Understanding the Role of MyCareGorithm as a Visual Digital Platforms in Cancer Treatment Education and Patient Comprehension of Oncology Treatment Plans
The purpose of this research study is to learn if a digital communication tool can improve how well patients with head and neck cancer and their caregivers understand the disease and treatment plan after their first consultation visit with the doctor/nurse practitioner.
研究概览
详细说明
Primary Objective:
The primary objective of this pilot study is to determine whether use of a novel digital visual communication tool improves patient understanding and satisfaction with their initial multidisciplinary consultation for head and neck and prostate cancer. Specifically, the study seeks to answer the scientific question:
• Do at least 75% of newly diagnosed head and neck and prostate cancer patients report being "satisfied" (≥4 positive responses on a 6-item survey) after use of the digital communication tool, and is this proportion significantly greater than 50%?
Secondary Objectives:
Caregiver Understanding and Satisfaction
• What proportion of caregivers of newly diagnosed patients report satisfaction with their understanding of the patient's disease and treatment after using the tool, and how confident can we be in this estimate (95% Clopper-Pearson CI)?
Provider Experience and Communication Effectiveness
• What proportion of providers report satisfaction (≥5 positive responses on a 7-item survey) with the tool's ability to improve communication efficiency and consultation quality for patients they treated?
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名：Steven J Frank, MD
- 电话号码：(713) 563-3601
- 邮箱：sjfrank@mdanderson.org
学习地点
-
-
Texas
-
Houston、Texas、美国、77030
- UT MD Anderson
-
接触：
- Steven J Frank, MD
- 电话号码：713-563-3601
- 邮箱：sjfrank@mdanderson.org
-
首席研究员：
- Steven Frank, MD
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
Patients
- Adults aged 18 to 100 years.
- Diagnosed with head and neck cancer (all histologies included).
- Receiving treatment for head and neck and prostate cancer at MDACC
- Able to speak and understand English
Caregivers
- Adults (≥18 years old).
- Identified as a caregiver to a patient who meets the above patient inclusion criteria.
- Able to speak and understand English.
Providers
- Doctors or nurse practitioners practicing in the field of radiation oncology and actively participating in initial consultations for patients with head and neck cancer and prostate cancer.
- Must complete the provider survey after the consultation.
Exclusion Criteria:
Patients
- Individuals without a diagnosis of head and neck cancer or prostate cancer.
- Patients who do not speak English (since the digital tool is not translated).
Caregivers
- Adults who are not caregivers of the eligible patient
- Caregivers who do not speak English (tool not translated).
Providers
- Doctors or nurse practitioners not practicing in the field of radiation oncology and not part of the initial consultation process.
学习计划
研究是如何设计的？
设计细节
- 主要用途：设备可行性
- 分配：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Patient/Caregiver: Use of MyCareGorithm
Following use of the digital visual communication tool by the provider, patients and any accompanying caregivers will be asked to complete their surveys via REDCap. Providers will complete their survey immediately after the consultation with each participating patient, also via REDCap. Each survey requires approximately 5 minutes to complete. No follow-up surveys or repeat administrations are planned. |
A 6-item structured questionnaire with Yes/No response options, followed by one open-ended free-text question. |
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 |
|---|---|---|
|
Safety and Adverse Events (AEs)
大体时间：Through study completion; an average of 1 year
|
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0 |
Through study completion; an average of 1 year
|
合作者和调查者
调查人员
- 首席研究员：Steven J Frank, MD、UT MD Anderson
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
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.