In 2020, the global prevalence of dementia exceeded 55 million individuals
Previous research has shown that a task may be able to predict the likelihood of developing dementia from MCI
My PhD aims to explore a similar task as there were limitations of Nitka et al’s (2020) task for example the images used were all easy to verbally distinguish (e.g. violin and hand), which means it could be testing verbal memory as well as recognition memory. Therefore, one of my studies will explore a similar task to this with healthy individuals however the 6 images within each trial will be more similar (e.g. in one trial all of the 6 images will be of the moon). Hence, this study will assess whether self- and retrieval-generated priming can be more accurately measured through relative recency and object-in-place. This approach offers a purer gauge of recognition memory compared to prior methods, particularly considering the increased difficulty in verbally discriminating the images.
The potential following study could explore whether this computerised task could predict cognitive decline in individuals with MCIs. The use of relative recency and object-in-place may detect a selective deficit. This would mean that this task would presumably be more sensitive to a decline in cognitive performance compared to previous studies because a single affected form of priming could be compensated by the other form. In order to conduct this research, I will administer the ACE-3 with the task and again one year later to measure their cognitive function and decline.
Additionally, this research may explore the eye movement data from the eye trackers to predict cognitive decline in individuals with MCI. As previous research found individuals with Alzheimer’s disease have different eye movement data compared to healthy controls
If the results are significant, this task could be utilised within GP settings to help medical staff and the patient know who is at risk of cognitive decline in the next year. Earlier detection would allow timely interventions and enrolment into clinical trials when treatments are most effective at slowing progression.
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