Status:
UNKNOWN
GAmified HOme-based COgnitive-Nutritional Training Feasibility Study
Lead Sponsor:
The Hong Kong Polytechnic University
Collaborating Sponsors:
Tung Wah College
Mindvivid
Conditions:
Cognitive Frailty
Protective Diet Adherence
Eligibility:
All Genders
60+ years
Phase:
NA
Brief Summary
Background: Cognitive frailty is an at-risk state of dementia that it can be reversed by manipulating the lifestyle factors, such as cognitive activity and nutrition/dietary pattern. Their protective ...
Detailed Description
Methods: This study employs a pilot randomized controlled trial design. Recruitment will be conducted in elderly community centres. Participants who are aged ≥ 60 years, community-dwelling, and having...
Eligibility Criteria
Inclusion
- Age ≥ 60 years,
- Community-dwelling, as defined by living at home without staying in long-term care facilities (e.g., nursing home) in the last 12 months as reported by the participants,
- Cognitive frailty, as defined by co-existence of mild cognitive impairment and physical frailty,7
- Mild cognitive impairment, measured by Montreal Cognitive Assessment (MoCA) score ≤ 25 and Clinical Dementia Rating (CDR) score = 0.5,35,36 and
- Frailty status from pre-frail to frail, measured by Fried Frailty Phenotype score ≥ 1.37
- Poor Mediterranean diet adherence, measured by MDS score \< 30.5 (i.e., the mean MDS of community-dwelling older people reported in a local study),20 and
- Functionally independent on food preparation, as defined by Lawton Instrumental Activity of Daily Living score ≥ 15/18 with the sub-score on Meal Preparation = 2/2.38,39
Exclusion
- Diagnosed dementia, according to subjects' medical record, or
- Probable dementia, as defined by MoCA ≤ 18,35,36
- Low vision (at least one eye with visual acuity \< 20/60) or without corrective lens, because all training are visual-based and blurred vision negatively affects cognitive performance in cognitive training and assessment.40
Key Trial Info
Start Date :
May 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 14 2022
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05207930
Start Date
May 1 2022
End Date
May 14 2022
Last Update
January 26 2022
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