The effect of co-morbid anxiety on remission from depression for people participating in a randomised controlled trial of the Friendship Bench intervention in Zimbabwe.

Anxiety Global health Low and middle income countries Mental health Persistent Depression Primary care

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jun 2020
Historique:
entrez: 9 7 2020
pubmed: 9 7 2020
medline: 9 7 2020
Statut: epublish

Résumé

There is a lack of data from low- and middle-income countries on whether anxiety independently predicts a more chronic course for depression. We undertook secondary data analysis of a cluster randomised controlled trial in Zimbabwe which had tested the effectiveness of the Friendship Bench intervention for common mental disorders compared to enhanced usual care. Inclusion for the current study was participants from the trial who had probable major depression at baseline, defined as scoring => 11 on the locally validated Patient Health Questionnaire (PHQ9). This emerged to be 354 of the original 573 (61.78%) of the original trial sample. Anxiety was measured using the locally validated cut-point on the Generalised Anxiety Disorder scale (GAD-7). Persistent depression was defined as scoring => 11 on the PHQ-9 at six-months follow-up. Analysis in Stata 15 used random-effects logistic regression to adjust for clustering by clinic. Of the 354 participants who were eligible for treatment, 329 (92·9%) completed 6-month follow-up assessment. 37% of the trial sample had persistent depression at 6-months follow-up; 59% in the control arm and 17% in the intervention arm. Co-morbid anxiety present at trial baseline was independently associated with persistent depression after adjusting for age, gender and baseline depression severity (adjusted OR = 2·83, 95% CI 1·32-6·07). There was no evidence of effect modification by trial arm. Baseline depression severity also predicted persistent depression.

Sections du résumé

BACKGROUND BACKGROUND
There is a lack of data from low- and middle-income countries on whether anxiety independently predicts a more chronic course for depression.
METHODS METHODS
We undertook secondary data analysis of a cluster randomised controlled trial in Zimbabwe which had tested the effectiveness of the Friendship Bench intervention for common mental disorders compared to enhanced usual care. Inclusion for the current study was participants from the trial who had probable major depression at baseline, defined as scoring => 11 on the locally validated Patient Health Questionnaire (PHQ9). This emerged to be 354 of the original 573 (61.78%) of the original trial sample. Anxiety was measured using the locally validated cut-point on the Generalised Anxiety Disorder scale (GAD-7). Persistent depression was defined as scoring => 11 on the PHQ-9 at six-months follow-up. Analysis in Stata 15 used random-effects logistic regression to adjust for clustering by clinic.
OUTCOMES RESULTS
Of the 354 participants who were eligible for treatment, 329 (92·9%) completed 6-month follow-up assessment. 37% of the trial sample had persistent depression at 6-months follow-up; 59% in the control arm and 17% in the intervention arm. Co-morbid anxiety present at trial baseline was independently associated with persistent depression after adjusting for age, gender and baseline depression severity (adjusted OR = 2·83, 95% CI 1·32-6·07). There was no evidence of effect modification by trial arm. Baseline depression severity also predicted persistent depression.

Identifiants

pubmed: 32637890
doi: 10.1016/j.eclinm.2020.100333
pii: S2589-5370(20)30077-8
pii: 100333
pmc: PMC7329733
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100333

Informations de copyright

© 2020 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

We declare no conflicts of interests.

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Auteurs

Melanie Amna Abas (MA)

King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Centre for Anxiety Disorders and Trauma, South London and Maudsley NHS Foundation Trust, London, UK.

Helen Anne Weiss (HA)

MRC Tropical Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.

Victoria Simms (V)

MRC Tropical Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.

Ruth Verhey (R)

Research Support Centre, University of Zimbabwe, Harare, Zimbabwe.

Simbarashe Rusakaniko (S)

Zimbabwe AIDS Prevention Project-University of Zimbabwe Department of Community Medicine, Harare, Zimbabwe.

Ricardo Araya (R)

King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.

Dixon Chibanda (D)

Research Support Centre, University of Zimbabwe, Harare, Zimbabwe.
Centre for Global Mental Health, London School of Hygiene and Tropical Medicine, London, UK.

Classifications MeSH