Patient Navigator Intervention for Vision Impairment or Blindness
(NYCES Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to assist individuals who may be unaware of having high blood pressure (hypertension) or glaucoma. The study will test whether patient navigators, who provide support through text messages, can help participants attend health appointments and learn more about these conditions. Participants will be divided into two groups: one receiving text message support (Intervention Using Patient Navigators) and one without it (Usual Care Without Patient Navigators). This trial suits those aged 40 and older who live in affordable housing and have a cell phone capable of texting. As an unphased trial, it offers a unique opportunity to contribute to research that may enhance healthcare support systems.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What prior data suggests that this intervention using patient navigators is safe?
Research has shown that patient navigator programs have been safely used in various healthcare settings. For example, one study found that a virtual patient navigation program led to fewer hospital visits compared to regular care, indicating that these programs are generally well-received.
Although specific safety data for the navigator program in this trial is not available, these programs typically help people understand and navigate the healthcare system. They focus on providing support and information, not on administering medication or performing medical procedures, which usually makes them low-risk. Overall, existing evidence suggests these programs are safe for participants.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores a new way to support people with vision impairment or blindness through the use of patient navigators. Unlike typical care where patients might only get initial appointment scheduling, this approach offers ongoing text message support for managing follow-up appointments and educating patients about conditions like hypertension and glaucoma. This personalized, continuous assistance could improve adherence to treatment plans and empower patients with valuable health knowledge, which is a big step forward compared to standard care options.
What evidence suggests that this trial's treatments could be effective for vision impairment or blindness?
Research has shown that patient navigators can significantly assist people with visual impairments in maintaining their eye exam schedules. For instance, the NYC-SIGHT Study found that these navigators increased the number of patients attending follow-up eye exams after community screenings. In this trial, participants in the Virtual Automated Navigator Intervention arm will receive text messaging support for scheduling and attending appointments, along with education about hypertension and/or glaucoma. Another study highlighted that patient navigator programs effectively overcome obstacles patients face, facilitating access to necessary care. These findings suggest that patient navigators play a crucial role in managing vision health, particularly for those at risk of glaucoma, a condition that can damage the optic nerve. Meanwhile, participants in the Usual Care arm will only have their initial appointments scheduled without additional support.14678
Who Is on the Research Team?
Lisa A. Hark
Principal Investigator
Columbia University Department of Ophthalmology
Are You a Good Fit for This Trial?
The NYC Eye Study is for adults aged 21+ living independently in certain affordable housing areas. It's aimed at those with eye conditions like blindness, cataract, diabetic retinopathy, and glaucoma. People with terminal illnesses or unable to consent due to dementia cannot participate.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants in the Intervention Arm receive ongoing support from patient navigators for follow-up eye care over a 1-year period.
Usual Care
Participants in the Usual Care Arm receive automated appointment reminders for follow-up eye exams over a 1-year period.
Follow-up
Participants are monitored for adherence to follow-up eye care appointments.
What Are the Treatments Tested in This Trial?
Interventions
- Intervention Using Patient Navigators
- Usual Care Without Patient Navigators
Find a Clinic Near You
Who Is Running the Clinical Trial?
Columbia University
Lead Sponsor