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Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study
BACKGROUND: Many patients with diabetes have poor blood pressure (BP) control. Pharmacological therapy is the cornerstone of effective BP treatment, yet there are high rates both of poor medication adherence and failure to intensify medications. Successful medication management requires an effective...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967508/ https://www.ncbi.nlm.nih.gov/pubmed/20939913 http://dx.doi.org/10.1186/1745-6215-11-95 |
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author | Heisler, Michele Hofer, Timothy P Klamerus, Mandi L Schmittdiel, Julie Selby, Joe Hogan, Mary M Bosworth, Hayden B Tremblay, Adam Kerr, Eve A |
author_facet | Heisler, Michele Hofer, Timothy P Klamerus, Mandi L Schmittdiel, Julie Selby, Joe Hogan, Mary M Bosworth, Hayden B Tremblay, Adam Kerr, Eve A |
author_sort | Heisler, Michele |
collection | PubMed |
description | BACKGROUND: Many patients with diabetes have poor blood pressure (BP) control. Pharmacological therapy is the cornerstone of effective BP treatment, yet there are high rates both of poor medication adherence and failure to intensify medications. Successful medication management requires an effective partnership between providers who initiate and increase doses of effective medications and patients who adhere to the regimen. METHODS: In this cluster-randomized controlled effectiveness study, primary care teams within sites were randomized to a program led by a clinical pharmacist trained in motivational interviewing-based behavioral counseling approaches and authorized to make BP medication changes or to usual care. This study involved the collection of data during a 14-month intervention period in three Department of Veterans Affairs facilities and two Kaiser Permanente Northern California facilities. The clinical pharmacist was supported by clinical information systems that enabled proactive identification of, and outreach to, eligible patients identified on the basis of poor BP control and either medication refill gaps or lack of recent medication intensification. The primary outcome is the relative change in systolic blood pressure (SBP) measurements over time. Secondary outcomes are changes in Hemoglobin A1c, low-density lipoprotein cholesterol (LDL), medication adherence determined from pharmacy refill data, and medication intensification rates. DISCUSSION: Integration of the three intervention elements - proactive identification, adherence counseling and medication intensification - is essential to achieve optimal levels of control for high-risk patients. Testing the effectiveness of this intervention at the team level allows us to study the program as it would typically be implemented within a clinic setting, including how it integrates with other elements of care. TRIAL REGISTRATION: The ClinicalTrials.gov registration number is NCT00495794. |
format | Text |
id | pubmed-2967508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29675082010-11-02 Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study Heisler, Michele Hofer, Timothy P Klamerus, Mandi L Schmittdiel, Julie Selby, Joe Hogan, Mary M Bosworth, Hayden B Tremblay, Adam Kerr, Eve A Trials Study Protocol BACKGROUND: Many patients with diabetes have poor blood pressure (BP) control. Pharmacological therapy is the cornerstone of effective BP treatment, yet there are high rates both of poor medication adherence and failure to intensify medications. Successful medication management requires an effective partnership between providers who initiate and increase doses of effective medications and patients who adhere to the regimen. METHODS: In this cluster-randomized controlled effectiveness study, primary care teams within sites were randomized to a program led by a clinical pharmacist trained in motivational interviewing-based behavioral counseling approaches and authorized to make BP medication changes or to usual care. This study involved the collection of data during a 14-month intervention period in three Department of Veterans Affairs facilities and two Kaiser Permanente Northern California facilities. The clinical pharmacist was supported by clinical information systems that enabled proactive identification of, and outreach to, eligible patients identified on the basis of poor BP control and either medication refill gaps or lack of recent medication intensification. The primary outcome is the relative change in systolic blood pressure (SBP) measurements over time. Secondary outcomes are changes in Hemoglobin A1c, low-density lipoprotein cholesterol (LDL), medication adherence determined from pharmacy refill data, and medication intensification rates. DISCUSSION: Integration of the three intervention elements - proactive identification, adherence counseling and medication intensification - is essential to achieve optimal levels of control for high-risk patients. Testing the effectiveness of this intervention at the team level allows us to study the program as it would typically be implemented within a clinic setting, including how it integrates with other elements of care. TRIAL REGISTRATION: The ClinicalTrials.gov registration number is NCT00495794. BioMed Central 2010-10-12 /pmc/articles/PMC2967508/ /pubmed/20939913 http://dx.doi.org/10.1186/1745-6215-11-95 Text en Copyright ©2010 Heisler 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 Heisler, Michele Hofer, Timothy P Klamerus, Mandi L Schmittdiel, Julie Selby, Joe Hogan, Mary M Bosworth, Hayden B Tremblay, Adam Kerr, Eve A Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title | Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title_full | Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title_fullStr | Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title_full_unstemmed | Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title_short | Study protocol: The Adherence and Intensification of Medications (AIM) study - a cluster randomized controlled effectiveness study |
title_sort | study protocol: the adherence and intensification of medications (aim) study - a cluster randomized controlled effectiveness study |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967508/ https://www.ncbi.nlm.nih.gov/pubmed/20939913 http://dx.doi.org/10.1186/1745-6215-11-95 |
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