NCT07605468Not yet recruiting
Feasibility Study of a Remote Behavioral Dietary Intervention in Patients With Early to Intermediate AMD: Glucose Lowering for Vision Extension
Nonrandomized, Unmasked Feasibility Study of a Remote-based Behavioral Dietary Intervention in Patients With Early to Intermediate AMD: Glucose Lowering for Vision Extension (GLOVE)
Source: ClinicalTrials.gov · Last updated 26 May 2026
Brief summary (registry, in English)
The primary goal of the study is to test dietary intervention at glycemic control and carotenoid levels in participants with intermediate age-related macular degeneration.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- First submitted
- 18 May 2026
- Start date
- Jun 2026
- Primary completion date
- Jun 2028
- Lead sponsor
- Stanford University
- Diseases
- Macular degeneration
- NCT number
- NCT07605468
What you commit to
- Study type: Interventional
- Planned participants: 32
- From Jun 2026 to the primary completion date, Jun 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Use of statins, niacin or other lipid/cholesterol modifying medications
Other illness
- Diabetes or medications used to treat diabetes or obesity (including GLP1 agonists, metformin, glyburide
- Recent cancer (within past 3 years)
Lab values
- HbA1c greater than 6.5%,
Other
- Other retinal or ocular pathology (other than pseudophakia and/or refractive error (between -8 to +8 diopter spherical equivalence)
Who the study is looking for
- Diagnosis of early to intermediate AMD with no history of retinal geographic atrophy (cRORA) or exudative disease
- Eating a diet less healthy than average (Healthy Eating Index \[HEI\] score \<61) based on 3 24-hour dietary recalls
- Access to a computer or smart phone for use in the behavioral meetings (we will provide loaners for those lacking a smart phone
- Because the initial questionnaires (ASA24), surveys and informed consent will be on line and in English, only individuals with fluency in English will be included. (They do not need to list English as their primary language.)
Age in the registry: 55 years to 75 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of California, Los Angeles Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.