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临床试验/NCT05535140
NCT05535140已完成不适用

Chatbot Powered G8 Screening Intervention

Thomas Jefferson University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
Number of Participants Who Agree to Using the G8 Assessment

研究概览

简要总结

In this prospective quality improvement study, we will develop and evaluate the feasibility and acceptability of an online patient self-reported G8 screening tool which will allow us to efficiently identify G8 positive older cancer patients to be referred to our Senior Adult Oncology Center (SAOC) for a Comprehensive Geriatric Assessment (CGA).

详细描述

We will test the feasibility and acceptability of the online G8 screening tool developed. 100 older new established cancer patients who had used the MyChart G8 will be recruited to provide their feedback on the usability of the screening tool and any related referral and SAOC appointment experience. Among patients with G8 scores ≤ 14, they will be referred to a CGA. We will examine CGA attendance compliance, predictive value of the online collected G8 score with the final frailty designation determined by the CGA, and perceived barriers among CGA non-adherent patients via a brief follow up inquiry.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •65 years and older
  • •New Patient Visit scheduled for Medical Oncology

排除标准

  • •Inability to answer or have caregiver answer questions on screening tool.

研究组 & 干预措施

Cancer patients who are 65 years of age or older

An online self-reported G8 screening tool. The tool will have content including: 1) the purpose and benefit of the G8, 2) explanations of each question with examples and probes to help with recall, and 3) next steps after the G8 assessment is completed and how the results might impact their cancer treatments. New established older cancer patients will be invited to interact with the tool.

干预措施: G8 Screening Tool (Other)

结局指标

主要结局

Number of Participants Who Agree to Using the G8 Assessment

时间窗: At Baseline

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

Number of Participants Who Complete the G8 Assessment

时间窗: At Baseline (approximately 15 minutes)

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

Number of Participants Who Complete the Referred SAOC Visits if They Complete the G8 Assessment and Are Screened Positive

时间窗: Approximately 2 weeks after G8 completion

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

Agree to using the G8 assessment

时间窗: At time of visit

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

3. Complete the referred SAOC visits if they complete the G8 assessment and are screened positive

时间窗: After visit

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

Complete the G8 assessment

时间窗: At time of visit

To determine the feasibility of implementing an online patient self-reported G8 assessment, on new patients \>65y/o who are scheduled with the medical oncology department.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kuang-Yi Wen

Professor - Medical Oncology

Thomas Jefferson University

研究点 (2)

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