Cargando…

Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol

BACKGROUND: The prescribing of high-risk medications to older adults remains extremely common and results in potentially avoidable health consequences. Efforts to reduce prescribing have had limited success, in part because they have been sub-optimally timed, poorly designed, or not provided actiona...

Descripción completa

Detalles Bibliográficos
Autores principales: Lauffenburger, Julie C., Isaac, Thomas, Trippa, Lorenzo, Keller, Punam, Robertson, Ted, Glynn, Robert J., Sequist, Thomas D., Kim, Dae H., Fontanet, Constance P., Castonguay, Edward W. B., Haff, Nancy, Barlev, Renee A., Mahesri, Mufaddal, Gopalakrishnan, Chandrashekar, Choudhry, Niteesh K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792313/
https://www.ncbi.nlm.nih.gov/pubmed/33413494
http://dx.doi.org/10.1186/s13012-020-01078-9
_version_ 1783633778381422592
author Lauffenburger, Julie C.
Isaac, Thomas
Trippa, Lorenzo
Keller, Punam
Robertson, Ted
Glynn, Robert J.
Sequist, Thomas D.
Kim, Dae H.
Fontanet, Constance P.
Castonguay, Edward W. B.
Haff, Nancy
Barlev, Renee A.
Mahesri, Mufaddal
Gopalakrishnan, Chandrashekar
Choudhry, Niteesh K.
author_facet Lauffenburger, Julie C.
Isaac, Thomas
Trippa, Lorenzo
Keller, Punam
Robertson, Ted
Glynn, Robert J.
Sequist, Thomas D.
Kim, Dae H.
Fontanet, Constance P.
Castonguay, Edward W. B.
Haff, Nancy
Barlev, Renee A.
Mahesri, Mufaddal
Gopalakrishnan, Chandrashekar
Choudhry, Niteesh K.
author_sort Lauffenburger, Julie C.
collection PubMed
description BACKGROUND: The prescribing of high-risk medications to older adults remains extremely common and results in potentially avoidable health consequences. Efforts to reduce prescribing have had limited success, in part because they have been sub-optimally timed, poorly designed, or not provided actionable information. Electronic health record (EHR)-based tools are commonly used but have had limited application in facilitating deprescribing in older adults. The objective is to determine whether designing EHR tools using behavioral science principles reduces inappropriate prescribing and clinical outcomes in older adults. METHODS: The Novel Uses of Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) project uses a two-stage, 16-arm adaptive randomized pragmatic trial with a “pick-the-winner” design to identify the most effective of many potential EHR tools among primary care providers and their patients ≥ 65 years chronically using benzodiazepines, sedative hypnotic (“Z-drugs”), or anticholinergics in a large integrated delivery system. In stage 1, we randomized providers and their patients to usual care (n = 81 providers) or one of 15 EHR tools (n = 8 providers per arm) designed using behavioral principles including salience, choice architecture, or defaulting. After 6 months of follow-up, we will rank order the arms based upon their impact on the trial’s primary outcome (for both stages): reduction in inappropriate prescribing (via discontinuation or tapering). In stage 2, we will randomize (a) stage 1 usual care providers in a 1:1 ratio to one of the up to 5 most promising stage 1 interventions or continue usual care and (b) stage 1 providers in the unselected arms in a 1:1 ratio to one of the 5 most promising interventions or usual care. Secondary and tertiary outcomes include quantities of medication prescribed and utilized and clinically significant adverse outcomes. DISCUSSION: Stage 1 launched in October 2020. We plan to complete stage 2 follow-up in December 2021. These results will advance understanding about how behavioral science can optimize EHR decision support to improve prescribing and health outcomes. Adaptive trials have rarely been used in implementation science, so these findings also provide insight into how trials in this field could be more efficiently conducted. TRIAL REGISTRATION: Clinicaltrials.gov (NCT04284553, registered: February 26, 2020) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13012-020-01078-9.
format Online
Article
Text
id pubmed-7792313
