Study of Whether Educational Visits to Primary Care Professionals Improves the Quality of Care They Provide.
NCT ID: NCT00393536
Last Updated: 2006-10-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
73 participants
INTERVENTIONAL
1999-07-31
2000-12-31
Brief Summary
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Detailed Description
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In 1996, the then Newcastle and North Tyneside Health Authority established a Clinical Effectiveness Unit. The remit of the Unit was to provide support to local health care teams in primary and secondary care, with the aim of promoting clinical effectiveness and encouraging the use of best evidence in daily practice through systematic, evidence-based approaches to guideline implementation. The strategy adopted by the Clinical Effectiveness Unit was to concentrate on five clinical areas. These were selected by a multi-disciplinary steering group using explicit criteria (evidence of inappropriate variation in practice; a good evidence base for what should be done; the clinical area should be a source of significant morbidity or mortality; large cost implications in the management of the topic). Depression was one of the clinical areas chosen.
The aim of this study was, for the choice of antidepressants for the management of depression, to evaluate, within a pragmatic cluster randomized controlled trial, the effectiveness of outreach visiting by existing Pharmaceutical Advisers in addition to the postal distribution of educational materials.
Methods Within a pragmatic randomized controlled trial, involving all general practices in two PCTs, routine methods were used to distribute guidelines for the choice of antidepressants for the management of depression. Intervention practices were offered two visits (most accepted only one) by their PCT Pharmaceutical Adviser who had been trained in the techniques of outreach visiting. The intervention was evaluated using level three Prescribing Analysis and Cost (PACT) data for antidepressant drugs for the six months during which the intervention was delivered and the subsequent 12 months
Conditions
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Keywords
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Study Design
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RANDOMIZED
SINGLE_GROUP
HEALTH_SERVICES_RESEARCH
NONE
Interventions
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Educational outreach visiting
Eligibility Criteria
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Inclusion Criteria
ALL
No
Sponsors
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Newcastle University
OTHER
Principal Investigators
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Martin P Eccles, MD
Role: PRINCIPAL_INVESTIGATOR
University of Newcastle Upon-Tyne
Locations
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Institute of Health and Society
Newcastle upon Tyne, Tyne and Wear, United Kingdom
Countries
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Other Identifiers
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UEOVPAPHC-01
Identifier Type: -
Identifier Source: org_study_id