Diabetes Clinical Trial
Official title:
The Effects of Computerized Cognitive Training on Diabetic Elderly, Who Are at High Risk for Dementia
The current study examines the efficiency of a home-based computerized cognitive training (CT) intervention targeting older adults with diabetes.The primary aim of the study is to evaluate the effects of CCT on cognitive and disease management in non-demented older diabetes adults. Investigators will also evaluate the effect of the intervention on a range of secondary outcomes, including mood, caregiver burden, self-efficacy, and for a small sub-sample, on brain activity as reflected in changes in task-related blood-flow on fMRI.
Evidence suggests a link between diabetes-related processes and increased risk of cognitive
decline and dementia in older adults. Optimal disease self-management may be key in the
prevention of cognitive decline among older diabetic patients, but this may be compromised
due to sub-clinical cognitive impairment.
In the current study, 120 community-dwelling, non-demented participants aged 65 and over,
with a diagnosis of Type 2 diabetes will be randomly assigned either to an 8-week, home-based
individually-tailored CCT program with adaptive difficulty level, and regular performance
feedback, or to an 8-week, home-based active control (AC) condition, involving training on a
generic CCT program with fixed difficulty level and without performance feedback. Both
intervention groups also include a range of theory-informed behavior change techniques
(BCTs), including self-efficacy management, self-monitoring and goal-setting in order to
enhance treatment fidelity, and to maximize treatment compliance and adherence. In both
groups, participants train approx. 30 min. per day, 3 times per-week for 8-weeks.
Participants undergo a comprehensive evaluation of all outcomes at baseline, immediately
after the intervention, and at a 6-month follow-up, with 1-week booster training completed 3
months from completion of the intervention.
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