Reducing Cognitive Impairment in Older Adults: Development Phase

  • Research type

    Research Study

  • Full title

    REducing and preventing COgnitive impairment iN older age groups (the RECON Programme)Development Phase

  • IRAS ID

    228584

  • Contact name

    Paul Little

  • Contact email

    P.Little@soton.ac.uk

  • Sponsor organisation

    University of Southampton

  • Duration of Study in the UK

    1 years, 2 months, 26 days

  • Research summary

    The prevalence of dementia is between 5 and 7% amongst over 65 year-olds in the UK. Cognitive impairment in the absence of dementia is even more common, and approximately 10% of cases convert to dementia each year. However, there is substantial evidence that healthy behaviours, including physical activity, cognitive training tasks and healthy eating have positive effects on cognitive function. Despite this, such face-to-face interventions can be costly. This research is part of a programme of study to determine whether internet-based interventions for older adults are an effective and cost-effective means of facilitating practice of these healthy behaviours to: reduce cognitive decline amongst those with pre-existing cognitive impairment (workstream one: WS1); and to maintain cognitive functioning in healthy older adults (workstream two: WS2). The qualitative research outlined here aims to ensure that the interventions are developed in line with the needs and preferences of target users to ensure that they are acceptable and accessible. Two qualitative studies will be conducted, including 60-90 older adults both with and without cognitive impairment. After giving informed consent participants will be asked to share their thoughts and feelings about early versions of the intervention and any issues they raise for facilitating healthy behaviour change to benefit brain health:
    Study 1: face-to-face 'think aloud' interviews where patients give 'live' feedback as they view and use the website.
    Study 2: retrospective telephone or face-to-face interviews with patients giving feedback on the website after trying it for one to three weeks in their own home.
    This phase will also involve reviewing existing theoretical and empirical literature to systematically inform intervention content, structure, and functionality. Once fully developed and modified in response to feedback from the current studies the interventions will be tested in feasibility trials and large scale Randomised Controlled Trials (RCTs) (detailed in later applications).

  • REC name

    South Central - Hampshire B Research Ethics Committee

  • REC reference

    17/SC/0463

  • Date of REC Opinion

    28 Sep 2017

  • REC opinion

    Further Information Favourable Opinion