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Improving Access to Eye Care in Glaucoma Patients

Improving Access to Eye Care in Glaucoma Patients a Prospective, Controlled, Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02982629
Enrollment
250
Registered
2016-12-05
Start date
2013-03-31
Completion date
2013-11-30
Last updated
2023-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Keywords

Glaucoma, Eye Care, Community Outreach

Brief summary

1. To design and develop a prospective, randomized pilot study utilizing information from electronic medical records to address follow-up adherence and reduce the gap between recommended and actual follow-up adherence in patients with glaucoma. 2. To evaluate the impact of a telephone-based intervention on follow-up adherence in patients with glaucoma using a randomly assigned comparison with usual care.

Detailed description

The Wills Eye Health System (WEHS) proposes to conduct a pilot study to evaluate the feasibility and effectiveness of a telephone-based intervention to improve rates of follow-up exams in patients with glaucoma. The prospective, randomized, controlled trial entitled Improving Access to Eye Care in Patients with Glaucoma will utilize cohort data from 2013 electronic medical record information to reduce the gap between recommended and actual follow-up utilization of eye care services in glaucoma patients. Patients with glaucoma will be recruited from the Wills Eye Glaucoma clinic who were seen between 3/1/13 and 10/31/13. A recall list will be generated for patients who have scheduled follow-up appointments from 9/1/13 to 11/30/13. These patients will be randomly assigned to the Usual Care group or Intervention group. The primary outcome will be successful attendance at a follow-up appointment within an appropriate time frame. This intervention is based on a CDC funded project at Wills to improve access to eye care in patients with diabetes. Thus, this pilot study will test the efficacy of a telephone-based intervention to improve follow-up adherence in patients with glaucoma by improving access to eye care.

Interventions

BEHAVIORALReminder letter Intervention

Patients in this group receive letters and phone calls to reschedule missed follow-up appointments.

Sponsors

Thomas Jefferson University
CollaboratorOTHER
Wills Eye
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Attended Wills Eye Glaucoma Clinic from 9/1/12 and 10/31/13

Exclusion criteria

* Any medical condition that would preclude the subject from providing reliable and valid data. * Recommended to f/u in less than 1 month time period.

Design outcomes

Primary

MeasureTime frameDescription
Adherence to Follow-Up28 weeksWhether patients adhere to follow-up appointments at 28 weeks.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026