Lifestyle Patterns and Glycemic Control

🩺 Protocol Summary

The goal of the proposed study is to evaluate the feasibility and initial efficacy of stabilizing lifestyle behaviors to improve glucose control and body composition in patients with pre-diabetes. The investigator proposes that following stable lifestyle behaviors will improve patients' glucose control, body composition, and liver fat. The results from this study has the potential to impact clinical practice and patient care.

Primary Research Facility: Columbia University Irving Medical Center (New York, New York)

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 Pre-diabetes?

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

Aged 25 Years or older?

🔍 Protocol Specified Minimum Age: 25 Years

Able to attend required clinic visits at Columbia University Irving Medical Center (New York, New York)?

🔍 Logistical Requirement: Site at Columbia University Irving Medical Center

📍 Primary Site Map

Site: Columbia University Irving Medical Center — New York, New York

💰 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.