Cargando…

Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice

BACKGROUND: Online information retrieval systems have the potential to improve patient care but there are few comparative studies of the impact of online evidence on clinicians' decision-making behaviour in routine clinical work. METHODS/DESIGN: A randomized controlled parallel design is employ...

Descripción completa

Detalles Bibliográficos
Autores principales: Coiera, Enrico, Magrabi, Farah, Westbrook, Johanna I, Kidd, Michael R, Day, Richard O
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564384/
https://www.ncbi.nlm.nih.gov/pubmed/16928282
http://dx.doi.org/10.1186/1472-6947-6-33
_version_ 1782129560465178624
author Coiera, Enrico
Magrabi, Farah
Westbrook, Johanna I
Kidd, Michael R
Day, Richard O
author_facet Coiera, Enrico
Magrabi, Farah
Westbrook, Johanna I
Kidd, Michael R
Day, Richard O
author_sort Coiera, Enrico
collection PubMed
description BACKGROUND: Online information retrieval systems have the potential to improve patient care but there are few comparative studies of the impact of online evidence on clinicians' decision-making behaviour in routine clinical work. METHODS/DESIGN: A randomized controlled parallel design is employed to assess the effectiveness of an online evidence retrieval system, Quick Clinical (QC) in improving clinical decision-making processes in general practice. Eligible clinicians are randomised either to receive access or not to receive access to QC in their consulting rooms for 12 months. Participants complete pre- and post trial surveys. Two-hundred general practitioners are recruited. Participants must be registered to practice in Australia, have a computer with Internet access in their consulting room and use electronic prescribing. Clinicians planning to retire or move to another practice within 12 months or participating in any other clinical trial involving electronic extraction of prescriptions data are excluded from the study. The primary end-points for the study is clinician acceptance and use of QC and the resulting change in decision-making behaviour. The study will examine prescribing patterns related to frequently prescribed medications where there has been a recent significant shift in recommendations regarding their use based upon new evidence. Secondary outcome measures include self-reported changes in diagnosis, patient education, prescriptions written, investigations and referrals. DISCUSSION: A trial under experimental conditions is an effective way of examining the impact of using QC in routine general practice consultations.
format Text
id pubmed-1564384
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15643842006-09-14 Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice Coiera, Enrico Magrabi, Farah Westbrook, Johanna I Kidd, Michael R Day, Richard O BMC Med Inform Decis Mak Study Protocol BACKGROUND: Online information retrieval systems have the potential to improve patient care but there are few comparative studies of the impact of online evidence on clinicians' decision-making behaviour in routine clinical work. METHODS/DESIGN: A randomized controlled parallel design is employed to assess the effectiveness of an online evidence retrieval system, Quick Clinical (QC) in improving clinical decision-making processes in general practice. Eligible clinicians are randomised either to receive access or not to receive access to QC in their consulting rooms for 12 months. Participants complete pre- and post trial surveys. Two-hundred general practitioners are recruited. Participants must be registered to practice in Australia, have a computer with Internet access in their consulting room and use electronic prescribing. Clinicians planning to retire or move to another practice within 12 months or participating in any other clinical trial involving electronic extraction of prescriptions data are excluded from the study. The primary end-points for the study is clinician acceptance and use of QC and the resulting change in decision-making behaviour. The study will examine prescribing patterns related to frequently prescribed medications where there has been a recent significant shift in recommendations regarding their use based upon new evidence. Secondary outcome measures include self-reported changes in diagnosis, patient education, prescriptions written, investigations and referrals. DISCUSSION: A trial under experimental conditions is an effective way of examining the impact of using QC in routine general practice consultations. BioMed Central 2006-08-24 /pmc/articles/PMC1564384/ /pubmed/16928282 http://dx.doi.org/10.1186/1472-6947-6-33 Text en Copyright © 2006 Coiera et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Coiera, Enrico
Magrabi, Farah
Westbrook, Johanna I
Kidd, Michael R
Day, Richard O
Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title_full Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title_fullStr Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title_full_unstemmed Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title_short Protocol for the Quick Clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
title_sort protocol for the quick clinical study: a randomised controlled trial to assess the impact of an online evidence retrieval system on decision-making in general practice
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564384/
https://www.ncbi.nlm.nih.gov/pubmed/16928282
http://dx.doi.org/10.1186/1472-6947-6-33
work_keys_str_mv AT coieraenrico protocolforthequickclinicalstudyarandomisedcontrolledtrialtoassesstheimpactofanonlineevidenceretrievalsystemondecisionmakingingeneralpractice
AT magrabifarah protocolforthequickclinicalstudyarandomisedcontrolledtrialtoassesstheimpactofanonlineevidenceretrievalsystemondecisionmakingingeneralpractice
AT westbrookjohannai protocolforthequickclinicalstudyarandomisedcontrolledtrialtoassesstheimpactofanonlineevidenceretrievalsystemondecisionmakingingeneralpractice
AT kiddmichaelr protocolforthequickclinicalstudyarandomisedcontrolledtrialtoassesstheimpactofanonlineevidenceretrievalsystemondecisionmakingingeneralpractice
AT dayrichardo protocolforthequickclinicalstudyarandomisedcontrolledtrialtoassesstheimpactofanonlineevidenceretrievalsystemondecisionmakingingeneralpractice