Remote training and tiny sensors could revolutionize low vision care
NCT ID NCT06107881
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study compares telerehabilitation (remote training) to in-office care for adults with low vision who have received new magnification devices or assistive apps. Researchers will also use Bluetooth sensors to monitor if patients stop using their devices, aiming to provide timely support. The goal is to improve quality of life by making reading and daily tasks easier, while overcoming barriers like travel and lack of specialists.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low vision rehabilitation (training with magnification devices and assistive mobile apps)
- What this could lead to
- If successful, this could make low vision training more accessible via remote sessions, improving daily reading and tasks for many people.
- What could go wrong
- This is a behavioral study, not a drug trial, so benefits may be modest. Results depend on participant engagement and may not apply to all types of vision loss.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 350 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2023
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adults with any level of vision loss due to any ocular disease who are age 18 and older, and who have received new magnification device(s) for the first time (i.e., hand-held optical magnifiers, portable electronic video magnifiers, high near add powers of +4.00 or greater, visual assistive mobile apps for their smartphone/tablet, some stand magnifiers and CCTVs) from one of our participating low vision rehabilitation sites at the four academic centers and one private practice. Exclusion Criteria: * schedules not permitting participation in planned study visits (including planning to move far from their clinical provider's office within the first 4-months of the study (i.e., cannot attend in-office visits) or take extended vacation that would not allow them to complete study procedures during the first four months of the study period), * inability to understand study procedures or communicate responses to visual stimuli in a consistent manner (greater than mild cognitive impairment as per TICS), * substance abuse, * significant hearing loss (unable to hear communication by phone or via videoconferencing), * significant medical condition likely to limit participation or lifespan, * individuals who require other types of LVR training or intervention (e.g., psychosocial). * For Bluetooth low energy beacon sensors, exclusion would occur if 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), (2) no surface area of at least 1"x1" to which the beacon sensor could be attached without interfering with the device, or (3) use of visual assistive mobile apps only.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
9 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Boston University Eye Associates, Inc.
NOT_YET_RECRUITINGBrockton, Massachusetts, 02301, United States
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Chan Family Optometry
NOT_YET_RECRUITINGGrass Valley, California, 95945, United States
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Frank Stein & Paul S. May Center for Low Vision Rehabilitation at The Eye Institute
NOT_YET_RECRUITINGSan Francisco, California, 94102, United States
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Mid-Michigan Eye Care
NOT_YET_RECRUITINGMidland, Michigan, 48640, United States
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New England College of Optometry
NOT_YET_RECRUITINGBoston, Massachusetts, 02115, United States
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See What You Miss Optometry
NOT_YET_RECRUITINGSanta Monica, California, 90401, United States
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Southern Califonia College of Optometry
NOT_YET_RECRUITINGFullerton, California, 92831, United States
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UCLA Stein Eye Institute
RECRUITINGLos Angeles, California, 90095, United States
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University of Nebraska: Weigel Williamson Center for Visual Rehabilitation at the Truhlsen Eye Institute
NOT_YET_RECRUITINGOmaha, Nebraska, 68198, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New High-Tech glasses could help kids with low vision read better
- Virtual reality could help track vision rehab progress
- Can your eyes trip you up? study watches how vision changes stepping over obstacles
- Sound-based wearable could help blind people 'see' obstacles