Participant Perspectives and Experiences Following an Intensively Monitored Antiretroviral Pause in the United States: Results from the AIDS Clinical Trials Group A5345 Biomarker Study.

analytical treatment interruption behavioral sciences intensively monitored antiretroviral pause persons living with HIV social sciences

Journal

AIDS research and human retroviruses
ISSN: 1931-8405
Titre abrégé: AIDS Res Hum Retroviruses
Pays: United States
ID NLM: 8709376

Informations de publication

Date de publication:
06 2022
Historique:
pubmed: 25 3 2022
medline: 10 6 2022
entrez: 24 3 2022
Statut: ppublish

Résumé

The AIDS Clinical Trials Group A5345 study (NCT03001128) included an intensively monitored antiretroviral pause (IMAP), during which participants living with HIV temporarily stopped antiretroviral treatment (ART) in an effort to identify biomarkers that could predict HIV rebound. We evaluated the potential impact of the IMAP on A5345 study participants in the United States by questioning them immediately after the IMAP and at the end of the study. We administered longitudinal sociobehavioral questionnaires to participants following the IMAP when they resumed ART and at the end of the study. We summarized descriptive data from the post-IMAP and end-of-study questionnaires. Open-ended responses were analyzed using conventional content analysis. Reactions to pausing ART involved a mixture of curiosity and satisfaction from contributing to science. All participants indicated adherence with the ART interruption. About half (9/17) of post-IMAP questionnaire respondents reported having sexual partner(s) during the IMAP, and of those, nearly all (8/9) did not find it difficult to use measures to prevent HIV transmission to partners. The majority believed that they benefited from the study, yet some had elevated anxiety following the IMAP and at the end of the study. Most (24/29) respondents who completed the end-of-study questionnaire would recommend the study to other people living with HIV. Our findings underscore the relevance of the psychosocial aspects of participating in studies that involve interruptions of ART. Understanding how participants experience this research is invaluable for informing the design of future research aimed at sustained ART-free virologic suppression.

Identifiants

pubmed: 35323030
doi: 10.1089/AID.2021.0170
pmc: PMC9225827
doi:

Substances chimiques

Anti-Retroviral Agents 0
Biomarkers 0

Banques de données

ClinicalTrials.gov
['NCT03001128']

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

510-517

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI126620
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH126768
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH118120
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH123248
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106701
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH062246
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NIMH NIH HHS
ID : R25 MH067127
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069496
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069412
Pays : United States

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Auteurs

Karine Dubé (K)

Public Health Leadership Program and Health Policy and Management, UNC Gillings School of Global Public Health, Chapel Hill, North Carolina, USA.

Shadi Eskaf (S)

UNC School of Government, Chapel Hill, North Carolina, USA.

Liz Barr (L)

Community Scientific Sub-Committee, AIDS Clinical Trials Group (ACTG), Baltimore, Maryland, USA.

David Palm (D)

Community Scientific Sub-Committee, AIDS Clinical Trials Group (ACTG), Baltimore, Maryland, USA.
Institute of Global Health and Infectious Diseases (IGHID), University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Evelyn Hogg (E)

Social and Scientific Systems, Inc., a DLH Holdings Company, Silver Spring, Maryland, USA.

Jane M Simoni (JM)

Department of Psychology, University of Washington, Seattle, Washington, USA.
Department of Global Health, and Women, and Sexuality Studies, University of Washington, Seattle, Washington, USA.
Department of Gender, Women, and Sexuality Studies, University of Washington, Seattle, Washington, USA.

Jeremy Sugarman (J)

Johns Hopkins Berman Institute for Bioethics, Baltimore, Maryland, USA.

Brandon Brown (B)

Center for Healthy Communities, Department of Social Medicine, Population and Public Health, University of California, Riverside School of Medicine, Riverside, California, USA.

John A Sauceda (JA)

Center for AIDS Prevention Studies (CAPS), Division of Prevention Sciences, University of California, San Francisco, San Francisco, California, USA.

Laney Henley (L)

Public Health Leadership Program and Health Policy and Management, UNC Gillings School of Global Public Health, Chapel Hill, North Carolina, USA.

Steven Deeks (S)

Division of HIV, Infectious Diseases and Global Medicine, University of California, San Francisco, California, USA.

Lawrence Fox (L)

Division of AIDS (DAIDS), National Institute of Health (NIH), Bethesda, Maryland, USA.

Rajesh T Gandhi (RT)

Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA.

Davey Smith (D)

Division of Infectious Diseases and Global Health, University of California, San Diego, California, USA.

Jonathan Z Li (JZ)

Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

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Classifications MeSH