Department of Social Medicine, School of Medicine, The University of North Carolina at Chapel Hill, 333 South Columbia Street, MacNider Hall, Room #348 / CB #7240, Chapel Hill, NC, 27599-7240, USA.
Institute for Global Health and Infectious Disease, School of Medicine, The University of North Carolina at Chapel Hill, 333 South Columbia Street, MacNider Hall, Room #348 / CB #7240, Chapel Hill, NC, 27599-7240, USA.
BMC Public Health. 2020 Apr 15;20(1):494. doi: 10.1186/s12889-020-08582-z.
HIV testing programs in the United States aim to reach ethnic minority populations who experience high incidence of HIV, yet 40% of African Americans have never been tested for HIV. The objective of this study is to identify community-based strategies to increase testing among African Americans in both urban and rural areas.
This study conducted focus group discussions (FGDs) informed by community-based participatory research principles to examine African American's concerns and ideas around HIV testing and HIV self-testing. Participants included highly affected (i.e., PLWH, MSM, PWID, low-income, teens and young adults) populations from African American communities in North Carolina, aged 15 years and older. We digitally transcribed and analyzed qualitative data using MAXQDA and axial coding to identify emergent themes.
Fifty-two men and women between 15 to 60 years old living in urban (n=41) and rural (n=11) areas of North Carolina participated in focus group discussions. HIV testing barriers differed by HIV testing setting: facility-based, community-based, and HIV self-testing. In community-based settings, barriers included confidentiality concerns. In facility-based settings (e.g., clinics), barriers included negative treatment by healthcare workers. With HIV self-testing, barriers included improper use of self-testing kits and lack of post-test support. HIV testing facilitators included partnering with community leaders, decentralizing testing beyond facility-based sites, and protecting confidentiality.
Findings suggest that HIV testing concerns among African Americans vary by HIV testing setting. African Americans may be willing to test for HIV at community events in public locations if client confidentiality is preserved and use HIV self-testing kits in private if post-test social support and services are provided. These community-identified facilitators may improve African American testing rates and uptake of HIV self-testing kits.
美国的艾滋病毒检测计划旨在覆盖那些艾滋病毒发病率较高的少数族裔人群,但仍有 40%的非裔美国人从未接受过艾滋病毒检测。本研究的目的是确定基于社区的策略,以增加城市和农村地区非裔美国人的检测率。
本研究采用基于社区的参与性研究原则进行焦点小组讨论(FGD),以探讨非裔美国人对艾滋病毒检测和艾滋病毒自我检测的关注和想法。参与者包括来自北卡罗来纳州非裔美国社区的高度受影响人群(即 PLWH、MSM、PWID、低收入人群、青少年和年轻人),年龄在 15 岁及以上。我们使用 MAXQDA 对定性数据进行数字转录和分析,并采用轴向编码来确定新兴主题。
52 名年龄在 15 至 60 岁之间的男性和女性居住在北卡罗来纳州的城市(n=41)和农村(n=11)地区,他们参加了焦点小组讨论。艾滋病毒检测障碍因检测环境而异:机构环境、社区环境和艾滋病毒自我检测。在社区环境中,障碍包括保密性问题。在机构环境(如诊所)中,障碍包括医护人员的负面对待。在艾滋病毒自我检测中,障碍包括自我检测试剂盒使用不当和缺乏检测后支持。艾滋病毒检测促进因素包括与社区领袖合作、将检测分散到机构场所之外,以及保护保密性。
研究结果表明,非裔美国人的艾滋病毒检测关注点因检测环境而异。如果客户的保密性得到保护,非裔美国人可能愿意在公共场合的社区活动中接受艾滋病毒检测,如果在私人场所提供艾滋病毒自我检测试剂盒后社会支持和服务,他们也可能愿意使用自我检测试剂盒。这些社区确定的促进因素可能会提高非裔美国人的检测率和艾滋病毒自我检测试剂盒的使用率。