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Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial

BACKGROUND: Although prostate cancer is the most common cancer among veterans receiving care in the Veterans Health Administration (VA), more needs to be done to understand and improve survivorship care for this large population. This study, funded by VA Health Services Research & Development (H...

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Autores principales: Skolarus, Ted A., Metreger, Tabitha, Hwang, Soohyun, Kim, Hyungjin Myra, Grubb, Robert L., Gingrich, Jeffrey R., Hawley, Sarah T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395886/
https://www.ncbi.nlm.nih.gov/pubmed/28420419
http://dx.doi.org/10.1186/s13063-017-1925-4
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author Skolarus, Ted A.
Metreger, Tabitha
Hwang, Soohyun
Kim, Hyungjin Myra
Grubb, Robert L.
Gingrich, Jeffrey R.
Hawley, Sarah T.
author_facet Skolarus, Ted A.
Metreger, Tabitha
Hwang, Soohyun
Kim, Hyungjin Myra
Grubb, Robert L.
Gingrich, Jeffrey R.
Hawley, Sarah T.
author_sort Skolarus, Ted A.
collection PubMed
description BACKGROUND: Although prostate cancer is the most common cancer among veterans receiving care in the Veterans Health Administration (VA), more needs to be done to understand and improve survivorship care for this large population. This study, funded by VA Health Services Research & Development (HSR&D), seeks to address the need to improve patient-centered survivorship care for veterans with prostate cancer. METHODS/DESIGN: This is a two-armed randomized controlled trial (RCT) with a target enrollment of up to 325 prostate cancer survivors per study arm (total anticipated n = 600). Patients will be recruited from four VA sites. Patient eligibility criteria include age range of 40–80 years, one to ten years post-treatment, and currently experiencing prostate cancer symptom burden. We will compare the “Building Your New Normal” program, a personally-tailored automated telephone symptom management intervention for improving symptom self-management to usual care enhanced with a non-tailored newsletter about symptom management. Primary outcomes include changes in symptom burden, bother, and health services utilization at five and 12 months after enrollment. Secondary outcomes include long-term psychosocial outcomes (e.g. subjective health, perceived cancer control). We will use multivariable regression analysis to evaluate the impact of the intervention on primary and secondary outcomes. We will conduct a process evaluation to understand the effective intervention components and explore possibilities for broader implementation and dissemination. DISCUSSION: Our central hypothesis is that intervention group participants will have improved and more confident symptom self-management and prostate cancer quality of life following the intervention and that these outcomes will translate to more efficient use of health services. The study results will provide much needed information about how to optimize the quality of care, and life, of veteran prostate cancer survivors. TRIAL REGISTRATION: ClinicalTrials.gov ID NCT01900561; Registered on 22 July 2013. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-1925-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-53958862017-04-20 Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial Skolarus, Ted A. Metreger, Tabitha Hwang, Soohyun Kim, Hyungjin Myra Grubb, Robert L. Gingrich, Jeffrey R. Hawley, Sarah T. Trials Study Protocol BACKGROUND: Although prostate cancer is the most common cancer among veterans receiving care in the Veterans Health Administration (VA), more needs to be done to understand and improve survivorship care for this large population. This study, funded by VA Health Services Research & Development (HSR&D), seeks to address the need to improve patient-centered survivorship care for veterans with prostate cancer. METHODS/DESIGN: This is a two-armed randomized controlled trial (RCT) with a target enrollment of up to 325 prostate cancer survivors per study arm (total anticipated n = 600). Patients will be recruited from four VA sites. Patient eligibility criteria include age range of 40–80 years, one to ten years post-treatment, and currently experiencing prostate cancer symptom burden. We will compare the “Building Your New Normal” program, a personally-tailored automated telephone symptom management intervention for improving symptom self-management to usual care enhanced with a non-tailored newsletter about symptom management. Primary outcomes include changes in symptom burden, bother, and health services utilization at five and 12 months after enrollment. Secondary outcomes include long-term psychosocial outcomes (e.g. subjective health, perceived cancer control). We will use multivariable regression analysis to evaluate the impact of the intervention on primary and secondary outcomes. We will conduct a process evaluation to understand the effective intervention components and explore possibilities for broader implementation and dissemination. DISCUSSION: Our central hypothesis is that intervention group participants will have improved and more confident symptom self-management and prostate cancer quality of life following the intervention and that these outcomes will translate to more efficient use of health services. The study results will provide much needed information about how to optimize the quality of care, and life, of veteran prostate cancer survivors. TRIAL REGISTRATION: ClinicalTrials.gov ID NCT01900561; Registered on 22 July 2013. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-1925-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-18 /pmc/articles/PMC5395886/ /pubmed/28420419 http://dx.doi.org/10.1186/s13063-017-1925-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Study Protocol
Skolarus, Ted A.
Metreger, Tabitha
Hwang, Soohyun
Kim, Hyungjin Myra
Grubb, Robert L.
Gingrich, Jeffrey R.
Hawley, Sarah T.
Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title_full Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title_fullStr Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title_full_unstemmed Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title_short Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
title_sort optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395886/
https://www.ncbi.nlm.nih.gov/pubmed/28420419
http://dx.doi.org/10.1186/s13063-017-1925-4
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