跳至主要内容
临床试验/NCT05562778
NCT05562778招募中不适用

Evaluation of a Chatbot to Maximize Hereditary Cancer Genetic Risk Assessment in an Underserved Gynecology Population

Weill Medical College of Cornell University8 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2023年1月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
150
试验地点
8
主要终点
Proportion recommended genetic testing

研究概览

简要总结

In this study, the investigators aim to compare a mobile health platform, known as a 'chatbot,' that leverages artificial intelligence and natural language processing to scale communication, to 'usual care' that patients would receive. This comparison will enable the investigators to determine if the chatbot system can improve rates of recommendation for genetic testing among patients at elevated risk of harboring a familial cancer syndrome in an all-Medicaid gynecology clinic. Furthermore, the investigators aim to evaluate facilitators of inequity in regard to patient access to and utilization of genetic testing services.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • 8 years of age or older.
  • Scheduled for a New Patient appointment in the gynecology clinic. Speaks and reads in English.
  • Access to a telephone with texting capacity.
  • Has not had prior genetic testing for hereditary cancer syndromes.

排除标准

  • Under 18 years of age
  • Has had previous genetic testing for hereditary cancer syndromes
  • Does not read/speak in English
  • Does not have access to a phone with texting capabilities

研究组 & 干预措施

Chatbot

Experimental

Subjects will receive a text message initiating a chatbot conversation that relies on natural language processing to gather personal and family cancer. Subjects are identified by the chatbot as meeting National Comprehensive Cancer Network (NCCN) high-risk criteria. Next, subjects undergo pre-test genetic counseling via the chatbot and then clinicians are notified (via the chatbot portal) that the subject meets high-risk criteria. For subjects meeting high-risk criteria (based on the chatbot evaluation), the clinician will complete genetic counseling and recommend genetic testing during the visit. For subjects interested in genetic testing, the clinician will order genetic testing.

干预措施: Chatbot (Other)

Usual Care

No Intervention

Personal and family cancer history will be collected by the clinician during the subject's visit. Clinicians will evaluate the patient's personal/family history according to National Comprehensive Cancer Network (NCCN) high-risk criteria. For subjects recognized by the clinician as meeting NCCN criteria, the clinician will complete genetic counseling and recommend genetic testing. For subjects interested in genetic testing, the clinician will order genetic testing.

结局指标

主要结局

Proportion recommended genetic testing

时间窗: 2 years

The proportion of high-risk patients that are recommended genetic testing for familial cancer syndromes in the chatbot vs. usual care arms.

次要结局

  • Proportion completed recommended genetic testing(2 years)
  • Barriers to genetic testing(2 years)
  • Facilitator of inequity in the utilization of genetic services(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

Loading locations...

相似试验