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Clinical Trials/NCT02512198
NCT02512198
Completed
Not Applicable

Electronic Prescription Data to Improve Primary Care Prescribing

University of Dundee1 site in 1 country236 target enrollmentJuly 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physician's Practice Patterns
Sponsor
University of Dundee
Enrollment
236
Locations
1
Primary Endpoint
Number of people identified by the measures of high risk or low quality prescribing
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This is a randomised controlled study to evaluate the effect of providing prescribing feedback that includes individual patient data to General Practitioners (GP) in Scotland on high risk or low quality prescribing.

Detailed Description

This study makes use of data held in the Prescription Information System (PIS), the national database available to national health service (NHS) health boards in Scotland, on all prescriptions dispensed by community pharmacists which include the unique patient identifier for Scotland (CHI). The design is a two parallel arm cluster randomised trial with general practices as the unit of randomisation to whom the feedback intervention is directed, and outcomes measured at patient level. Both arms receive the same active interventions but focused on different topics, with each acting as control to the other. The primary outcome in the asthma arm is a composite of measure of potentially high-risk asthma prescribing (multiple short acting beta-agonists or single agent long acting beta-agonists both in the absence of inhaled corticosteroid therapy). The primary outcome in the urinary tract infection antibiotic arm is a measure of repeated use of single (likely long-term prevention) or multiple (repeated treatment courses) urinary tract infection antibiotics. Within the feedback, alongside the patient-level analysis, there will be action-orientated messages to guide the GP practice. GP practices will get the reports three times at six-monthly intervals.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
July 1, 2017
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • GP practices in the participating Health Board area (NHS Greater Glasgow and Clyde)

Exclusion Criteria

  • GP practices with registered list sizes \<250 patients (all of these are unusual practices in various ways, for example serving the homeless or people with challenging behaviour).
  • GP practices with \<80% of prescriptions for inhaled bronchodilators and UTI antibiotics in the prescription database with a recorded patient identifier for each month from January 2014 to December
  • GP practices which were created after 1 January 2015.

Outcomes

Primary Outcomes

Number of people identified by the measures of high risk or low quality prescribing

Time Frame: 12 months

Secondary Outcomes

  • Cost-effectiveness of feedback(12 months)

Study Sites (1)

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