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MEDUCATE trial: effectiveness of an intensive EDUCATional intervention for IT-mediated MEDication management in the outpatient clinic - study protocol for a cluster randomized controlled trial.
van Stiphout, F; Zwart-van Rijkom, J E F; Aarts, J E C M; Koffijberg, H; Klarenbeek-deJonge, E; Krulder, M; Roes, K C B; Egberts, A C G; ter Braak, E W M T.
Afiliación
  • van Stiphout F; Department of Internal Medicine and Centre for Research and Development of Education, University Medical Centre Utrecht, the Netherlands, Hijmans van den Berghgebouw kamer 4.21, Huispostnummer HB 4.05, Postbus 85500, 3508, GA, Utrecht, The Netherlands. f.vanstiphout@umcutrecht.nl.
  • Zwart-van Rijkom JE; Department of Clinical Pharmacy, University Medical Centre Utrecht, Heidelberglaan 100, 3584, CX, Utrecht, The Netherlands. j.e.f.zwart-2@umcutrecht.nl.
  • Aarts JE; Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, PO Box 80082, 3508, TB, Utrecht, The Netherlands. j.e.f.zwart-2@umcutrecht.nl.
  • Koffijberg H; Institute of Health Policy and Management, Erasmus University Rotterdam, Rotterdam, The Netherlands. jaarts@buffalo.edu.
  • Klarenbeek-deJonge E; Department of Biomedical Informatics, School of Medicine and Biomedical Sciences, University at Buffalo, Roosevelt Hall, 923 Main Street, Buffalo, NY, 14203, USA. jaarts@buffalo.edu.
  • Krulder M; Department of Health Technology Assessment, Julius Center, University Medical Centre Utrecht, Utrecht, The Netherlands. h.koffijberg@umcutrecht.nl.
  • Roes KC; Faculty of Medicine, Utrecht University, Universiteitsweg 98, 3584, CG, Utrecht, The Netherlands. e.n.dejonge@umcutrecht.nl.
  • Egberts AC; Faculty of Medicine, Utrecht University, Universiteitsweg 98, 3584, CG, Utrecht, The Netherlands. merelkrulder@hotmail.com.
  • ter Braak EW; Department of Quality and Patient Safety, University Medical Centre Utrecht, Utrecht, The Netherlands. k.c.b.roes@umcutrecht.nl.
Trials ; 16: 223, 2015 May 22.
Article en En | MEDLINE | ID: mdl-25997633
ABSTRACT

BACKGROUND:

Using information technology for medication management is an opportunity to help physicians to improve the quality of their documentation and communication and ultimately to improve patient care and patient safety. Physician education is necessary to take full advantage of information technology systems. In this trial, we seek to determine the effectiveness of an intensive educational intervention compared with the standard approach in improving information technology-mediated medication management and in reducing potential adverse drug events in the outpatient clinic. METHODS/

DESIGN:

We are conducting a multicenter, cluster randomized controlled trial. The participants are specialists and residents working in the outpatient clinic of internal medicine, cardiology, pulmonology, geriatrics, gastroenterology and rheumatology. The intensive educational intervention is composed of a small-group session and e-learning. The primary outcome is discrepancies between registered medication (by physicians) and actually used medication (by patients). The key secondary outcomes are potential adverse events caused by missed drug-drug interactions. The primary and key secondary endpoints are being assessed shortly after the educational intervention is completed. Sample size will be calculated to ensure sufficient power. A sample size of 40 physicians per group and 20 patients per physician will ensure a power of >90 %, which means we will need a total of 80 physicians and 1,600 patients.

DISCUSSION:

We performed an exploratory trial wherein we tested the recruitment process, e-learning, time schedule, and methods for data collection, data management and data analysis. Accordingly, we refined the processes and content the recruitment strategy was intensified, extra measures were taken to facilitate smooth conductance of the e-learning and parts were made optional. First versions of the procedures for data collection were determined. Data entry and analysis was further standardized by using the G-standard database in the telephone questionnaire. TRIAL REGISTRATION ISRCTN registry ISRCTN50890124 . Registered 10 June 2013.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Educación Médica Continua / Administración del Tratamiento Farmacológico / Atención Ambulatoria / Instituciones de Atención Ambulatoria / Capacitación en Servicio / Errores de Medicación Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Qualitative_research Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Educación Médica Continua / Administración del Tratamiento Farmacológico / Atención Ambulatoria / Instituciones de Atención Ambulatoria / Capacitación en Servicio / Errores de Medicación Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Qualitative_research Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos
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