The aim of the research project is to validate the use of a novel functional assessment tool designed to document how participants with a vision impairment complete activities of daily living in a real world environment.
Willing to provide signed informed consent.
Be available for study visits.
Willing to comply with study assessments.
In good general health and ambulant.
Significant co-morbidities which prohibit involvement in study visits.
Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.
Cognitive deficiencies, including dementia or progressive neurological disease.
Have a psychiatric condition that, in the investigator's opinion, precludes compliance with the protocol including past or present psychoses and bipolar disorder.