Aged
Conditions
Interventions
A baseline assessment will be performed and subsequently individuals will be randomly distributed to receive 100mg of modafinil or placebo. One of the groups will start with modafinil (n=24), while th
D02.455.426.559.389.115.550
Sponsors
Faculdade de Medicina de Ribeirão Preto
Universidade Federal de São Carlos
Eligibility
Age
60 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals 60 years of age or older; Be available to return for revaluations and have a telephone to contact
Exclusion criteria
Exclusion criteria: Presence of uncontrolled moderate to severe hypertension; Presence of cardiac arrhythmias, according to self-report; Hearing Loss; Use of Benzodiazepine; Use of cholinesterase inhibitors; medical diagnosis of Dementia, according to self-report
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to verify the improvement in cognition and learning in the elderly after acute administration of modafinil | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Countries
Brazil
Contacts
Public ContactAna Julia Bomfim
Universidade Federal de São Carlos
Outcome results
None listed