Socially Assistive Robots to Enhance Magnification Device Use for Reading
NCT ID: NCT04190134
Last Updated: 2024-07-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE1
20 participants
INTERVENTIONAL
2022-04-22
2025-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Immediate Robot
One month after study entry, participants will receive the robot at home for two months, followed by a three month observation period without the robot.
Socially Assistive Robot for Low Vision Rehabilitation
A socially assistive robot will be customized to engage in dialog and conversations to motivate and encourage optimal use of new magnification devices for reading at home by individuals with vision loss.
Delayed/Waitlist Robot
Three months after study entry, participants will receive the robot at home for three months.
Socially Assistive Robot for Low Vision Rehabilitation
A socially assistive robot will be customized to engage in dialog and conversations to motivate and encourage optimal use of new magnification devices for reading at home by individuals with vision loss.
Interventions
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Socially Assistive Robot for Low Vision Rehabilitation
A socially assistive robot will be customized to engage in dialog and conversations to motivate and encourage optimal use of new magnification devices for reading at home by individuals with vision loss.
Eligibility Criteria
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Inclusion Criteria
* age 18 and older,
* received a magnification device(s) (i.e., hand-held optical magnifiers, portable electronic video magnifiers, some stand magnifiers and CCTVs) from the UCLA Vision Rehabilitation Center.
Exclusion Criteria
* inability to understand study procedures or communicate responses to visual stimuli in a consistent manner (cognitive impairment as per TICS),
* substance abuse,
* significant hearing loss (unable to hear communication by phone or from robot),
* significant medical condition likely to limit participation or lifespan,
* their magnifier device has features that would not work in conjunction with the beacon sensors: (1) hands-free and do not have a place where the patient's hand is holding the device during use (therefore, they would not register a significant change in temperature), and/or (2) no surface area of at least 1"x1" to which the beacon sensor could be attached without interfering with the device.
18 Years
ALL
No
Sponsors
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University of Southern California
OTHER
University of California, Los Angeles
OTHER
Responsible Party
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Ava K. Bittner, OD, PhD
Principal Investigator
Principal Investigators
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Ava K Bittner, OD, PhD
Role: PRINCIPAL_INVESTIGATOR
UCLA Stein Eye Institute; Vision Rehabilitation Center
Maja J Mataric, PhD
Role: PRINCIPAL_INVESTIGATOR
USC Interaction Lab; Viterbi School of Engineering
Locations
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UCLA Stein Eye Institute
Los Angeles, California, United States
Countries
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Central Contacts
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Facility Contacts
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Ava K Bittner, OD, PhD
Role: primary
Other Identifiers
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19-001429
Identifier Type: -
Identifier Source: org_study_id
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