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临床试验/NCT06229353
NCT06229353终止不适用

Developing and Evaluating a Novel Approach to Improve HPV Vaccination Coverage Among High-risk, Under-immunized Adults Via the Emergency Department

University of Alabama at Birmingham1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2024年8月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
34
试验地点
1
主要终点
Number of study participants who receive HPV vaccination at baseline

研究概览

简要总结

To determine if the emergency department (ED) setting offers a viable space for improving HPV vaccination coverage among 18 to 45-year-old adults who have not yet received human papilloma virus (HPV) vaccination or who did not complete the vaccine series. This study will develop, pilot and evaluate an ED-based HPV vaccination protocol and program for ED patients aged 18-26 (for whom catch-up HPV vaccination is routinely recommended by the CDC) and separately for patients aged 27-45 (for whom it may be recommended under shared decision making, SDM).

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
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •aged 18-45 years old
  • •in good functional capacity, as determined by the ED-attending clinician
  • •no known infection with HPV high risk strain types 6, 11, 16 and 18.

排除标准

  • •will not receive vaccine if participants lack mental clarity and if running a fever or in some pain.
  • •Patients aged <18 or > 45 years of age.
  • •Female patients with abnormal HPV results (including those with the high-risk HPV strain types 6, 11, 16, and 18) as determined by a previous PAP smear test or HPV test.
  • •Female patients who are known to be pregnant.
  • •Male patients with known cases of HPV-associated infections will also be excluded from the study

研究组 & 干预措施

Under-immunized Emergency Department adult patients

Adults attending the Emergency Department who are aged 18-45, without previous HPV vaccination history and without previously known infection from HPV high-risk strain, and in good functional capacity.

Eligible participants will receive Gardasil 9 (HPV) vaccination if interested.

干预措施: Gardasil 9 (Biological)

结局指标

主要结局

Number of study participants who receive HPV vaccination at baseline

时间窗: Baseline

HPV vaccination will be administered at the time of the study participant's initial visit (baseline)

Number of study participants who receive HPV vaccination at 2 months

时间窗: 2 months

Number of study participants receiving dose 2 of the HPV vaccination series 2 months after initial study visit

Number of study participants who receive HPV vaccinations at 6 months

时间窗: 6 months

Number of study participants receiving dose 3 of the HPV vaccination series 6 months after initial study visit

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

Andrzej Kulczycki

Associate Professor

University of Alabama at Birmingham

研究点 (1)

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