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Financial Incentives for Glaucoma Care Adherence
N/A
Waitlist Available
Led By Christopher A Girkin, MD, MSPH
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Anyone ≥ 18 years with a glaucoma associated diagnosis
Non-Hispanic white ≥50 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the time frame will be from baseline through 3 years of recruitment in the study.
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new way to detect and manage glaucoma, using telemedicine to improve access to care for a vulnerable population.
Who is the study for?
This trial is for adults over 18 with glaucoma-related diagnoses, diabetes, or a family history of glaucoma. It focuses on African Americans and Hispanics over 40, and non-Hispanic whites over 50. Participants must speak and understand English. There are no specific exclusion criteria.
What is being tested?
The study is testing if giving people money can make them more likely to go to eye care appointments after being referred for conditions like cataract, glaucoma, diabetic retinopathy, etc., compared to not offering money.
What are the potential side effects?
Since this trial involves financial incentives rather than medical treatments or drugs, there are no direct physical side effects associated with the interventions being tested.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 or older and have been diagnosed with glaucoma.
Select...
I am a non-Hispanic white person aged 50 or older.
Select...
I am 18 or older and have diabetes.
Select...
I can speak and understand English.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ the time frame will be from baseline through 3 years of recruitment in the study.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the time frame will be from baseline through 3 years of recruitment in the study.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Percentage of participants that adhere to referral appointment
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: No financial incentiveExperimental Treatment1 Intervention
This group will receive standard of care eye health education alone and no financial incentive for completing a referral visit.
Group II: Financial incentiveExperimental Treatment1 Intervention
This group will receive a financial incentive once the referral visit is completed (if one was required) as well as eye health education.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Financial Incentive
2016
N/A
~133420
Find a Location
Who is running the clinical trial?
Centers for Disease Control and PreventionFED
887 Previous Clinical Trials
21,992,457 Total Patients Enrolled
University of Alabama at BirminghamLead Sponsor
1,642 Previous Clinical Trials
2,331,569 Total Patients Enrolled
3 Trials studying Refractive Errors
440 Patients Enrolled for Refractive Errors
Christopher A Girkin, MD, MSPHPrincipal InvestigatorUniversity of Alabama at Birmingham
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am African American or Hispanic and 40 years old or older.I am 18 or older and have been diagnosed with glaucoma.I am a non-Hispanic white person aged 50 or older.I am 18 or older and have diabetes.Not applicable.I can speak and understand English.I am 18 or older with a family history of glaucoma.
Research Study Groups:
This trial has the following groups:- Group 1: No financial incentive
- Group 2: Financial incentive
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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