The Active Brains Digital Intervention to Reduce Cognitive Decline in Older Adults: Protocol for a Feasibility Randomized Controlled Trial

Author:

Smith Kirsten AilsaORCID,Bradbury KatherineORCID,Essery RosieORCID,Pollet SebastienORCID,Mowbray FionaORCID,Slodkowska-Barabasz JoannaORCID,Denison-Day JamesORCID,Hayter VictoriaORCID,Kelly JoORCID,Somerville JaneORCID,Zhang JinORCID,Grey ElisabethORCID,Western MaxORCID,Ferrey Anne EORCID,Krusche AdeleORCID,Stuart BethORCID,Mutrie NanetteORCID,Robinson SianORCID,Yao Guiqing LilyORCID,Griffiths GarethORCID,Robinson LouiseORCID,Rossor MartinORCID,Gallacher JohnORCID,Griffin SimonORCID,Kendrick TonyORCID,Rathod ShanayaORCID,Gudgin BernardORCID,Phillips RosemaryORCID,Stokes TomORCID,Niven JohnORCID,Little PaulORCID,Yardley LucyORCID

Abstract

Background Increasing physical activity, improving diet, and performing brain training exercises are associated with reduced cognitive decline in older adults. Objective In this paper, we describe a feasibility trial of the Active Brains intervention, a web-based digital intervention developed to support older adults to make these 3 healthy behavior changes associated with improved cognitive health. The Active Brains trial is a randomized feasibility trial that will test how accessible, acceptable, and feasible the Active Brains intervention is and the effectiveness of the study procedures that we intend to use in the larger, main trial. Methods In the randomized controlled trial (RCT), we use a parallel design. We will be conducting the intervention with 2 populations recruited through GP practices (family practices) in England from 2018 to 2019: older adults with signs of cognitive decline and older adults without any cognitive decline. Trial participants were randomly allocated to 1 of 3 study groups: usual care, the Active Brains intervention, or the Active Brains website plus brief support from a trained coach (over the phone or by email). The main outcomes are performance on cognitive tasks, quality of life (using EuroQol-5D 5 level), Instrumental Activities of Daily Living, and diagnoses of dementia. Secondary outcomes (including depression, enablement, and health care costs) and process measures (including qualitative interviews with participants and supporters) will also be collected. The trial has been approved by the National Health Service Research Ethics Committee (reference 17/SC/0463). Results Results will be published in peer-reviewed journals, presented at conferences, and shared at public engagement events. Data collection was completed in May 2020, and the results will be reported in 2021. Conclusions The findings of this study will help us to identify and make important changes to the website, the support received, or the study procedures before we progress to our main randomized phase III trial. Trial Registration International Standard Randomized Controlled Trial Number 23758980; http://www.isrctn.com/ISRCTN23758980 International Registered Report Identifier (IRRID) DERR1-10.2196/18929

Publisher

JMIR Publications Inc.

Subject

General Medicine

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