跳至主要内容
临床试验/NCT04614155
NCT04614155已完成不适用

Texas State HPV Self-Collection Pilot Study

M.D. Anderson Cancer Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年8月27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
40
试验地点
2
主要终点
Human papillomavirus (HPV) self-collection uptake rate

研究概览

简要总结

This trial studies if Project Self can improve the rate of cervical cancer screening in Hispanic and African American women living in Houston, Texas. Project Self may help to improve cervical cancer screening rates by providing human papillomavirus (HPV) self-collection kits, education, counseling, and navigation.

详细描述

PRIMARY OBJECTIVES:

I. To examine the feasibility of conducting an education intervention trial regarding cervical cancer screening among women of Hispanic and African American origin living in public housing units in Houston, Texas.

SECONDARY OBJECTIVES:

I. Document cervical screening associated knowledge, attitudes and practices among Hispanic and African American women living in public housing units in Houston, Texas at pre- and post-health education.

II. Document Pap smear screening rate in last 3 years among participants. III. Document HPV positive rate among participants.

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
30 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Self-identify as African American or Hispanic women.
  • Valid home address reflective of residence in the participating housing development(s) at least 50% of the time.
  • Functioning telephone number.
  • Speak and read English or Spanish.

排除标准

  • Self-reported hysterectomy.
  • Self-reported personal history of cancer/cancer diagnosis.
  • Self-reported as pregnant.
  • Another household member is enrolled in this protocol.

结局指标

主要结局

Human papillomavirus (HPV) self-collection uptake rate

时间窗: Up to 2 weeks after health education session

Defined as the proportion of the participants who consent to the study and receive an HPV self-collection kit complete the self-collection and return the sample to the lab or research staff member or community health worker within timeline.

Participant consent rate

时间窗: Up to 1 month

次要结局

  • HPV positive proportion(Up to 1 month)
  • Cervical screening associated knowledge, attitudes and practices score(Up to 1 month)
  • Participants' self-reported Pap smear screening rate in last 3 years(Up to 1 month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验