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Table 5 Primary feasibility outcome

From: GloveCare: a pilot study in preparation for a cluster crossover randomized controlled trial of non-sterile glove-based care in preventing late-onset infection in the NICU

Outcome

Target

Results

Participant enrolment (N (%))

>90%

1005 (100%)

Event rate of LOI—number of patients (N (%))

Not applicable

75 (10%)

Adequacy of resource allocation

1 FTE Research coordinator

Required extra data entry support

Processing time for evaluating new LOS

Not applicable

Estimated at 5 to 30 min depending on complexity of LOI

Adjudication of LOS (mean (range))

Not applicable

20 minutes per case (3–45 min)

Accuracy of data collection

Not applicable

Adjudication resulted in exclusion of 124 LOIs

Hand hygiene compliance moment 1

>90% in both arms

87.03% in standard arm,

78.28% in GloveCare arm

Hand hygiene compliance moment 4

>90% in both arms

87.37% in standard arm

80.76% in GloveCare arm

Glove compliance moment 1

>90% in GloveCare arm

66.2% in GloveCare arm

Glove compliance moment 4

>90% in GloveCare arm

83.30% in GloveCare arm

  1. LOI late onset infection, LOS length of stay