None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy subjects of either gender Willing to provide informed consent Willing to follow the study procedures
Exclusion criteria
Exclusion criteria: 1.Presence of any acute/chronic illness at the time of participation 2.History of intake of any medication within a week prior to participation in the study 3.Unlikely to comply with the study requirements as per the opinion of the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Measure the visual SRT at three different times of a day 2.Determine the presence of any difference in the variability of visual SRT within gender 3.Compare the visual SRT between males and females 4.Determine the presence of any difference in the variability of visual SRT between genders Timepoint: 3 time points | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Determine the presence of any difference in the variability of visual SRT within genderTimepoint: 3 time points | — |
Countries
India
Contacts
Kasturba Medical College Mangalore