Finding studies
Finding studies
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Lead
Assistance Publique - Hôpitaux de Paris
It is a monocentric, controlled, randomized, parallel-group, single-blind clinical trial. For each of the two forms of Alzheimer's Disease (young or late), it compares two groups of patients: a group benefiting from a tactile tablet semantic stimulation (tablet group) and a control group All patients benefit from a clinical evaluation and a language assessment at M0, M3 and M6. The analyzes will be conducted in intention to treat. The main criterion is the 3-month variation of the Lexis 3 subtests scores. The two groups will be compared by the Student test. The number of subjects required is based on the following assumptions: a 10% increase over three months of the Lexis subtests scores in the tablet group and a stability of the scores in the control group. The standard deviation of the variation is assumed to be identical in both groups and equal to 13% at the most. Three scores being compared, tests will be conducted at the 1.67% threshold (Bonferroni correction) to ensure a 5% overall risk of first species. The inclusion of 36 patients in each of the two treatment groups will give 80% power to the study.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
