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Nurse Promotion of IV to PO Antimicrobial Conversion

Not Applicable
Completed
Conditions
Behavior Change
Bacterial Infections
Interventions
Behavioral: Professional Behavior Change Intervention
Registration Number
NCT03761043
Lead Sponsor
Kelowna General Hospital
Brief Summary

This is a prospective, quasi-experimental, historically controlled study to evaluate if a behavioural change intervention informed by the COM-B model of behaviour change can improve nurses' self-perceived capability, opportunity, and motivation to engage in the assessment of patients who may be appropriate for IV to PO antimicrobial conversion. This study also seeks to determine if this translates into an increase in IV to PO antimicrobial conversion rates in the acute care setting.

Detailed Description

Current antimicrobial stewardship guidelines recommend appropriate and timely IV to PO antimicrobial conversion in hospitalized patients. Published rates of IV to PO antimicrobial conversion are consistently below 50% in eligible inpatients. Studies have suggested that nurses may be well positioned to provide a positive influence on prescriber behavior related to antimicrobial IV to PO conversion, however, no published research has evaluated the impact of nurses on antimicrobial IV to PO conversion rates. Published research has described the barriers and enablers to nurse participation in promoting antimicrobial IV to PO conversion using the COM-B model of behaviour change. This quasi-experimental study will evaluate whether determinants of nurse behaviour and their actual behaviour can be changed to increase antimicrobial IV to PO conversion rates in hospitalized patients.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
853
Inclusion Criteria
  • Nineteen years of age or older
  • Employed as a RN or LPN at KGH in any capacity (full-time, part-time or casual employee)
  • Practicing on a medicine/thoracic surgery ward (4A) or medicine/oncology/respiratory ward (4B)
Exclusion Criteria
  • RNs or LPNs on orientation shifts/training
  • RNs or LPNs not engaged in patient care
  • Student nurses/nurses in training

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Post-Intervention ArmProfessional Behavior Change InterventionThe nurses will have been exposed to the behavior change intervention.
Primary Outcome Measures
NameTimeMethod
IV to PO antimicrobial conversion rateSix months (three months pre-intervention, three months post-intervention)

Incidence of IV to PO antimicrobial conversion (defined as the initiation of a PO antimicrobial within 24 hours of discontinuation of an IV antimicrobial during a single treatment course in a specific patient) before and after behavior change intervention

Secondary Outcome Measures
NameTimeMethod
Days of IV therapy prior to conversion to PO antimicrobialSix months (three months pre-intervention, three months post-intervention)

For treatment courses that undergo IV to PO antimicrobial conversion, the days of IV antimicrobial therapy prior to PO conversion before and after intervention

Nurse perceptions of capability, opportunity and motivation to promote IV to PO antimicrobial conversionSix months (three months pre-intervention, three months post-intervention)

Constructs are derived using the Theoretical Domains Framework and assess nurse perceived capability, motivation, and opportunity to promote IV to PO antimicrobial conversion using a 7-point Likert scale (1 - Strongly Disagree, 2 - Disagree, 3- Slightly Disagree, 4 - Neither Agree or Disagree, 5 - Slightly Agree, 6 - Agree, 7- Strongly Agree). The average Likert scale score for each of nine constructs (based on the Theoretical Domains Framework) will be calculated for the pre-intervention period and the post-intervention period. Change in the average Likert score for each construct (question) in the pre-intervention period versus the post-intervention period will be compared for each construct. A higher average Likert score on a construct in the post-intervention period compared to the pre-intervention period indicates improved perceptions about capability, opportunity, or motivation to promote IV to PO antimicrobial conversion.

Trial Locations

Locations (1)

Kelowna General Hospital

🇨🇦

Kelowna, British Columbia, Canada

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