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一项促进性少数群体和性别少数群体对新冠病毒疾病的认识、保护行为并减轻大流行困扰的电子健康干预措施:一项随机对照试验(#安全之手安全之心)方案

An eHealth Intervention for Promoting COVID-19 Knowledge and Protective Behaviors and Reducing Pandemic Distress Among Sexual and Gender Minorities: Protocol for a Randomized Controlled Trial (#SafeHandsSafeHearts).

作者信息

Newman Peter A, Chakrapani Venkatesan, Williams Charmaine, Massaquoi Notisha, Tepjan Suchon, Roungprakhon Surachet, Akkakanjanasupar Pakorn, Logie Carmen, Rawat Shruta

机构信息

Factor-Inwentash Faculty of Social Work, University of Toronto, Toronto, ON, Canada.

Centre for Sexuality and Health Research and Policy, Chennai, India.

出版信息

JMIR Res Protoc. 2021 Dec 10;10(12):e34381. doi: 10.2196/34381.

Abstract

BACKGROUND

Existing data on COVID-19 disparities among vulnerable populations portend excess risk for lesbian, gay, bisexual, transgender (LGBT) and other persons outside of heteronormative and cisgender identities (ie, LGBT+). Owing to adverse social determinants of health, including pervasive HIV and sexual stigma, harassment, violence, barriers in access to health care, and existing health and mental health disparities, sexual and gender minorities in India and Thailand are at disproportionate risk for SARS-CoV-2 infection and severe disease. Despite global health disparities among LGBT+ populations, there is a lack of coordinated, community-engaged interventions to address the expected excess burden of COVID-19 and public health-recommended protective measures.

OBJECTIVE

We will implement a randomized controlled trial (RCT) to evaluate the effectiveness of a brief, peer-delivered eHealth intervention to increase COVID-19 knowledge and public health-recommended protective behaviors, and reduce psychological distress among LGBT+ people residing in Bangkok, Thailand, and Mumbai, India. Subsequent to the RCT, we will conduct exit interviews with purposively sampled subgroups, including those with no intervention effect.

METHODS

SafeHandsSafeHearts is a 2-site, parallel waitlist-controlled RCT to test the efficacy of a 3-session, peer counselor-delivered eHealth intervention based on motivational interviewing and psychoeducation. The study methods, online infrastructure, and content were pilot-tested with LGBT+ individuals in Toronto, Canada, before adaptation and rollout in the other contexts. The primary outcomes are COVID-19 knowledge (index based on US Centers for Disease Control and Prevention [CDC] items), protective behaviors (index based on World Health Organization and US CDC guidelines), depression (Patient Health Questionnaire-2), and anxiety (Generalized Anxiety Disorder-2). Secondary outcomes include loneliness, COVID-19 stress, and intended care-seeking. We will enroll 310 participants in each city aged 18 years and older. One-third of the participants will be cisgender gay, bisexual, and other men who have sex with men; one-third will be cisgender lesbian, bisexual, and other women who have sex with women; and one-third will be transfeminine, transmasculine, and gender nonbinary people. Participants will be equally stratified in the immediate intervention and waitlist control groups. Participants are mainly recruited from online social media accounts of community-based partner organizations. They can access the intervention on a computer, tablet, or mobile phone. SafeHandsSafeHearts involves 3 sessions delivered weekly over 3 successive weeks. Exit interviews will be conducted online with 3 subgroups (n=12 per group, n=36 in each city) of purposively selected participants to be informed by RCT outcomes and focal populations of concern.

RESULTS

The RCT was funded in 2020. The trials started recruitment as of August 1, 2021, and all RCT data collection will likely be completed by January 31, 2022.

CONCLUSIONS

The SafeHandsSafeHearts RCT will provide evidence about the effectiveness of a brief, peer-delivered eHealth intervention developed for LGBT+ populations amid the COVID-19 pandemic. If the intervention proves effective, it will provide a basis for future scale-up in India and Thailand, and other low- and middle-income countries.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04870723; https://clinicaltrials.gov/ct2/show/NCT04870723.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/34381.

摘要

背景

关于弱势群体中新冠病毒疾病差异的现有数据表明,女同性恋、男同性恋、双性恋、跨性别者(LGBT)以及其他非异性恋和顺性别身份的人群(即LGBT+)面临更高风险。由于不良的社会健康决定因素,包括普遍存在的艾滋病毒和性污名、骚扰、暴力、获得医疗保健的障碍以及现有的健康和心理健康差异,印度和泰国的性少数群体和性别少数群体感染新冠病毒和罹患重症的风险不成比例地高。尽管LGBT+人群存在全球健康差异,但缺乏协调一致的、社区参与的干预措施来应对预计的新冠病毒疾病额外负担以及公共卫生建议的防护措施。

目的

我们将开展一项随机对照试验(RCT),以评估一项简短的、由同伴提供的电子健康干预措施的有效性,该干预措施旨在增加居住在泰国曼谷和印度孟买的LGBT+人群的新冠病毒疾病知识和公共卫生建议的防护行为,并减轻其心理困扰。在随机对照试验之后,我们将对有目的抽样的亚组进行退出访谈,包括那些没有干预效果的亚组。

方法

“安全之手,安全之心”是一项在两个地点开展的、平行的等待名单对照随机对照试验,旨在测试基于动机性访谈和心理教育的、由同伴咨询师提供的为期3节的电子健康干预措施的效果。在适应并推广到其他环境之前,该研究方法、在线基础设施和内容在加拿大多伦多的LGBT+个体中进行了预试验。主要结局指标包括新冠病毒疾病知识(基于美国疾病控制与预防中心[CDC]项目的指数)、防护行为(基于世界卫生组织和美国疾病控制与预防中心指南的指数)以及抑郁(患者健康问卷-2)和焦虑(广泛性焦虑障碍-2)。次要结局指标包括孤独感、新冠病毒疾病压力以及寻求医疗护理的意向。我们将在每个城市招募310名18岁及以上的参与者。三分之一的参与者将是顺性别男同性恋、双性恋以及其他男男性行为者;三分之一将是顺性别女同性恋、双性恋以及其他女女性行为者;三分之一将是跨女性、跨男性以及性别非二元者。参与者将在即时干预组和等待名单对照组中进行同等分层。参与者主要从基于社区的伙伴组织的在线社交媒体账户中招募。他们可以通过计算机、平板电脑或手机访问该干预措施。“安全之手,安全之心”包括连续3周每周进行1节的课程。将对有目的选择的参与者的3个亚组(每组n = 12,每个城市共n = 36)进行在线退出访谈,以便根据随机对照试验结果和关注的重点人群提供信息。

结果

该随机对照试验于2020年获得资助。试验于2021年8月1日开始招募,所有随机对照试验数据收集可能于2022年1月31日前完成。

结论

“安全之手,安全之心”随机对照试验将提供证据,证明在新冠病毒疾病大流行期间为LGBT+人群开发的简短的、由同伴提供的电子健康干预措施的有效性。如果该干预措施被证明有效,将为未来在印度、泰国以及其他低收入和中等收入国家扩大规模提供依据。

试验注册

ClinicalTrials.gov NCT04870723;https://clinicaltrials.gov/ct2/show/NCT04870723。

国际注册报告识别码(IRRID):DERR1-10.2196/34381。

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