Age-Related Macular Degeneration (AMD) - Usability Study
Completed
- Conditions
- Age Related Macular Degeneration
- Interventions
- Device: Foresee Home
- Registration Number
- NCT00963339
- Lead Sponsor
- Notal Vision Ltd.
- Brief Summary
The purpose of this study is to evaluate the usability of the Foresee Home device with intermediate AMD patients.
- Detailed Description
The AMD usability study is a prospective, longitudinal, multi-center, observational study of patients diagnosed with intermediate (dry) AMD who have been asked by their doctor to use the ForeseeHomeTM device to record the natural progression of their AMD, including conversion from the dry to wet stage.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 54
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Dry AMD Foresee Home subjects diagnosed as intermediate AMD in at least one eye
- Primary Outcome Measures
Name Time Method Successful self tutorial performance 3 months Ability of the subjects to operate the device as define by a successful test completion 3 months Successful unpacking and installation 3 months
- Secondary Outcome Measures
Name Time Method Evaluate the success rate of the interactive tutorial as defined by a reliable test result. 3 month