NCT06537687已完成不适用
Relational Agents in Cervical Cancer Education (RACE)
Radhika Gogoi2 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2020年11月18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
- 发起方
- 入组人数
- 91
- 试验地点
- 2
- 主要终点
- Participation Rate
研究概览
简要总结
The goal of this clinical trial is to assess the feasibility of using interactive teaching to educate cervical cancer patients about Human papillomavirus (HPV) and HPV vaccinations.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Adults aged 18 and older
- •Patients with an ICD9 diagnosis of cervical/vaginal/vulvar cancer or dysplasia receiving care at Karmanos Cancer Institute or OU Health Stephenson Cancer Center
排除标准
- •Patients who are recorded in the EHR as requesting to be removed from research
- •Non-English speakers
- •Any cognitive disability that prevents informed consent
- •Any individual recruited in previous phases of the Study will be excluded.
研究组 & 干预措施
Control
Active Comparator
The control group will be given a standardized handout
干预措施: Control (Other)
Intervention
Experimental
The intervention group will be shown an educational video
干预措施: Intervention (Other)
结局指标
主要结局
Participation Rate
时间窗: Up to 6 weeks
The Ratio of the number of participants to the number of patients asked to join the clinical trial
Survey Completion Rate
时间窗: Up to 6 Weeks
The Ratio of the number of participants who complete the survey to the number of participants overall.
次要结局
- Change in intention to discuss HPV vaccination(Up to 6 weeks)
- Change in social norms and behaviors(Up to 6 weeks)
- Change in Stigma(Up to 6 weeks)
- Change in Health Literacy(Up to 6 weeks)
研究者
Radhika Gogoi
Principal Investigator, Associate Professor
Barbara Ann Karmanos Cancer Institute
研究点 (2)
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