The APPLE Tree programme: Active Prevention in People at risk of dementia through Lifestyle, bEhaviour change and Technology to build REsiliEnce—randomised controlled trial

Poppe, M., Duffy, L., Marchant, N. L., Barber, J. A., Hunter, R., Bass, N., Minihane, A. M. ORCID: https://orcid.org/0000-0001-9042-4226, Walters, K., Higgs, P., Rapaport, P., Lang, I. A., Morgan-Trimmer, S., Huntley, J., Walker, Z., Brodaty, H., Kales, H. C., Ritchie, K., Burton, A., Wenborn, J., Betz, A. and Cooper, C. (2022) The APPLE Tree programme: Active Prevention in People at risk of dementia through Lifestyle, bEhaviour change and Technology to build REsiliEnce—randomised controlled trial. Trials, 23. ISSN 1745-6215

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Abstract

Background: Large-scale trials of multidomain interventions show that modifying lifestyle and psychological risk factors can slow cognitive decline. We aim to determine if a lower intensity, personally tailored secondary dementia prevention programme for older people with subjective or mild objective memory decline, informed by behaviour change theory, reduces cognitive decline over 2 years. Methods: A multi-site, single-blind randomised controlled trial recruiting 704 older adults at high dementia risk due to mild cognitive impairment (MCI) or subjective cognitive decline (SCD). Participants are randomised using 1:1 allocation ratio to the APPLE Tree intervention versus control arm (dementia prevention information), stratified by site. The intervention explores and implements strategies to promote healthy lifestyle, increase pleasurable activities and social connections and improve long-term condition self-management. Two facilitators trained and supervised by a clinical psychologist deliver ten, 1-h group video call sessions over 6 months (approximately every fortnight), video-call 'tea breaks' (less structured, facilitated social sessions) in intervening weeks and individual goal-setting phone calls every 2 weeks. From 6 to 12 months, participants meet monthly for 'tea breaks', with those not attending receiving monthly goal-setting phone calls. Participants receive a food delivery, pedometer and website access to cognitive training and information about lifestyle modification. Follow-ups for all outcome measures are at 12 and 24 months. The primary outcome is cognition (Neuropsychological Test Battery (NTB) score) at 24 months. Secondary outcomes are quality of life, cost per quality-adjusted life year (QALY) and wellbeing and lifestyle factors the intervention targets (diet, vascular risk, body weight, activity, sleep, anxiety, depression, social networks and loneliness, alcohol intake and smoking). Participants from purposively selected sites participate in qualitative process evaluation interviews, which will be analysed using thematic analytic methods. Discussion: If effective, the intervention design, involving remote delivery and non-clinical facilitators, would facilitate intervention roll-out to older people with memory concerns. Trial registration: ISRCTN17325135 . Registration date 27 November 2019.

Item Type: Article
Additional Information: Funding Information: The study is funded by an Economic and Social Research Council/National Institute for Health Research programme grant (ES/S010408/1). The funders have not been involved in the design of the study, collection, analysis and interpretation of data and in writing the manuscript. IL is supported by the National Institute for Health Research Applied Research Collaboration South West Peninsula. The views expressed in this publication are those of the author(s) and not necessarily those of the National Institute for Health Research or the Department of Health and Social Care.
Uncontrolled Keywords: randomised controlled trial,medicine (miscellaneous),pharmacology (medical),sdg 3 - good health and well-being ,/dk/atira/pure/subjectarea/asjc/2700/2701
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
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Depositing User: LivePure Connector
Date Deposited: 05 Oct 2022 16:30
Last Modified: 25 Oct 2022 12:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/88868
DOI: 10.1186/s13063-022-06557-6

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