Clinical Trials Directory

Trials / Completed

CompletedNCT02982629

Improving Access to Eye Care in Glaucoma Patients

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
250 (actual)
Sponsor
Wills Eye · Academic / Other
Sex
All
Age
21 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALReminder letter InterventionPatients in this group receive letters and phone calls to reschedule missed follow-up appointments.

Timeline

Start date
2013-03-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2016-12-05
Last updated
2023-12-13

Source: ClinicalTrials.gov record NCT02982629. Inclusion in this directory is not an endorsement.