Larson 2000.
Study characteristics | ||
Methods | Randomised controlled trial | |
Participants | 16 full‐time neonatal intensive care unit (NICU) nurses. Number of neonates not mentioned Inclusion criteria: nurses were selected for inclusion in the study because they represented stable and consistent staff and because approximately 70% of direct patient contacts on that unit were provided by nurses.
"Nurses were eligible to participate if they worked full time on day or night shift in the NICU, had no dermatologic conditions such as psoriasis or latex hypersensitivity, were not receiving topical or systemic steroids or antibiotics, were willing to be randomly assigned to one of 2 treatment groups and follow all study regimens, and had no holiday scheduled during the 4‐week study period". Exclusion criteria Not reported |
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Interventions |
Treatment group
Control group
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Outcomes |
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Notes | This study was supported in part by Steris Corporation, St Louis, MO. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | 16 nurses (8 per group) were randomly assigned by coin toss to 1 of 2 hand care regimens. |
Allocation concealment (selection bias) | High risk | It was not reported if allocation was concealed; probably not done |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No blinding, and 1 of the outcomes (self‐rating hand skin assessment) was likely to be influenced by lack of blinding. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not stated whether outcome assessors were blinded to the intervention |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All participants were accounted for. |
Selective reporting (reporting bias) | Low risk | All important outcomes were reported. |
Other bias | Low risk | None was suspected. |