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Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program
BACKGROUND: Stroke patients with aphasia and their caregivers have higher incidence of depression than those without aphasia. AIMS: The objective of the study is to determine whether a tailored intervention program (Action Success Knowledge; ASK) led to better mood and quality of life (QoL) outcomes...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507993/ https://www.ncbi.nlm.nih.gov/pubmed/37154589 http://dx.doi.org/10.1177/17474930231176718 |
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author | Ryan, Brooke Kneebone, Ian Rose, Miranda L. Togher, Leanne Power, Emma Hoffmann, Tammy Khan, Asaduzzaman Simmons-Mackie, Nina Carragher, Marcella Worrall, Linda |
author_facet | Ryan, Brooke Kneebone, Ian Rose, Miranda L. Togher, Leanne Power, Emma Hoffmann, Tammy Khan, Asaduzzaman Simmons-Mackie, Nina Carragher, Marcella Worrall, Linda |
author_sort | Ryan, Brooke |
collection | PubMed |
description | BACKGROUND: Stroke patients with aphasia and their caregivers have higher incidence of depression than those without aphasia. AIMS: The objective of the study is to determine whether a tailored intervention program (Action Success Knowledge; ASK) led to better mood and quality of life (QoL) outcomes than an attention control with a 12-month end point at cluster and individual participant level. METHODS: A multi-site, pragmatic, two-level single-blind cluster randomized controlled trial compared ASK to an attention control (secondary stroke prevention program). Ten metropolitan and 10 non-metropolitan health regions were randomized. People with aphasia and their family members were recruited within 6 months post-stroke who scored ⩽12 on the Stroke Aphasic Depression Questionnaire Hospital Version–10 at screening. Each arm received manualized intervention over 6–8 weeks followed by monthly telephone calls. Blinded assessments of QoL and depression were taken at 12 months post-onset. RESULTS: Twenty clusters (health regions) were randomized. Trained speech pathologists screened 1744 people with aphasia and 373 participants consented to intervention (n = 231 people with aphasia and 142 family members). The attrition rate after consent was 26% with 86 and 85 participants with aphasia in the ASK arm and attention control arm, respectively, receiving intervention. Of those 171 who did receive treatment, only 41 met the prescribed minimum dose. Multilevel mixed effects modeling under the intention-to-treat protocol showed a significant difference on the Stroke and Aphasia Depression Questionnaire–21 (SADQ-21, N = 122, 17 clusters) in favor of the attention control (β = –2.74, 95% confidence interval (CI) = –4.76 to –0.73, p = 0.008). Individual data analysis using a minimal detectable change score for the SADQ-21 showed the difference was not meaningful. CONCLUSION: ASK showed no benefit over attention control in improving mood and preventing depression in people with aphasia or their family members. |
format | Online Article Text |
id | pubmed-10507993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-105079932023-09-20 Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program Ryan, Brooke Kneebone, Ian Rose, Miranda L. Togher, Leanne Power, Emma Hoffmann, Tammy Khan, Asaduzzaman Simmons-Mackie, Nina Carragher, Marcella Worrall, Linda Int J Stroke Research BACKGROUND: Stroke patients with aphasia and their caregivers have higher incidence of depression than those without aphasia. AIMS: The objective of the study is to determine whether a tailored intervention program (Action Success Knowledge; ASK) led to better mood and quality of life (QoL) outcomes than an attention control with a 12-month end point at cluster and individual participant level. METHODS: A multi-site, pragmatic, two-level single-blind cluster randomized controlled trial compared ASK to an attention control (secondary stroke prevention program). Ten metropolitan and 10 non-metropolitan health regions were randomized. People with aphasia and their family members were recruited within 6 months post-stroke who scored ⩽12 on the Stroke Aphasic Depression Questionnaire Hospital Version–10 at screening. Each arm received manualized intervention over 6–8 weeks followed by monthly telephone calls. Blinded assessments of QoL and depression were taken at 12 months post-onset. RESULTS: Twenty clusters (health regions) were randomized. Trained speech pathologists screened 1744 people with aphasia and 373 participants consented to intervention (n = 231 people with aphasia and 142 family members). The attrition rate after consent was 26% with 86 and 85 participants with aphasia in the ASK arm and attention control arm, respectively, receiving intervention. Of those 171 who did receive treatment, only 41 met the prescribed minimum dose. Multilevel mixed effects modeling under the intention-to-treat protocol showed a significant difference on the Stroke and Aphasia Depression Questionnaire–21 (SADQ-21, N = 122, 17 clusters) in favor of the attention control (β = –2.74, 95% confidence interval (CI) = –4.76 to –0.73, p = 0.008). Individual data analysis using a minimal detectable change score for the SADQ-21 showed the difference was not meaningful. CONCLUSION: ASK showed no benefit over attention control in improving mood and preventing depression in people with aphasia or their family members. SAGE Publications 2023-06-05 2023-10 /pmc/articles/PMC10507993/ /pubmed/37154589 http://dx.doi.org/10.1177/17474930231176718 Text en © 2023 World Stroke Organization https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Ryan, Brooke Kneebone, Ian Rose, Miranda L. Togher, Leanne Power, Emma Hoffmann, Tammy Khan, Asaduzzaman Simmons-Mackie, Nina Carragher, Marcella Worrall, Linda Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title | Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title_full | Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title_fullStr | Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title_full_unstemmed | Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title_short | Preventing depression in aphasia: A cluster randomized control trial of the Aphasia Action Success Knowledge (ASK) program |
title_sort | preventing depression in aphasia: a cluster randomized control trial of the aphasia action success knowledge (ask) program |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507993/ https://www.ncbi.nlm.nih.gov/pubmed/37154589 http://dx.doi.org/10.1177/17474930231176718 |
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