Take Control of Your Health, Join an Obesity Research Study Today!

Participate in innovative clinical trials for obesity and gain access to potential new treatments not available elsewhere. Our studies provide personalized care from experienced medical professionals, guiding you through each step while exploring cutting-edge therapies to support your health.

Your participation can make a real difference—for yourself and for others affected by obesity. By contributing to medical research, you help advance treatments that could improve lives and shape the future of obesity care.

AdobeStock_641318853-1

About the Study 

These clinical research studies are designed to evaluate the safety and effectiveness of potential new treatments for obesity. We currently have multiple study opportunities available, offering participants the chance to work closely with experienced medical professionals and receive comprehensive care throughout their participation.

The studies involve a series of scheduled visits that include health assessments, progress tracking, and personalized guidance. Compensation for study-related time is available, and by participating, you help researchers gain a deeper understanding of obesity and support the development of innovative therapies that may improve health outcomes for millions of people.

Why Should I Participate?

Those who qualify and choose to participate could receive: 

Access to the investigational

medication at no cost  

Access to our top-tier team of board-certified physicians at no cost  

Compensation for study-related time and travel.

Study Criteria 

To qualify to participate you must: 

  • Be aged 18 years or older  
  • Have a BMI greater than 27  
  • Have never had a weight loss surgery 
  • Additional criterion applies
AdobeStock_1789008087 (1)-1

 

Frequently asked questions

What is a research study or clinical trial?

A research study or clinical trial is the process a potential new drug, device, procedure, or process goes through to prove that it is safe, tolerable and effective for the condition it is being studied for. Research studies are the only way to advance medicine for future generations. 

Who can participate in a research study?

Each study has its own set of inclusion and exclusion criteria that a participant must meet before they are allowed to participate in a study. Patients from all backgrounds and walks of life are encouraged to participate.  

What is Informed Consent?

Every participant in every research study must go through the informed consent process. During this, the trial doctor and research team go over what will happen in the study, what treatments you might get, how long the trial is expected to last, what happens during visits, the potential risks and benefits, and many other important facts about the study. Participants may withdraw their consent and discontinue the study at any time for any reason. 

What is a Placebo?

A placebo looks like a treatment but does not have any active medicine in it. Researchers use placebos to help make sure any changes in the participants’ health are actually caused by the study treatment. You do not get to choose if you get the study treatment or the placebo, and you may not know if you get the placebo until after the study. Not all research studies use a placebo. 

Why is Diversity Important?

If studies do not include diverse participants, we cannot know if treatments work for everyone who needs them. Studies only tell researchers how something works for the participants of that study, and they may not work the same in people of different races, ethnicities, ages, or sexes. 

How am I Protected?

All research studies must follow federal laws and ethical guidelines, including HIPAA. Studies must also be approved by an expert group called an institutional review board (IRB) that helps make sure the trial is fair and as safe as possible, and that any risks to the participants are worth the potential benefits.