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-77923132021-01-11 Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol Lauffenburger, Julie C. Isaac, Thomas Trippa, Lorenzo Keller, Punam Robertson, Ted Glynn, Robert J. Sequist, Thomas D. Kim, Dae H. Fontanet, Constance P. Castonguay, Edward W. B. Haff, Nancy Barlev, Renee A. Mahesri, Mufaddal Gopalakrishnan, Chandrashekar Choudhry, Niteesh K. Implement Sci Study Protocol BACKGROUND: The prescribing of high-risk medications to older adults remains extremely common and results in potentially avoidable health consequences. Efforts to reduce prescribing have had limited success, in part because they have been sub-optimally timed, poorly designed, or not provided actionable information. Electronic health record (EHR)-based tools are commonly used but have had limited application in facilitating deprescribing in older adults. The objective is to determine whether designing EHR tools using behavioral science principles reduces inappropriate prescribing and clinical outcomes in older adults. METHODS: The Novel Uses of Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) project uses a two-stage, 16-arm adaptive randomized pragmatic trial with a “pick-the-winner” design to identify the most effective of many potential EHR tools among primary care providers and their patients ≥ 65 years chronically using benzodiazepines, sedative hypnotic (“Z-drugs”), or anticholinergics in a large integrated delivery system. In stage 1, we randomized providers and their patients to usual care (n = 81 providers) or one of 15 EHR tools (n = 8 providers per arm) designed using behavioral principles including salience, choice architecture, or defaulting. After 6 months of follow-up, we will rank order the arms based upon their impact on the trial’s primary outcome (for both stages): reduction in inappropriate prescribing (via discontinuation or tapering). In stage 2, we will randomize (a) stage 1 usual care providers in a 1:1 ratio to one of the up to 5 most promising stage 1 interventions or continue usual care and (b) stage 1 providers in the unselected arms in a 1:1 ratio to one of the 5 most promising interventions or usual care. Secondary and tertiary outcomes include quantities of medication prescribed and utilized and clinically significant adverse outcomes. DISCUSSION: Stage 1 launched in October 2020. We plan to complete stage 2 follow-up in December 2021. These results will advance understanding about how behavioral science can optimize EHR decision support to improve prescribing and health outcomes. Adaptive trials have rarely been used in implementation science, so these findings also provide insight into how trials in this field could be more efficiently conducted. TRIAL REGISTRATION: Clinicaltrials.gov (NCT04284553, registered: February 26, 2020) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13012-020-01078-9. BioMed Central 2021-01-07 /pmc/articles/PMC7792313/ /pubmed/33413494 http://dx.doi.org/10.1186/s13012-020-01078-9 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Lauffenburger, Julie C.
Isaac, Thomas
Trippa, Lorenzo
Keller, Punam
Robertson, Ted
Glynn, Robert J.
Sequist, Thomas D.
Kim, Dae H.
Fontanet, Constance P.
Castonguay, Edward W. B.
Haff, Nancy
Barlev, Renee A.
Mahesri, Mufaddal
Gopalakrishnan, Chandrashekar
Choudhry, Niteesh K.
Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title_full Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title_fullStr Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title_full_unstemmed Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title_short Rationale and design of the Novel Uses of adaptive Designs to Guide provider Engagement in Electronic Health Records (NUDGE-EHR) pragmatic adaptive randomized trial: a trial protocol
title_sort rationale and design of the novel uses of adaptive designs to guide provider engagement in electronic health records (nudge-ehr) pragmatic adaptive randomized trial: a trial protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792313/
https://www.ncbi.nlm.nih.gov/pubmed/33413494
http://dx.doi.org/10.1186/s13012-020-01078-9
work_keys_str_mv AT lauffenburgerjuliec rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT isaacthomas rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT trippalorenzo rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT kellerpunam rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT robertsonted rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT glynnrobertj rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT sequistthomasd rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT kimdaeh rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT fontanetconstancep rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT castonguayedwardwb rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT haffnancy rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT barlevreneea rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT mahesrimufaddal rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT gopalakrishnanchandrashekar rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol
AT choudhryniteeshk rationaleanddesignofthenovelusesofadaptivedesignstoguideproviderengagementinelectronichealthrecordsnudgeehrpragmaticadaptiverandomizedtrialatrialprotocol