Healthy Clinical Trial
Official title:
Donepezil Effect on Visual Attention and Perceptual Training in Healthy Young Adults
| Verified date | August 2015 |
| Source | Université de Montréal |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The present proposal investigates the role of the cholinergic system (the neurotransmitter
acetylcholine) in improving vision and visual attention. Vision results from a complex
processing of particular stimuli of the visual field. Attention enhances and prolongs the
neural representations of visual input in the visual cortex. It has recently been shown that
attention in the visual cortex depends on cholinergic mechanisms. The action of
acetylcholine in the visual cortex consists in enhancement of the responsiveness to
thalamocortical inputs, depression of local neuronal connections or extrastriate feedback
projections and induction of gamma synchronisation. The investigators hypothesize that these
effects are associated with long-term changes in functional connectivity in the visual
cortex, visual attention and visual learning (improvement of the visual capacities).
In the present proposal, the investigators will test whether the administration of donepezil
(Aricept, 5mg), a drug that increases the level of acetylcholine in the brain, will enhances
the perceptual-cognitive abilities of young adult subjects. Perceptual-cognitive performance
will be assessed in a multiple object tracking (MOT) task in a 3D automatic virtual
environment. MOT is a task where observers are asked to maintain attentional focus on a
limited number of preselected subgroup of elements in a dynamic scene. Multifocal
attentional mechanisms are necessary to process the information. The task will be tested
five time at one week interval to test whether donepezil and training improved the task
performance of the subject, i.e. lead to perceptual learning. This study could help
establish an intervention procedure to improve visual performance of subjects that need it.
| Status | Completed |
| Enrollment | 20 |
| Est. completion date | August 2015 |
| Est. primary completion date | August 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 20 Years to 35 Years |
| Eligibility |
Inclusion Criteria: - good general health - 17 < body mass index < 25 - visual acuity 6/6 - visual stereoscopy > 50 - standard visual field Exclusion Criteria: - pregnancy or breast feeding - use of any drug or St John's wort - smoking - asthma - pulmonary obstruction - cardiovascular impairment - attention troubles - ocular diseases - epilepsy - lactose intolerance - absorption of grapefruit juice |
| Country | Name | City | State |
|---|---|---|---|
| Canada | School of optometry / Université de Montréal | Montréal | Quebec |
| Lead Sponsor | Collaborator |
|---|---|
| Université de Montréal |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Measure of the speed threshold, baseline | The speed of the moving spheres is increased across trials until the subject is not able anymore to track and identify the indexed spheres (speed threshold). In this baseline task, the subject will not take Donepezil or placebo | week 0 | |
| Primary | Change from baseline of the speed threshold at 1 week | The speed of the moving spheres is increased across trials. The maximal speed for which the subject is able to track and identify the indexed spheres is the speed threshold. At this time point, the effect of Donepezil (5 mg, single dose) or placebo administration on the perceptual-cognitive performance will be assessed. | week 1 | |
| Primary | Change from baseline of the speed threshold at 2 weeks | The speed of the moving spheres is increased across trials. The maximal speed for which the subject is able to track and identify the indexed spheres is the speed threshold. At this time point, the effect of Donepezil (5 mg, single dose) or placebo administration on the perceptual-cognitive performance will be assessed. | week 2 | |
| Primary | Change from baseline of the speed threshold at 3 weeks | The speed of the moving spheres is increased across trials. The maximal speed for which the subject is able to track and identify the indexed spheres is the speed threshold. At this time point, the effect of Donepezil (5 mg, single dose) or placebo administration on the perceptual-cognitive performance will be assessed. | week 3 | |
| Primary | Change from baseline of the speed threshold at 4 weeks | The speed of the moving spheres is increased across trials. The maximal speed for which the subject is able to track and identify the indexed spheres is the speed threshold. At this time point, the effect of Donepezil (5 mg, single dose) or placebo administration on the perceptual-cognitive performance will be assessed. | week 4 |
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