학술논문

The APPLE Tree programme: Active Prevention in People at risk of dementia through Lifestyle, bEhaviour change and Technology to build REsiliEnce—randomised controlled trial
Document Type
article
Source
Trials. 23(1)
Subject
Health Services and Systems
Health Sciences
Clinical Trials and Supportive Activities
Aging
Acquired Cognitive Impairment
Brain Disorders
Alzheimer's Disease
Dementia
Neurosciences
Mental Health
Behavioral and Social Science
Neurodegenerative
Prevention
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Clinical Research
Nutrition
Evaluation of treatments and therapeutic interventions
Prevention of disease and conditions
and promotion of well-being
7.1 Individual care needs
3.1 Primary prevention interventions to modify behaviours or promote wellbeing
6.6 Psychological and behavioural
Management of diseases and conditions
Mental health
Neurological
Cardiovascular
Good Health and Well Being
Aged
Cost-Benefit Analysis
Humans
Life Style
Malus
Quality of Life
Single-Blind Method
Tea
Technology
Randomised controlled trial
Cardiorespiratory Medicine and Haematology
Clinical Sciences
Cardiovascular System & Hematology
General & Internal Medicine
Clinical sciences
Epidemiology
Health services and systems
Language
Abstract
BackgroundLarge-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.MethodsA 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.DiscussionIf effective, the intervention design, involving remote delivery and non-clinical facilitators, would facilitate intervention roll-out to older people with memory concerns.Trial registrationISRCTN17325135 . Registration date 27 November 2019.