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      A multilevel health system intervention for virological suppression in adolescents and young adults living with HIV in rural Kenya and Uganda (SEARCH-Youth): a cluster randomised trial

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          Summary

          Background

          Social and cognitive developmental events can disrupt care and medication adherence among adolescents and young adults living with HIV in sub-Saharan Africa. We hypothesised that a dynamic multilevel health system intervention helping adolescents and young adults and their providers navigate life-stage related events would increase virological suppression compared with standard care.

          Methods

          We did a cluster randomised, open-label trial of young individuals aged 15–24 years with HIV and receiving care in eligible clinics (operated by the government and with ≥25 young people receiving care) in rural Kenya and Uganda. After clinic randomisation stratified by region, patient population, and previous participation in the SEARCH trial, participants in intervention clinics received life-stage-based assessment at routine visits, flexible clinic access, and rapid viral load feedback. Providers had a secure mobile platform for interprovider consultation. The control clinics followed standard practice. The primary, prespecified endpoint was virological suppression (HIV RNA <400 copies per mL) at 2 years of follow-up among participants who enrolled before Dec 1, 2019, and received care at the study clinics. This trial is registered with ClinicalTrials.gov, NCT03848728, and is closed to recruitment.

          Findings

          28 clinics were enrolled and randomly assigned (14 control, 14 intervention) in January, 2019. Between March 14, 2019, and Nov 26, 2020, we recruited 1988 participants at the clinics, of whom 1549 were included in the analysis (785 at intervention clinics and 764 at control clinics). The median participant age was 21 years (IQR 19–23) and 1248 (80·6%) of 1549 participants were female. The mean proportion of participants with virological suppression at 2 years was 88% (95% CI 85–92) for participants in intervention clinics and 80% (77–84) for participants in control clinics, equivalent to a 10% beneficial effect of the intervention (risk ratio [RR] 1·10, 95% CI 1·03–1·16; p=0·0019). The intervention resulted in increased virological suppression within all subgroups of sex, age, and care status at baseline, with greatest improvement among those re-engaging in care (RR 1·60, 95% CI 1·00–2·55; p=0·025).

          Interpretation

          Routine and systematic life-stage-based assessment, prompt adherence support with rapid viral load testing, and patient-centred, flexible clinic access could help bring adolescents and young adults living with HIV closer towards a goal of universal virological suppression.

          Funding

          Eunice Kennedy Shriver National Institute of Child Health and Human Development, US National Institutes of Health.

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          Most cited references30

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          Adolescence: a foundation for future health

          Adolescence is a life phase in which the opportunities for health are great and future patterns of adult health are established. Health in adolescence is the result of interactions between prenatal and early childhood development and the specific biological and social-role changes that accompany puberty, shaped by social determinants and risk and protective factors that affect the uptake of health-related behaviours. The shape of adolescence is rapidly changing-the age of onset of puberty is decreasing and the age at which mature social roles are achieved is rising. New understandings of the diverse and dynamic effects on adolescent health include insights into the effects of puberty and brain development, together with social media. A focus on adolescence is central to the success of many public health agendas, including the Millennium Development Goals aiming to reduce child and maternal mortality and HIV/AIDS, and the more recent emphases on mental health, injuries, and non-communicable diseases. Greater attention to adolescence is needed within each of these public health domains if global health targets are to be met. Strategies that place the adolescent years centre stage-rather than focusing only on specific health agendas-provide important opportunities to improve health, both in adolescence and later in life. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Pragmatic Trials.

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              Simple sample size calculation for cluster-randomized trials.

              Cluster-randomized trials, in which health interventions are allocated randomly to intact clusters or communities rather than to individual subjects, are increasingly being used to evaluate disease control strategies both in industrialized and in developing countries. Sample size computations for such trials need to take into account between-cluster variation, but field epidemiologists find it difficult to obtain simple guidance on such procedures. In this paper, we provide simple formulae for sample size determination for both unmatched and pair-matched trials. Outcomes considered include rates per person-year, proportions and means. For simplicity, formulae are expressed in terms of the coefficient of variation (SD/mean) of cluster rates, proportions or means. Guidance is also given on the estimation of this value, with or without the use of prior data on between-cluster variation. The methods are illustrated using two case studies: an unmatched trial of the impact of impregnated bednets on child mortality in Kenya, and a pair-matched trial of improved sexually-transmitted disease (STD) treatment services for HIV prevention in Tanzania.
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                Author and article information

                Journal
                101645355
                43213
                Lancet HIV
                Lancet HIV
                The lancet. HIV
                2405-4704
                2352-3018
                1 June 2024
                August 2023
                07 June 2024
                : 10
                : 8
                : e518-e527
                Affiliations
                Department of Pediatrics (Prof T Ruel MD), Division of HIV, Infectious Diseases and Global Medicine, Department of Medicine (D Black BA, J Schrom MPH, Prof D Havlir MD), Department of Epidemiology and Biostatistics (Prof E Charlebois PhD, S B Shade PhD), and Department of Obstetrics, Gynecology & Reproductive Sciences (Prof C Camlin PhD), University of California, San Francisco, San Francisco, CA, USA; Infectious Diseases Research Collaboration, Kampala, Uganda (F Mwangwa MSc, B Nzarubara MSc, B Kamugisha MSc, J Kabami MPH, H N Atuhaire BMLS); Division of Biostatistics, School of Public Health, University of California, Berkeley, CA, USA (L B Balzer PhD, J Schwab MSc); Kenya Medical Research Institute, Kisumu, Kenya (J Ayieko PhD, M Nyabuti MBchB, W E Mugoma MSc, F Opel BS, G Agengo BSc, Prof E Bukusi PhD); Department of Psychiatry (J Nakigudde PhD) and Department of Medicine (Prof M R Kamya PhD), Makerere University College of Health Sciences, Kampala, Uganda; Department of Biostatistics, University of Washington, Seattle, WA, USA (J Peng MS); Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA (B G Kapogiannis MD)
                Author notes

                Contributors

                FM, EC, JA, WEM, FO, DB, JP, JK, MRK, CC, SBS, DH, and TR conceptualised and designed the study. All authors participated in study operations, data collection, and design modifications. LBB, JA, MN, WEM, JK, BK, and SBS did the statistical analysis, with input from JP, JSchr, JSchw, TR, FM, and DH. TR wrote the first draft of the manuscript, with input from FM, LBB, and DH. LBB, WEM, BK, FM, and TR directly accessed and verified the study data. All authors reviewed the initial draft and approved the final manuscript. All authors had full access to all the data in the study and had final responsibility for the decision to submit for publication.

                [*]

                Joint first authors

                Correspondence to: Prof Theodore Ruel, Department of Pediatrics, University of California, San Francisco, CA 94158-0434, USA, theodore.ruel@ 123456ucsf.edu
                Article
                NIHMS1998338
                10.1016/S2352-3018(23)00118-2
                11158418
                37541706
                733d586c-523b-4ef1-8656-ea937dbe8f02

                This is an Open Access article under the CC BY 4.0 license.

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