Abstract

AbstractBackgroundGOIZ ZAINDU (“caring early” in Basque) is a pilot study to adapt FINGER methodology to the Basque Population and evaluate feasibility and adherence to a FINGER‐like multimodal intervention program. Additional exploratory aims included assessment of efficacy on cognition and collection of necessary data to design a large efficacy trial.MethodGOIZ ZAINDU is a one year, randomized, controlled trial of a multimodal intervention in persons aged 60+ with increased CAIDE score (≥ 6), no dementia, and below‐than‐expected performance in at least one of three cognitive screening tests. Participants were recruited from a previous program on early diagnosis and risk awareness (GOIZ‐ALZHEIMER). Randomization to a Multimodal intervention (MI) or to Regular Health Advice (RHA) was stratified by cognitive status (MCI/normal) and age (>/≤ 75). MI included cardiovascular risk factors control, nutritional counseling, physical activity and cognitive training. Primary outcome was adherence to intervention program. Cognitive outcomes included Neuropsychological Test Battery z scores change. Analyses were carried out by intention to treat.Result125 participants were recruited (mean age: 75.64 (6.46); 58% women). MI (n=61) and RHA (n=64) groups were balanced in demographics and cognition (Table 1). 52 (85%) participants from RHA and 56 (88%) from MI group completed the study. 55% of participants had attended all intervention activities; 70% attended more than half of cognitive sessions; and 55% attended more than half of cardiovascular, nutritional and physical activity program sessions Risk of cognitive decline was higher in RHA group compared with MI in executive Function (EF)(p=.019) and Processing Speed (PS) scores (p=.026) (Table 2). 32 (64%) participants In the RHA and 22 (40%) in the MI group declined in EF; 30 persons (61%) in the RHA and 22 (39%) in the MI declined in PS,ConclusionThe GOIZ‐ZAINDU study has proved that the FINGER methodology is adaptable and feasible in a different socio‐cultural environment. Exploratory efficacy results show lower risk of decline in EF and PS. These results support the design of a large‐scale efficacy FINGER‐like trial in Southern Europe, the GO‐ON study.

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