Milwaukee, WINCT07227051Now EnrollingIRB Ready

Obesity & Overweight Clinical Trial in Milwaukee, WI

Access cutting-edge obesity & overweight treatment through this clinical trial at a research site in Milwaukee. Study-provided care at no cost to qualified participants.

Sponsored by Wake Forest University Health Sciences

Quick Self-Assessment

See if you qualify for this Milwaukee location

Preparing your pre-screening questions…

Expert Care in Milwaukee

Access obesity & overweight specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related obesity & overweight treatment provided free

Apply for This Milwaukee Location

Check if you qualify for this obesity & overweight clinical trial in Milwaukee, WI

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Milwaukee

    Convenient for WI 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 Milwaukee site if eligible
  4. 4Begin participation

About This Obesity & Overweight Study in Milwaukee

The purpose of this research study is to learn how to best provide weekly feedback on individual progress toward intervention goals during a weight loss program.

Sponsor: Wake Forest University Health Sciences

Who Can Participate

Inclusion Criteria

Age greater than or equal to 18 years
BMI greater than or equal to 25.0 kg/m2
Weight less than or equal to 175 kg (due to scale limit)
Own a smartphone compatible with Fitbit (e.g., an Apple iPhone running iOS 16.4 or higher or Android smartphone running Android 11 or higher) with a cellular and data plan

Exclusion Criteria

Weight greater than 175 kg (due to a weight limit of the study-provided scale)
Smartphone device owned deemed incompatible with the Fitbit App
History of bariatric surgery or plans to obtain bariatric surgery during the study period
Current use of weight loss medications, or use of weight loss medications in the 6 months prior to initial pre-screening
Currently participating in a weight-loss program
Weight loss of greater than or equal to 10 lbs in the 6 months prior to initial pre-screening
Physical limitations that prevent walking at a brisk pace for at least 10 minutes without stopping
Use of a pacemaker or other implanted medical device
Currently pregnant
Currently breastfeeding
Less than 1-year post-partum
Plans to become pregnant within the study period
Lack of written confirmation that the potential participant has discussed study participation with their physician if they have been diagnosed with diabetes, hypertension, or has have a history of coronary heart disease
One or more study participants living in the household (enrollment limited to one participant per household)
Medical conditions that contraindicate weight loss or prevent completion of the study (e.g., current diagnosis of cancer or terminal illness, dementia, etc.)
Recent (in the past 6 months) changes in medications that affect weight
Self-reported eating disorder within past 5 years
Unable to complete the 17-week study (due to plans to relocate during the study period, etc.)
Unable or unwilling to provide informed consent
Unable to read English at the 5th grade level
Unwilling to accept random assignment
Unable or unwilling to download the study smartphone application, wear the physical activity monitor, or use the study e-scale
Failure to complete baseline assessment measures
Failure to complete at least 4 out of 6 days of self-monitoring dietary and weight self-monitoring during the behavioral run-in period
Any other condition(s) which, in the opinion of the Principal Investigator, would adversely affect participation in the study

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 Milwaukee?

Yes, this clinical trial (NCT07227051) has an active research site in Milwaukee, WI 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 & Overweight Treatment Options in Milwaukee, WI

If you're searching for obesity & overweight treatment options in Milwaukee, WI, this clinical trial (NCT07227051) 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 Milwaukee research site is actively enrolling participants for this clinical trial. You'll receive care from experienced obesity & overweight 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 & overweight clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Milwaukee, WI