此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

弥合差距:利用Veris Health癌症护理平台为服务不足人群提升癌症护理

2026年9月18日 更新者:VERIS HEALTH INC

弥合差距:通过Veris Health癌症护理平台改善服务不足人群的癌症护理

The proposed study aims to optimize and validate the Veris Cancer Care Platform for the needs of medically underserved cancer patients receiving outpatient cancer therapy. The Veris Health platform is a remote patient monitoring and communication system designed to bridge the gap between clinical visits and provide oncology care teams with objective data during high-risk periods.

This study will specifically focus on optimizing the Veris Health platform for patients with language barriers, limited access to technology, and socioeconomic disparities. By incorporating user-centered design and working closely with community health centers, the research team will ensure that the platform is culturally and linguistically appropriate, easy to use, and accessible for all patients.

The study will use a mixed-methods approach to validate the effectiveness of the optimized platform, including quantitative data analysis and qualitative interviews with patients and healthcare providers. The goal is to demonstrate the potential for the Veris Health platform to improve outcomes for vulnerable populations by reducing hospitalizations, emergency department visits, and the economic burden of cancer care.

研究概览

研究类型

观察性的

注册 (估计的)

50

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。

学习联系方式

学习地点

    • Ohio
      • Columbus、Ohio、美国、43210
        • 招聘中
        • The Ohio State University
        • 接触:

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

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Underserved population undergoing Cancer treatment with at least one on the following barriers to healthcare access: Spanish as primary language, uninsured, insured with Medicaid, dual eligible for Medicare and Medicaid.

描述

Inclusion Criteria:

  • Adults > 18 years old
  • Diagnosis of cancer
  • ECOG Performance Status of 0-2
  • Undergoing or initiating systemic anticancer therapy
  • Able to utilize and interact with a mobile application and in-home devices for physiological monitoring. Have at least one of the following barriers to healthcare access: Spanish as primary language, uninsured, insured with Medicaid, dual eligible for Medicare and Medicaid

Exclusion Criteria:

-N/A

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

  • 观测模型:COHORT
  • 时间观点:PROSPECTIVE

队列和干预

团体/队列
干预/治疗
Main Phase group

All participating subject utilizing the Veris Health app will complete all study health measurements with a 24 week period on the Veris Health app as well as participate in interviews and focus groups.

Veris Health offers at-home devices to monitor multiple physiological parameters, including temperature, heart rate, oxygen saturation, blood pressure, weight, and activity (step count). Patients are provided with a home cellular hub that is already paired to peripheral devices via Bluetooth. The hub communicates with all devices and the local cellular network out-of-the-box, and data is automatically sent via cellular network to the Veris Health backend database, making it easy for patients to use the system. Patients are responsible for taking their vital sign measurements daily. The devices automatically send the measurement data to the Veris Health HIPAA compliant, secure cloud server via the preconnected cellular hub.

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
Usability of the Veris Health Cancer Care Platform
大体时间:5 Months

Usability of the Veris Health Cancer Care platform as assessed by the Software Usability Measurement Inventory (SUMI) among patients, caretakers, and healthcare teams.

Measure: SUMI total and domain scores

Time Frame: During study participation

5 Months
Product Design Usability and Acceptability
大体时间:5 Months

Ease of use, accessibility, and acceptability of the Veris Health Cancer Care platform based on A/B testing of product design features.

Measure: Comparative usability metrics (e.g., task completion success, user preference)

Time Frame: During study participation

5 Months
User Needs and Preferences
大体时间:5 Months

User-identified needs, preferences, and barriers to use of the Veris Health Cancer Care platform.

Measure: Qualitative themes derived from user interviews and focus groups

Time Frame: During study participation

5 Months

次要结果测量

结果测量
措施说明
大体时间
Health-Related Quality of Life (HRQL)
大体时间:5 Months

Change in health-related quality of life among participants using the Veris Health Cancer Care platform.

Measure: EQ-5D Index score

5 Months
Symptom Burden of Cancer Treatment Side Effects
大体时间:5 Months

Frequency and severity of cancer treatment-related symptoms, including nausea, diarrhea, and infection.

Measure: Patient-reported symptom frequency and severity scores

5 Months
Cancer Treatment Adherence and Duration
大体时间:5 months

Adherence to prescribed cancer therapy and treatment duration.

Measure: Rates of dose reductions, early treatment discontinuation, and treatment duration

5 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。

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。

有用的网址

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)

2026年3月11日

初级完成 (估计的)

2027年11月30日

研究完成 (估计的)

2027年11月30日

研究注册日期

首次提交

2026年1月27日

首先提交符合 QC 标准的

2026年2月3日

首次发布 (实际的)

2026年2月9日

研究记录更新

最后更新发布 (实际的)

2026年9月23日

上次提交的符合 QC 标准的更新

2026年9月18日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • VER-PR-0023
  • 5R44MD019611-02 (美国 NIH 拨款/合同)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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.

订阅