Integrating hypertension detection and management in HIV care in South Africa: protocol for a stepped-wedged cluster randomized effectiveness-implementation hybrid trial.

Karla I Galaviz, Shivani A Patel, Mark J Siedner, Charles W Goss, Siphamandla B Gumede, Leslie C Johnson, Claudia E Ordóñez, Michael Laxy, Kerstin Klipstein-Grobusch, Martin Heine, Mary Masterson, Aaloke Mody, W D Francois Venter, Vincent C Marconi, Mohammed K Ali, Samanta T Lalla-Edward
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Abstract

Background: HIV clinical guidelines recommend hypertension detection and management to lower cardiovascular disease risk, but these have not been effectively implemented for people living with HIV (PWH). Addressing this implementation gap requires community-engaged implementation studies focused on addressing implementation barriers specific to the HIV care context.

Methods: This protocol describes a type 2 effectiveness-implementation hybrid study conducted in nine primary care clinics in Johannesburg. The study will evaluate the effect of implementation strategies on guideline-recommended blood pressure assessment and management in HIV clinics and the effects of assessment/management on patient blood pressure. A stepped-wedge, cluster randomized study design was used to randomize clinics to the time at which they receive the implementation strategies and patient intervention. The implementation strategies tested include identifying and preparing care champions, changing record systems, conducting ongoing training, providing audit and feedback, and changing the physical structure/equipment. The patient intervention tested includes detection of elevated blood pressure, educational materials, lifestyle modification advice, and medication where needed. Implementation outcomes include adoption, fidelity (co-primary outcome), cost, and maintenance of the blood pressure assessment protocol in participating clinics, while patient outcomes include reach, effectiveness (co-primary outcome), and long-term effects of the intervention on patient blood pressure. These will be assessed via direct observation, study records, staff logs, medical chart reviews, and patient and healthcare worker surveys. To examine effects on the implementation (intervention fidelity) and effectiveness (patient blood pressure changes) co-primary outcomes, we will use the standard Hussey and Hughes model for analysis of stepped-wedge designs which includes fixed effects for both interventions and time periods, and a random effect for sites. Finally, we will examine the costs for the implementation strategies, healthcare worker time, and patient-facing intervention materials, as well as the cost-effectiveness and cost-utility of the intervention using study records, patient surveys, and a time and motion assessment.

Discussion: This study will address knowledge gaps around implementation of cardiovascular disease preventive practices in HIV care in South Africa. In doing so, it will provide a dual opportunity to promote evidence-based care in the South African HIV care context and help refine implementation research methods to better serve HIV populations globally.

Trial registration: ClinicalTrials.gov: NCT05846503. Registered on May 6, 2023. https://classic.

Clinicaltrials: gov/ct2/show/NCT05846503 .

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将高血压检测和管理纳入南非艾滋病护理:阶梯式分组随机有效性-实施混合试验方案。
背景:艾滋病临床指南建议通过检测和管理高血压来降低心血管疾病风险,但这些建议并未在艾滋病感染者(PWH)中得到有效实施。要解决这一实施差距,需要开展社区参与的实施研究,重点解决艾滋病护理背景下特有的实施障碍:本方案介绍了在约翰内斯堡九家初级保健诊所开展的第二类有效性-实施混合研究。该研究将评估在 HIV 诊所实施指南推荐的血压评估和管理策略的效果,以及评估/管理对患者血压的影响。该研究采用阶梯式楔形分组随机研究设计,将诊所随机分配到接受实施策略和患者干预的时间。所测试的实施策略包括确定和培养护理标兵、改变记录系统、开展持续培训、提供审核和反馈以及改变物理结构/设备。测试的患者干预措施包括检测血压升高、教育材料、生活方式调整建议以及必要的药物治疗。实施结果包括参与诊所对血压评估方案的采用情况、忠实度(共同主要结果)、成本和维护情况,而患者结果包括干预措施的覆盖范围、有效性(共同主要结果)和对患者血压的长期影响。这些将通过直接观察、研究记录、员工日志、病历审查以及患者和医护人员调查进行评估。为了考察干预的实施效果(干预的忠实性)和有效性(患者血压的变化)这两个共同的主要结果,我们将使用标准的 Hussey 和 Hughes 模型来分析阶梯式楔形设计,该模型包括干预和时间段的固定效应以及地点的随机效应。最后,我们将利用研究记录、患者调查和时间与运动评估,检查实施策略、医护人员时间和面向患者的干预材料的成本,以及干预的成本效益和成本效用:本研究将填补南非在艾滋病护理中实施心血管疾病预防措施方面的知识空白。在此过程中,它将提供一个双重机会,既能在南非艾滋病护理中推广循证护理,又能帮助完善实施研究方法,从而更好地为全球艾滋病人群服务:试验注册:ClinicalTrials.gov:NCT05846503.注册日期为 2023 年 5 月 6 日。https://classic.Clinicaltrials: gov/ct2/show/NCT05846503 。
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