Eye diseases
Conditions
Interventions
Group 1: 20 visually impaired people will perform the virtual task of coincident timing on a computer following the intervention protocol.
Group 2: 20 people without visual impairment will perform th
Phase 2 - Rest (5 minutes)
Phase 3 - 5 attempts (refers to the phase for analyzing learning retention)
Phase 4 - 5 attempts (refers to the ability to transfer the activity to a faster mode)
Phase 5 - Rest (24 hours - the participant leaves and follows his routine)
Phase 6 - 5 attempts (refers to the phase for analyzing long-term learning retention
Phase 7 - 5 attempts (refers to the long-term ability to transfer the activity to a faster mode).
L01.224.160.875
Sponsors
Universidade de Franca
Universidade de Franca
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The criteria for participation in the research are: agreement to participate in the research; be over 18 years old; sign the Informed Consent Form; have visual disorder diagnosis and understand the virtual task. For the seers group follows the same criteria above without the diagnosis of visual disorder.
Exclusion criteria
Exclusion criteria: The criteria for non-inclusion in the study include dropout during the protocol and functional and cognitive disabilities that prevent the accomplishment of the virtual task.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Primary
| Measure | Time frame |
|---|---|
| Different results of coincident time analysis are expected to be found between the three groups.;It is expected that the group of people with visual impairment will have rapid learning skills in the practical phase.;It is expected that the sales clairvoyant group will experience the worst result. | — |
Countries
Brazil
Contacts
Public ContactMariana Fava
Universidade de Franca
Outcome results
None listed