Blizard Institute, Queen Mary University, London, UK.
SHARE Collaborative, Queen Mary University, London, UK.
BMJ Open. 2023 Jul 9;13(7):e070666. doi: 10.1136/bmjopen-2022-070666.
Cabotegravir and rilpivirine (CAB+RPV long-acting (LA)) is recommended as a treatment for HIV-1 allowing people living with HIV to receive 2 monthly injectable treatment, rather than daily pills. Providing injectable therapy in a system designed to provide and manage study participants on oral treatments poses logistical challenges namely how resources are used to accommodate patient preference within constrained health economies with capacity limitations. In this pragmatic multicentre study, we aim to understand the implementation of CAB-RPV-LA administration in two settings via mixed methods to explore perspectives of participants and the clinical team delivering CAB+RPV LA.
Women, racially minoritised people and older people are chronically under-represented in HIV clinical trials so the ILANA trial has set recruitment caps to ensure recruitment of 50% women, 50% ethnically diverse people and 30% over 50 years of age to include a more representative study population. Using a mixed-methods approach, the primary objective is to identify and evaluate the critical implementation strategies for CAB+RPV LA in both hospital and community settings. Secondary objectives include evaluating feasibility and acceptability of CAB+RPV LA administration at UK clinics and community settings from the perspective of HIV care providers, nurses and representatives at community sites, evaluating barriers to implementation, the utility of implementation strategies and adherence.
Ethical approval has been obtained from the Health Research Authority Research Ethics Committee (REC reference: 22/PR/0318). The dissemination strategy has been formulated with the SHARE Collaborative Community Advisory Board to maximise the impact of this work on clinical care and policy. This strategy draws on and leverages existing resources within the participating organisations, such as their academic infrastructure, professional relationships and community networks. The strategy will leverage the Public Engagement Team and press office to support dissemination of findings.
NCT05294159.
卡博特韦/利匹韦林(CAB+RPV 长效[LA])被推荐作为治疗 HIV-1 的方法,使 HIV 感染者能够接受每月 2 次注射治疗,而不是每天服用药丸。在旨在提供和管理口服治疗研究参与者的系统中提供注射疗法,带来了后勤方面的挑战,即如何在资源有限的卫生经济体中,根据能力限制,利用资源来满足患者的偏好。在这项实用的多中心研究中,我们旨在通过混合方法了解两种环境下 CAB-RPV-LA 给药的实施情况,以探索参与者和提供 CAB+RPV LA 的临床团队的观点。
女性、少数族裔和老年人在 HIV 临床试验中一直代表性不足,因此 ILANA 试验设定了招募上限,以确保招募 50%的女性、50%的不同种族人群和 30%的 50 岁以上人群,以纳入更具代表性的研究人群。本研究采用混合方法,主要目的是确定和评估 CAB+RPV LA 在医院和社区环境中的关键实施策略。次要目标包括从 HIV 护理提供者、护士和社区机构代表的角度评估 CAB+RPV LA 在英国诊所和社区环境中的可行性和可接受性,评估实施障碍、实施策略的效用和依从性。
已从健康研究管理局研究伦理委员会(REC 参考号:22/PR/0318)获得伦理批准。传播策略是与 SHARE 协作社区咨询委员会共同制定的,以最大限度地提高这项工作对临床护理和政策的影响。该策略利用并利用参与组织的现有资源,如他们的学术基础设施、专业关系和社区网络。该策略将利用公众参与团队和新闻办公室来支持传播研究结果。
NCT05294159。