Developing and Evaluating Interventions to Reduce Inappropriate Prescribing of Antibiotics in Primary Care

NCT01206738 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2017-06-02

Study results available
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Summary

1. Do paper-based and web-based intervention modelling experiments (the methodology we are developing) identify the same predictors of GP behaviour regarding prescribing of antibiotics for upper respiratory tract infections?
2. Can a web-based IME system provide trialists with richer and more predictive information upon which to base the development of behavioural change interventions than paper-based IME systems?

Conditions

  • Antibiotic Prescribing by GPs for URTI

Interventions

BEHAVIORAL

Persuasive communication

The persuasive intervention aimed to reinforce the GP's beliefs about the positive consequences of managing sore throat without prescribing antibiotics.

BEHAVIORAL

Action plan

This intervention was an action plan, supporting the GP to deal with two difficult prescribing situations: 1) a distressed patient (or often distressed parent of a child patient) 2) a patient demanding an antibiotic

BEHAVIORAL

General intervention

No additional information was provided; the general information was the information already available to GPs about antibiotic prescribing.

Sponsors & Collaborators

  • University of Aberdeen

    collaborator OTHER
  • Newcastle University

    collaborator OTHER
  • University of Southampton

    collaborator OTHER
  • Chief Scientist Office of the Scottish Government

    collaborator OTHER_GOV
  • Scottish Primary Care Research Network

    collaborator UNKNOWN
  • Scottish School of Primary Care

    collaborator UNKNOWN
  • University of Dundee

    lead OTHER

Principal Investigators

  • Shaun Treweek, PhD · University of Dundee

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2012-05-31
Completion
2012-09-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01206738 on ClinicalTrials.gov