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Implementation of a Provider-Focused Intervention for Maximizing HPV Vaccine Uptake in Young Cancer Survivors receiving Follow-Up Care in Pediatric Oncology Practices: A Cluster-Randomized Trial

Implementation of a Provider-Focused Intervention for Maximizing HPV Vaccine Uptake in Young Cancer Survivors receiving Follow-Up Care in Pediatric Oncology Practices: A Cluster-Randomized Trial
实施以提供者为中心的干预措施,以最大限度地提高在儿科肿瘤实践中接受后续护理的年轻癌症幸存者的 HPV 疫苗接种:整群随机试验
批准号:
10076219
负责人:
James Klosky
金额:
$185.69万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-09-18 至 2023-08-31

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中文摘要
翻译
项目摘要/摘要 儿童癌症幸存者罹患新癌症(如宫颈癌和肛门癌)的风险很高。 由持续感染人乳头瘤病毒(HPV)引起。存在一种有效的疫苗可以预防 这些癌症,但年轻的癌症幸存者对HPV疫苗的接受率很低(不到四分之一 接种疫苗)。最常见的是缺乏医疗保健提供者对HPV疫苗的推荐 癌症幸存者未能接种HPV疫苗的原因。在增加HPV方面最成功的策略 普通人群接种疫苗的重点是提高卫生保健提供者对HPV的了解 疫苗,增强医疗保健提供者向年轻人有效推荐疫苗所需的技能 人们及其父母,并减少接种疫苗的障碍。这项拟议的研究将评估 循证干预的有效性和实施,适用于医疗保健提供者 在儿科肿瘤诊所,增加年轻癌症幸存者(9至17岁)的HPV疫苗接种率 年龄和至少一年未接受治疗)。如果干预措施在改善和维持增长方面有效 在年轻癌症幸存者中对HPV疫苗的接受情况,这项研究将有助于提供必要的重要信息 继续测试干预在儿科肿瘤学实践中的广泛使用。这项建议 研究旨在通过预防改善癌症幸存者的医疗保健服务和临床结局 HPV相关癌症,这是国家癌症研究所的高度优先研究领域。
英文摘要
PROJECT SUMMARY/ABSTRACT Childhood cancer survivors are at high risk for developing new cancers (such as cervical and anal cancer) caused by persistent infection with the human papillomavirus (HPV). An effective vaccine exists that can prevent these cancers, but uptake of the HPV vaccine is low among young cancer survivors (fewer than 1 in 4 have received the vaccine). Lack of a healthcare provider recommendation for the HPV vaccine is the most common reason that cancer survivors fail to get the HPV vaccine. Strategies that are most successful in increasing HPV vaccine uptake in the general population focus on improving healthcare provider knowledge about the HPV vaccine, enhancing the skills that healthcare providers need to effectively recommend the vaccine to young people and their parents, and reducing barriers to receiving the vaccine. This proposed research will evaluate the effectiveness and implementation of an evidence-based intervention, adapted for use by healthcare providers in pediatric oncology clinics, to increase the uptake of HPV vaccine among young cancer survivors (9 to 17 years of age and at least one year off-therapy). If the intervention is effective in improving and sustaining increased uptake of the HPV vaccine in young cancer survivors, this study will contribute important information needed to move forward with testing the widespread use of the intervention in pediatric oncology practices. This proposed research addresses improving healthcare delivery and clinical outcomes for cancer survivors through prevention of HPV-associated cancers, which are high-priority research areas for the National Cancer Institute.
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