Storrs, CTNCT07844616Now EnrollingIRB Ready

Obesity (BMI Equal to or >30) Clinical Trial in Storrs, CT

Access cutting-edge obesity (bmi equal to or >30) treatment through this clinical trial at a research site in Storrs. Study-provided care at no cost to qualified participants.

Sponsored by University of Connecticut

Quick Self-Assessment

See if you qualify for this Storrs location

Preparing your pre-screening questions…

Expert Care in Storrs

Access obesity (bmi equal to or >30) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related obesity (bmi equal to or >30) treatment provided free

Apply for This Storrs Location

Check if you qualify for this obesity (bmi equal to or >30) clinical trial in Storrs, CT

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Storrs

    Convenient for CT residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Storrs site if eligible
  4. 4Begin participation

About This Obesity (BMI Equal to or >30) Study in Storrs

The purpose of this intervention study is to investigate the effects of daily egg intake on markers of gut health, high-density lipoprotein (HDL), metabolic, and immune cell profiles in adults with body mass indexes (BMI) in normal and obesity ranges. This study further aims to determine whether egg effects are associated with baseline gut microbiome profiles, and whether egg effects are different between males and females and by BMI status. The study will address the following objectives: Objective 1: Evaluate the effects of daily egg white vs. whole egg intake on gut health, microbiome, and metabolome profiles. Objective 2: Evaluate the effects of daily egg white vs. whole egg intake on HDL composition and function. Objective 3: Evaluate the effects of daily egg white vs. whole egg intake on immune profiles and function in culture (ex vivo). Participants will be asked to consume egg whites and whole eggs on a daily basis for 4-weeks each, and avoid eating eggs for a total of 8 weeks at different points in the study. Participants will be asked to complete surveys about dietary intake and physical activity, as well as provide blood and stool samples throughout the course of the study.

Sponsor: University of Connecticut

Who Can Participate

Inclusion Criteria

18-50 years old (at time of screening)
Premenopausal status for women
Body mass index (BMI) 18.5 to \< 25 kg/m2; or ³ 30 kg/m2 and \>30% and \>40% body fat for men and women, respectively
Willing to consume whole eggs and egg whites provided during the study on a daily basis, and refrain from other eggs or egg-based foods and beverages during the study
Do not fit any

Exclusion Criteria

\<18 years old and ≥ 51 years old
BMI \<18.5, 25-29.9, or body weight \< 110 pounds
Experienced \>10% weight change in the past 4 weeks
Elevated fasting glucose levels (fasting glucose higher than 126 mg/dL) and triglycerides greater than 500 mg/dL, or total cholesterol \< 120 mg/dL and HDL- cholesterol \< 15 mg/dL
Self-reported and/or physician-diagnosed history of severe constipation, diabetes mellitus, coronary heart disease, stroke, renal or liver disease, cancer, eating disorders, certain severe and/or relapsing/remitting autoimmune, inflammatory, intestinal or metabolic diseases, chronic infections, scleroderma, blood clotting disorders, intravenous drug use, or current pregnancy or lactation, postmenopausal
Allergy to eggs
Implanted medical device (e.g., pacemaker) or other health condition that would prevent measurement of body composition by bioelectrical impedence
Currently taking lipid-lowering medications (e.g., statins, fibrates), glucose-regulating medications, anti-inflammatory medications (e.g., NSAIDs, corticosteroids), or medications that primarily affect blood clotting (e.g., warfarin), long-term antibiotics or probiotics in the last 3 months or during the intervention
Active smoker

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Storrs?

Yes, this clinical trial (NCT07844616) has an active research site in Storrs, CT that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Obesity (BMI Equal to or >30) Treatment Options in Storrs, CT

If you're searching for obesity (bmi equal to or >30) treatment options in Storrs, CT, this clinical trial (NCT07844616) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Storrs research site is actively enrolling participants for this clinical trial. You'll receive care from experienced obesity (bmi equal to or >30) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all obesity (bmi equal to or >30) clinical trials near you to find additional studies recruiting in your area.

More Heart Attack Trials in Storrs, CT

See all heart attack clinical trials recruiting in Storrs — not just this study.

Browse Heart Attack Trials in Storrs →

Ready to Join in Storrs?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Storrs, CT