Feasibility of a Nutrition Intervention for Patients With Prediabetes at a Federally Qualified Health Center

🩺 Protocol Summary

The purpose of the study is to assess the feasibility and acceptability of incorporating hands-on nutritional demonstrations to enhance the Diabetes Prevention Program (DPP) curriculum among patients who are at-risk for prediabetes

Primary Research Facility: Cedars-Sinai Medical Center (Los Angeles, California)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Prediabetic State?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged between 18 Years and 99 Years?

🔍 Protocol Specified Age Range: 18 Years to 99 Years

Able to attend required clinic visits at Cedars-Sinai Medical Center (Los Angeles, California)?

🔍 Logistical Requirement: Site at Cedars-Sinai Medical Center

📍 Primary Site Map

Site: Cedars-Sinai Medical Center — Los Angeles, California

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.