Testing a new way to record daily tasks in people with vision loss
Checks a new tool that records how people with eye diseases manage daily tasks.
Plain-language title generated from the registry record
Registry title: Functional Assessments in Vision Impairment
Key facts
- Where
- Melbourne, AustraliaSee the site
Where in Australia
- Centre for Eye Research AustraliaMelbourne, AustraliaNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Center for Eye Research Australia
- Trial code
- NCT06908161
- Record updated
- 3 April 2025
- Original description
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.Read full original descriptionShow less
A Novel Approach for Capturing Real-world Functional Assessment Outcomes in Participants With a Vision Impairment
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.
Inclusion: Willing to provide signed informed consent; Be available for study visits; Willing to comply with study assessments; In good general health and ambulant; Aged over 18 years of age; Have a vision impairment caused by any ocular condition which affects independent mobility; Agree to allow the research team into their home and local environments; Participate in assessments in public settings.
Exclusion: 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; 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; Deafness or significant hearing loss; Inability to converse in English.