Skolarus Ted A, Metreger Tabitha, Hwang Soohyun, Kim Hyungjin Myra, Grubb Robert L, Gingrich Jeffrey R, Hawley Sarah T
VA HSR&D Center for Clinical Management Research, VA Ann Arbor Healthcare System, 2215 Fuller Road, Ann Arbor, MI, 48105, USA.
Department of Urology, Dow Division of Health Services Research, University of Michigan, Ann Arbor, MI, USA.
Trials. 2017 Apr 18;18(1):181. doi: 10.1186/s13063-017-1925-4.
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.
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.
ClinicalTrials.gov ID NCT01900561 ; Registered on 22 July 2013.
尽管前列腺癌是在退伍军人健康管理局(VA)接受治疗的退伍军人中最常见的癌症,但对于了解和改善这一庞大群体的生存护理仍有更多工作要做。这项由VA卫生服务研究与发展部(HSR&D)资助的研究旨在满足改善前列腺癌退伍军人以患者为中心的生存护理的需求。
方法/设计:这是一项双臂随机对照试验(RCT),每个研究组的目标入组人数高达325名前列腺癌幸存者(预计总数n = 600)。患者将从四个VA地点招募。患者入选标准包括年龄在40 - 80岁之间、治疗后一至十年、目前有前列腺癌症状负担。我们将比较“建立你的新常态”计划,这是一种针对改善症状自我管理的个性化自动电话症状管理干预措施,与通过一份关于症状管理的非个性化时事通讯加强的常规护理。主要结局包括入组后5个月和12个月时症状负担、困扰及卫生服务利用情况的变化。次要结局包括长期心理社会结局(如主观健康、感知癌症控制)。我们将使用多变量回归分析来评估干预对主要和次要结局的影响。我们将进行过程评估以了解有效干预成分,并探索更广泛实施和传播的可能性。
我们的核心假设是,干预组参与者在干预后将改善并更自信地进行症状自我管理以及提高前列腺癌生活质量,并且这些结局将转化为更有效地利用卫生服务。研究结果将提供关于如何优化退伍军人前列腺癌幸存者护理质量和生活质量的急需信息。
ClinicalTrials.gov标识符NCT01900561;于2013年7月22日注册。