Decision Navigation for Advanced Prostate Cancer Treatment Options Using mHealth
2020年10月26日 更新者:Randy A. Jones、University of Virginia
Prostate cancer is a commonly diagnosed cancer, and is the second leading cause of cancer deaths among men in the U.S. The subgroup of men with advanced prostate cancer is particularly vulnerable to difficult choices for treatment because of the nature of their disease and having limited options.
This study will test the use of an innovative Registered Nurse-Community Patient Navigator team delivered interactive mHealth decision aid for patients with advanced prostate cancer to help facilitate informed shared decisions about anti-cancer treatment that affects their quality of life.
研究概览
详细说明
Many patients with advanced prostate cancer along with their decision partners/ proxies (DPP) struggle with complex treatment decisions, such as when to start, change, or stop cancer directed treatment.
Despite the utility of decision aids (DAs) to address decisional conflict, little is known about treatment decision-making for advanced cancers.
The study's primary aim is to test the effects of a theory- based mHealth DA (CHAMPION) administered by Registered Nurse (RN)-Community Patient Navigator (CPN) teams to advanced prostate cancer patients and decision partners/proxies on the following outcomes: less decisional conflict/uncertainty, higher psychosocial quality of life domain (HRQL-PSY), and less regret at the time of making an anti-cancer treatment decision.
The secondary aim is to evaluate the CPN role in delivery of the mHealth DA (CHAMPION) from the patients' and decision partners/proxies' perspective.
Preliminary estimates of treatment effects by race to see if the data support a larger effect among African Americans versus Others in the primary and secondary aims will also be explored.
This mixed-methods population-based randomized controlled trial will gather data from 158 patient/DPP pairs at three sites: University of Virginia Emily Couric Cancer Center, the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, and Virginia Commonwealth University Massey Cancer Center.
The pretest/posttest design will measure a time period that includes three single-event decisions over the course of their cancer-directed treatment; and a qualitative retrospective design will allow exploring the experiences of both patients and their DPPs separately in an interview at the completion of the study.
Stratification by race (African-American and Caucasian/Other) and decision point (starting vs. changing vs. stopping anticancer treatment) will be used.
There will be two groups: the control (enhanced usual care [EUC]) group and the decision intervention (DI) group.
The DI group will receive an interactive 7-component cognitive-behavioral skills mHealth program (DA) with a RN-CPN team, primarily focusing on decision-making during cancer treatment.
Self-report measures will be used for all participants in addition to probes for the taped interviews with DI.
The primary outcome measures are 1) decisional conflict (uncertainty), 2) decisional regret, 3) HRQL-PSY, and 4) decision-making participation preference.
Generalized linear models will be used for data analysis for the quantitative component, and qualitative evaluation of the intervention will be conducted to capture each pair's experience of the CHAMPION intervention.
This innovative mHealth DA delivered by a CPN is expected to increase acceptability and the uptake of both the DA and the technology components.
This addresses several NIH/NINR innovative questions, through the use of information technology to promote health-related decision-making for providers and patients, examining patient outcomes for improvement in healthcare, as well as to engage and support individuals such as extended family, lay coaches, etc. to augment provider care and recommendations.
研究类型
介入性
注册 (预期的)
316
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Maryland
-
Baltimore、Maryland、美国、21205
- 招聘中
- Johns Hopkins University
-
接触:
- Jennifer Wenzel, PhD,RN,FAAN
- 电话号码:410-502-1114
- 邮箱:jwenzel@jhu.edu
-
-
Virginia
-
Charlottesville、Virginia、美国、22908
- 招聘中
- University of Virginia
-
接触:
- Randy A Jones, PhD,RN,FAAN
- 电话号码:434-924-0125
- 邮箱:raj9c@virginia.edu
-
接触:
- Jane Gildersleeve, MSN
- 电话号码:434-243-3955
- 邮箱:jlg2g@virginia.edu
-
Richmond、Virginia、美国、23219
- 招聘中
- Virginia Commonwealth University
-
接触:
- Richard Brown, PhD
- 电话号码:804-628-3340
- 邮箱:rbrown39@vcu.edu
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- 1) stages III/ IV prostate cancer 2) life expectancy ≥6 months 3) Karnofsky Performance Status >60 4) willingness of a DPP (patient selected person who provides decisional support) to participate 5) pair ages >18 years 6) ability to understand English
Exclusion Criteria:
- severe psychiatric problems
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:支持治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
无干预:Enhanced Usual Care
Receive standard care
|
|
|
实验性的:Decision Intervention
Receives decision aid intervention that encompasses balance sheets, navigation, audio files, and interaction -- Cancer Health Aid to Manage Preferences and Improve Outcomes through Navigation (CHAMPION)
|
An interactive mHealth decision aid that includes immediate and over time quality of life (QL) graphical summaries for advanced prostate cancer patients to enhance informed, shared decision making and will also be used to assess the CPNs' role in the decision-making process.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Decision Conflict, Decision Regret, and Prostate Cancer Symptom Scale
大体时间:9 months
|
demonstrate less decisional conflict/uncertainty, higher QL (HRQL-PSY domain) and less regret at the time of making an anti-cancer treatment decision
|
9 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
semi-structured interview
大体时间:9 months
|
evaluate community patient navigator role in delivery of decision aid
|
9 months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Randy A Jones, PhD,RN,FAAN、University of Virginia
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2017年7月21日
初级完成 (预期的)
2021年12月31日
研究完成 (预期的)
2021年12月31日
研究注册日期
首次提交
2017年10月26日
首先提交符合 QC 标准的
2017年10月26日
首次发布 (实际的)
2017年10月31日
研究记录更新
最后更新发布 (实际的)
2020年10月28日
上次提交的符合 QC 标准的更新
2020年10月26日
最后验证
2020年10月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.