Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT06721351
Eligibility Criteria:
Inclusion Criteria:
1. Capacity to provide informed consent. Individuals must have the capacity to understand the study information, risks, and benefits and voluntarily provide informed consent.
2. Stated willingness to comply with all study procedures and availability for the duration of the study.
3. Established and active patient of SYHealth-CV and KC (having a medical appointment in the last 18 months).
4. Person aged 22 and older.
5. Established diagnosis of DM.
6. Medical appointment(s) (in-person or telehealth) scheduled during the intervention period.
7. Has not completed a dilated eye exam or retinal exam in the last 11months.
Exclusion Criteria:
1. have a prior diagnosis of DR, macular edema, or retinal vascular occlusion;
2. have persistent visual Impairment in one or both eyes;
3. history of ocular injections, laser treatment of the retina, or intraocular surgery (excluding cataract surgery);
4. pregnant women; and
5. diagnosis of mental or degenerative disease that prevents self-consent for the study.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
22 Years
Study:
NCT06721351
Study Brief:
Protocol Section:
NCT06721351