Long-Term Effect of Group Support Psychotherapy on Depression and HIV Treatment Outcomes: Secondary Analysis of a Cluster Randomized Trial in Uganda.


Journal

Psychosomatic medicine
ISSN: 1534-7796
Titre abrégé: Psychosom Med
Pays: United States
ID NLM: 0376505

Informations de publication

Date de publication:
01 10 2022
Historique:
pubmed: 27 9 2022
medline: 12 10 2022
entrez: 26 9 2022
Statut: ppublish

Résumé

We aimed to determine the effect of group support psychotherapy (GSP) compared with group HIV education (GHE) on depression and HIV treatment outcomes 24 months after treatment. We further aimed to investigate the mediating role of depression and antiretroviral therapy (ART) adherence in the relationship between GSP and viral load suppression. Thirty HIV clinics across three districts were randomly assigned to deliver either GSP or GHE for depression. Depression and optimal (≥95%) ART adherence was assessed at baseline and 6, 12, 18, and 24 months after treatment. Viral load was drawn from the medical charts at baseline and 12 and 24 months after treatment. Multilevel mixed-effects regression models and generalized structural equation modeling were used to estimate 24-month outcomes and mediation effects. Participants ( N = 1140) were enrolled from HIV clinics offering either GSP ( n = 578 [51%]) or GHE ( n = 562 [49%]). Fewer GSP than GHE participants met the criteria for depression at 24 months after treatment (1% versus 25%; adjusted odds ratio [aOR] = 0.002, 95% confidence interval [CI] = 0.0002-0.018). More GSP than GHE participants reported optimal (≥95%) ART adherence (96% versus 88%; aOR = 20.88, 95% CI = 5.78-75.33) and improved viral suppression (96% versus 88%; aOR = 3.38, 95% CI = 1.02-11.02). The indirect effects of GSP through sequential reduction in depression and improvement in ART adherence at 12 months may partially explain the higher viral suppression rates at 24 months in GSP than GHE groups. In settings where the HIV epidemic persists, depression treatment with GSP may be critical for optimal HIV treatment outcomes.Trial Registration: The Pan African Clinical Trials Registry, number PACTR201608001738234.

Identifiants

pubmed: 36162067
doi: 10.1097/PSY.0000000000001128
pii: 00006842-202210000-00008
pmc: PMC9553261
mid: NIHMS1830942
doi:

Substances chimiques

Anti-HIV Agents 0

Banques de données

PACTR
['PACTR201608001738234']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

914-923

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010937
Pays : United States

Informations de copyright

Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Psychosomatic Society.

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Auteurs

Etheldreda Nakimuli-Mpungu (E)

From the Department of Psychiatry, College of Health Sciences (Nakimuli-Mpungu, Seggane), Makerere University, Kampala, Uganda; Departments of Medicine (Smith) and Psychiatry and Behavioral Sciences (Smith), Duke University Medical Center, Durham, North Carolina; Department of Psychology (Wamala), Center for Victims of Torture; Department of Mental Health, Faculty of Medicine (Okello), Gulu University, Gulu; The AIDS Support Organization (TASO) (Birungi, Etukoit), Kampala, Uganda; Department of Mental Health, Bloomberg's School of Public Health (Mojtabai), Johns Hopkins University, Baltimore, Maryland; Department of Epidemiology, Pittsburgh Graduate School of Public Health (Nachega), University of Pittsburgh, Pittsburgh, Pennsylvania; Stellenbosch Center for Infectious Disease, Department of Medicine (Nachega), Stellenbosch University, Stellenbosch, South Africa; Department of International Health, Bloomberg's School of Public Health (Nachega), Johns Hopkins University, Baltimore, Maryland; MTEK Sciences Inc (Harari), Vancouver, British Columbia; and Department of Clinical Epidemiology and Biostatistics (Mills), McMaster University, Hamilton, Ontario, Canada.

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