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临床试验/NCT06178549
NCT06178549已完成不适用

Feasibility and Effectiveness of HPV Self-Sampling for Cervical Cancer Screening Among Women Seeking Health Care At a Safety Net Hospital Emergency Room

Baylor College of Medicine2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年11月15日最近更新:
适应症

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
HPV self-sampling completion

研究概览

简要总结

The goal of this study is to develop and evaluate an evidence-based public health intervention using HPV self-sampling approach in an opportunistic setting to increase cervical cancer screening among screening non-attendees, particularly those uninsured or underinsured, who use emergency services to access medical care. The proposed pilot study will examine the feasibility and efficacy of HPV self-sampling among women at a safety net hospital emergency room. Participant recruitment and self-sample will take place in the waiting rooms in the ER. All women sitting in the waiting room will serve as the source population for the study and will be approached and invited to participate in the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Eligible participants are women ages 25 years to 65 years, with a cervix, presenting in the waiting areas at the Ben Taub General Hospital Emergency Department

排除标准

  • Women under 25 years or older than 65 years of age,
  • self-reported current pregnancy,
  • self-reported history of cervical cancer,
  • past hysterectomy,
  • had Pap Smear within past 3 years or HPV/Pap co-test within past 5 years.

结局指标

主要结局

HPV self-sampling completion

时间窗: 1 day

Participation rate for self-sample HPV testing (percent of eligible women who complete self-sampling).

次要结局

  • HPV self-sampling acceptability(1 day)
  • Attendance for cervical cancer screening among HR-HPV positive women(6 months)

研究者

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

Aaron Peter Thrift

Associate Professor

Baylor College of Medicine

研究点 (2)

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