabaya, Indonesia Time period: NR |
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Notes | Not able to include in analysis due to missing data. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "The participants were randomly assigned to the intervention and control groups using stratified blocked randomization." Sequence generation process insufficiently described. |
Allocation concealment (selection bias) | Unclear risk | Unable to judge whether participants and/or investigators could possibly 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 | 25 of the 249 (11%) participants were not analysed. Reasons provided. Not mentioned whether lost to follow‐up was at random however loss to follow‐up is below our pre‐defined cut‐off point. |
Selective reporting (reporting bias) | Unclear risk | Trial registration, nor did we find one online |
Other bias | Low risk | Low compliance but the per protocol analysis did not differ from the intention to treat analysis. Per‐protocol (PP) analysis was performed for (n = 136) participants who completed all the intervention (workshop and website), and for those who completed the three‐point questionnaires; the intervention and control group in PP analysis were n = 37 and 99, respectively. The results of the PP using GEE were similar to ITT, which strengthens the validity of the results |