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Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial

INTRODUCTION: Men in sub-Saharan Africa are less likely than women to initiate antiretroviral therapy (ART) and more likely to have longer cycles of disengagement from ART programmes. Treatment interventions that meet the unique needs of men are needed, but they must be scalable. We will test the im...

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Autores principales: Dovel, Kathryn, Balakasi, Kelvin, Hubbard, Julie, Phiri, Khumbo, Nichols, Brooke E, Coates, Thomas J, Kulich, Michal, Chikuse, Elijah, Phiri, Sam, Long, Lawrence C, Hoffman, Risa M, Choko, Augustine T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347494/
https://www.ncbi.nlm.nih.gov/pubmed/37438067
http://dx.doi.org/10.1136/bmjopen-2022-070896
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author Dovel, Kathryn
Balakasi, Kelvin
Hubbard, Julie
Phiri, Khumbo
Nichols, Brooke E
Coates, Thomas J
Kulich, Michal
Chikuse, Elijah
Phiri, Sam
Long, Lawrence C
Hoffman, Risa M
Choko, Augustine T
author_facet Dovel, Kathryn
Balakasi, Kelvin
Hubbard, Julie
Phiri, Khumbo
Nichols, Brooke E
Coates, Thomas J
Kulich, Michal
Chikuse, Elijah
Phiri, Sam
Long, Lawrence C
Hoffman, Risa M
Choko, Augustine T
author_sort Dovel, Kathryn
collection PubMed
description INTRODUCTION: Men in sub-Saharan Africa are less likely than women to initiate antiretroviral therapy (ART) and more likely to have longer cycles of disengagement from ART programmes. Treatment interventions that meet the unique needs of men are needed, but they must be scalable. We will test the impact of various interventions on 6-month retention in ART programmes among men living with HIV who are not currently engaged in care (never initiated ART and ART clients with treatment interruption). METHODS AND ANALYSIS: We will conduct a programmatic, individually randomised, non-blinded, controlled trial. ‘Non-engaged’ men will be randomised 1:1:1 to either a low-intensity, high-intensity or stepped arm. The low-intensity intervention includes one-time male-specific counseling+facility navigation only. The high-intensity intervention offers immediate outside-facility ART initiation+male-specific counselling+facility navigation for follow-up ART visits. In the stepped arm, intervention activities build in intensity over time for those who do not re-engage in care with the following steps: (1) one-time male-specific counselling+facility navigation→(2) ongoing male mentorship+facility navigation→(3) outside-facility ART initiation+male-specific counselling+facility navigation for follow-up ART visits. Our primary outcome is 6-month retention in care. Secondary outcomes include cost-effectiveness and rates of adverse events. The primary analysis will be intention to treat with all eligible men in the denominator and all men retained in care at 6 months in the numerator. The proportions achieving the primary outcome will be compared with a risk ratio, corresponding 95% CI and p value computed using binomial regression accounting for clustering at facility level. ETHICS AND DISSEMINATION: The Institutional Review Board of the University of California, Los Angeles and the National Health Sciences Research Council in Malawi have approved the trial protocol. Findings will be disseminated rapidly in national and international forums and in peer-reviewed journals and are expected to provide urgently needed information to other countries and donors. TRIAL REGISTRATION NUMBER: NCT05137210. DATE AND VERSION: 5 May 2023; version 3.
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spelling pubmed-103474942023-07-15 Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial Dovel, Kathryn Balakasi, Kelvin Hubbard, Julie Phiri, Khumbo Nichols, Brooke E Coates, Thomas J Kulich, Michal Chikuse, Elijah Phiri, Sam Long, Lawrence C Hoffman, Risa M Choko, Augustine T BMJ Open HIV/AIDS INTRODUCTION: Men in sub-Saharan Africa are less likely than women to initiate antiretroviral therapy (ART) and more likely to have longer cycles of disengagement from ART programmes. Treatment interventions that meet the unique needs of men are needed, but they must be scalable. We will test the impact of various interventions on 6-month retention in ART programmes among men living with HIV who are not currently engaged in care (never initiated ART and ART clients with treatment interruption). METHODS AND ANALYSIS: We will conduct a programmatic, individually randomised, non-blinded, controlled trial. ‘Non-engaged’ men will be randomised 1:1:1 to either a low-intensity, high-intensity or stepped arm. The low-intensity intervention includes one-time male-specific counseling+facility navigation only. The high-intensity intervention offers immediate outside-facility ART initiation+male-specific counselling+facility navigation for follow-up ART visits. In the stepped arm, intervention activities build in intensity over time for those who do not re-engage in care with the following steps: (1) one-time male-specific counselling+facility navigation→(2) ongoing male mentorship+facility navigation→(3) outside-facility ART initiation+male-specific counselling+facility navigation for follow-up ART visits. Our primary outcome is 6-month retention in care. Secondary outcomes include cost-effectiveness and rates of adverse events. The primary analysis will be intention to treat with all eligible men in the denominator and all men retained in care at 6 months in the numerator. The proportions achieving the primary outcome will be compared with a risk ratio, corresponding 95% CI and p value computed using binomial regression accounting for clustering at facility level. ETHICS AND DISSEMINATION: The Institutional Review Board of the University of California, Los Angeles and the National Health Sciences Research Council in Malawi have approved the trial protocol. Findings will be disseminated rapidly in national and international forums and in peer-reviewed journals and are expected to provide urgently needed information to other countries and donors. TRIAL REGISTRATION NUMBER: NCT05137210. DATE AND VERSION: 5 May 2023; version 3. BMJ Publishing Group 2023-07-12 /pmc/articles/PMC10347494/ /pubmed/37438067 http://dx.doi.org/10.1136/bmjopen-2022-070896 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle HIV/AIDS
Dovel, Kathryn
Balakasi, Kelvin
Hubbard, Julie
Phiri, Khumbo
Nichols, Brooke E
Coates, Thomas J
Kulich, Michal
Chikuse, Elijah
Phiri, Sam
Long, Lawrence C
Hoffman, Risa M
Choko, Augustine T
Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title_full Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title_fullStr Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title_full_unstemmed Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title_short Identifying efficient linkage strategies for men (IDEaL): a study protocol for an individually randomised control trial
title_sort identifying efficient linkage strategies for men (ideal): a study protocol for an individually randomised control trial
topic HIV/AIDS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347494/
https://www.ncbi.nlm.nih.gov/pubmed/37438067
http://dx.doi.org/10.1136/bmjopen-2022-070896
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