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Article: Protocol for a mixed-methods randomised controlled trial evaluating the psychosocial effects of an expressive arts-based intervention on adults with age-related macular degeneration

TitleProtocol for a mixed-methods randomised controlled trial evaluating the psychosocial effects of an expressive arts-based intervention on adults with age-related macular degeneration
Authors
KeywordsGERIATRIC MEDICINE
OPHTHALMOLOGY
Randomized Controlled Trial
Issue Date20-Dec-2024
PublisherBMJ Publishing Group
Citation
BMJ Open, 2024, v. 14, n. 12 How to Cite?
AbstractIntroduction Age-related macular degeneration (AMD) is a prevalent eye disease among middle-aged and older adults. AMD leaves the patient with irreversible deteriorating vision, which profoundly impacts their daily lives and psychosocial well-being. Given the limited studies addressing the psychosocial needs of adults with AMD and, in particular, using an expressive arts-based intervention (EXABI) as an intervention, this study aims to investigate the effectiveness of such an intervention in enhancing the psychosocial well-being of adults with AMD. Methods and analysis This study will employ a mixed-methods randomised controlled trial design. One hundred fifty-four participants with AMD will be recruited and randomised into either the EXABI or treatment-as-usual waitlist control group. Participants will respond to a battery of measurements regarding their psychosocial condition at four time points: baseline (T 0), 2 months after baseline (postintervention, T 1), 5 months after baseline (T 2) and 8 months after baseline (T 3). A subgroup of participants will also share their experiences through in-depth interviews at T 1 and T 3 to help further understand the mechanism and effect of the intervention. Quantitative data will be analysed by mixed-effects models and path analysis, whereas qualitative data will be analysed by adopting the thematic analysis approach. The two sets of data will be integrated to provide a comprehensive view of the effectiveness and mechanisms of the intervention. Ethics and dissemination This study has obtained ethical approval from the Human Research Ethics Committee of the University of Hong Kong (Ref. no.: EA210606). All research procedures will be conducted upon receiving signed written consent forms from participants. The findings of the study will also be presented at international conferences and published in peer-reviewed academic journals.
Persistent Identifierhttp://hdl.handle.net/10722/354590

 

DC FieldValueLanguage
dc.contributor.authorHo, Rainbow Tin Hung-
dc.contributor.authorCheong, Allen Ming Yan-
dc.contributor.authorWan, Adrian Ho Yin-
dc.contributor.authorLo, Temmy Lee Ting-
dc.contributor.authorFong, Ted Chun Tat-
dc.contributor.authorChan, Caitlin Kar Pui-
dc.contributor.authorLi, Qing-
dc.contributor.authorChan, Wai Chi-
dc.date.accessioned2025-02-23T00:35:11Z-
dc.date.available2025-02-23T00:35:11Z-
dc.date.issued2024-12-20-
dc.identifier.citationBMJ Open, 2024, v. 14, n. 12-
dc.identifier.urihttp://hdl.handle.net/10722/354590-
dc.description.abstractIntroduction Age-related macular degeneration (AMD) is a prevalent eye disease among middle-aged and older adults. AMD leaves the patient with irreversible deteriorating vision, which profoundly impacts their daily lives and psychosocial well-being. Given the limited studies addressing the psychosocial needs of adults with AMD and, in particular, using an expressive arts-based intervention (EXABI) as an intervention, this study aims to investigate the effectiveness of such an intervention in enhancing the psychosocial well-being of adults with AMD. Methods and analysis This study will employ a mixed-methods randomised controlled trial design. One hundred fifty-four participants with AMD will be recruited and randomised into either the EXABI or treatment-as-usual waitlist control group. Participants will respond to a battery of measurements regarding their psychosocial condition at four time points: baseline (T 0), 2 months after baseline (postintervention, T 1), 5 months after baseline (T 2) and 8 months after baseline (T 3). A subgroup of participants will also share their experiences through in-depth interviews at T 1 and T 3 to help further understand the mechanism and effect of the intervention. Quantitative data will be analysed by mixed-effects models and path analysis, whereas qualitative data will be analysed by adopting the thematic analysis approach. The two sets of data will be integrated to provide a comprehensive view of the effectiveness and mechanisms of the intervention. Ethics and dissemination This study has obtained ethical approval from the Human Research Ethics Committee of the University of Hong Kong (Ref. no.: EA210606). All research procedures will be conducted upon receiving signed written consent forms from participants. The findings of the study will also be presented at international conferences and published in peer-reviewed academic journals.-
dc.languageeng-
dc.publisherBMJ Publishing Group-
dc.relation.ispartofBMJ Open-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectGERIATRIC MEDICINE-
dc.subjectOPHTHALMOLOGY-
dc.subjectRandomized Controlled Trial-
dc.titleProtocol for a mixed-methods randomised controlled trial evaluating the psychosocial effects of an expressive arts-based intervention on adults with age-related macular degeneration-
dc.typeArticle-
dc.identifier.doi10.1136/bmjopen-2024-088311-
dc.identifier.scopuseid_2-s2.0-85214438416-
dc.identifier.volume14-
dc.identifier.issue12-
dc.identifier.eissn2044-6055-
dc.identifier.issnl2044-6055-

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