Acceptability of serosurveys in southern Zambia: data collector and caregiver perspectives.

Andrea C Carcelen, Rupali J Limaye, Simon Mutembo, Mutinta Hamahuwa, Philip E Thuma, William J Moss, Kyla Hayford
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引用次数: 0

Abstract

Background: Factors associated with whether individuals choose to participate in serosurveys are not well understood. Understanding perceptions from multiple perspectives, including the perspectives of both data collectors and participants, through a holistic model such as the socio-ecological model contextualizes individual, interpersonal, and structural level influences on survey research participation. We used a multiple methods approach to characterize reasons for serosurvey participation in communities in Southern Province, Zambia where a serosurvey was conducted in 2016.

Methods: The first phase conducted focus group discussions and in-depth interviews with 24 data collectors who participated in a measles-rubella serosurvey in 2016. The second phase surveyed 34 caregivers at health facilities to identify barriers and facilitators to serosurvey participation. Emergent themes were then classified into a socio-ecological model using individual, interpersonal, and structural level constructs.

Results: Common themes emerged from data collectors as well as caregivers surveyed. At the individual level, providing incentives was a facilitator, and some religious beliefs were described as a barrier to serosurvey participation. At the interpersonal level, family dynamics and community peer influences could help or hinder serosurvey participation. Community health workers were consistently named as facilitators of participation. At the structural level, concerns about specimen collection, who was selected for serosurveys, and not receiving test results arose as potential barriers. The most frequently reported facilitator was provision of information about the purpose of the serosurvey (85% of respondents). The most frequently reported barrier was lack of clarity regarding use of their blood specimen (53% of respondents). For specimen collection type, caregivers consistently preferred finger prick blood collection over both venous blood draw and oral swabs.

Conclusion: Serosurvey participation was deemed acceptable to most study participants. The socio-ecological model revealed barriers and facilitators for participation to guide strategies to improve participation which can be applied to ongoing serosurveys for SARS-CoV-2. Serosurveys should continue to develop engagement plans to provide information about blood collection ahead of the serosurvey and communicate the objectives of such studies through trusted sources such as community health workers and traditional leaders.

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赞比亚南部服务调查的可接受性:数据收集者和护理者的观点。
背景:与个体是否选择参加血清调查相关的因素尚不清楚。通过社会生态模型等整体模型,从多个角度(包括数据收集者和参与者的角度)理解感知,将个人、人际和结构层面对调查研究参与的影响置于背景中。2016年,我们在赞比亚南部省份开展了一项血清调查,我们使用了多种方法来描述社区参与血清调查的原因。方法:第一阶段对参与2016年麻疹-风疹血清调查的24名数据采集人员进行焦点小组讨论和深度访谈。第二阶段对卫生机构的34名护理人员进行了调查,以确定参与服务调查的障碍和促进因素。然后,使用个人、人际和结构层次结构将新兴主题分类为社会生态模型。结果:共同的主题出现从数据收集和护理人员调查。在个人一级,提供奖励是一个促进因素,一些宗教信仰被描述为参与服务调查的障碍。在人际层面上,家庭动态和社区同伴影响可以帮助或阻碍服务调查的参与。社区卫生工作者一直被称为参与的促进者。在结构层面上,对标本收集的担忧,选择谁进行血清调查,以及没有收到测试结果,成为潜在的障碍。最常报告的促进因素是提供有关血清调查目的的信息(85%的受访者)。最常报告的障碍是其血液标本的使用不明确(53%的答复者)。对于标本采集类型,护理人员一贯倾向于手指刺血采集,而不是静脉血采集和口腔拭子采集。结论:大多数研究参与者认为可以接受参与血清调查。社会生态模型揭示了参与的障碍和促进因素,以指导提高参与度的战略,这些战略可应用于正在进行的SARS-CoV-2血清调查。血清调查应继续制定参与计划,在血清调查之前提供有关采血的信息,并通过社区卫生工作者和传统领导人等可信赖的来源宣传这类研究的目标。
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来源期刊
Discover Social Science and Health
Discover Social Science and Health intersection of health and social sciences-
CiteScore
0.60
自引率
0.00%
发文量
21
审稿时长
22 days
期刊介绍: Discover Social Science and Health is an interdisciplinary, international journal that publishes papers at the intersection of the social and biomedical sciences. Papers should integrate, in both theory and measures, a social perspective (reflecting anthropology, criminology, economics, epidemiology, policy, sociology, etc) and a concern for health (mental and physical). Health, broadly construed, includes biological and other indicators of overall health, symptoms, diseases, diagnoses, treatments, treatment adherence, and related concerns. Drawing on diverse, sound methodologies, submissions may include reports of new empirical findings (including important null findings) and replications, reviews and perspectives that construe prior research and discuss future research agendas, methodological research (including the evaluation of measures, samples, and modeling strategies), and short or long commentaries on topics of wide interest. All submissions should include statements of significance with respect to health and future research. Discover Social Science and Health is an Open Access journal that supports the pre-registration of studies. Topics Papers suitable for Discover Social Science and Health will include both social and biomedical theory and data. Illustrative examples of themes include race/ethnicity, sex/gender, socioeconomic, geographic, and other social disparities in health; migration and health; spatial distribution of risk factors and access to healthcare; health and social relationships; interactional processes in healthcare, treatments, and outcomes; life course patterns of health and treatment regimens; cross-national patterns in health and health policies; characteristics of communities and neighborhoods and health; social networks and treatment adherence; stigma and disease progression; methodological studies including psychometric properties of measures frequently used in health research; and commentary and analysis of key concepts, theories, and methods in studies of social science and biomedicine. The journal welcomes submissions that draw on biomarkers of health, genetically-informed and neuroimaging data, psychophysiological measures, and other forms of data that describe physical and mental health, access to health care, treatment, and related constructs.
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