Obesity & Overweight Clinical Trials
37 studies are recruiting for obesity & overweight in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Feasibility and Acceptability of a Pediatric Referral to Summer Day Camps to Treat Obesity in Children From Low-Income Households
Children from low-income households have a 25-30% higher prevalence of OWOB compared to their higher-income peers. The lack of feasible and effective treatments to address obesity in children with OWOB and from low-income household's points to a real need for prioritization and urgency. The U.S. Pr…
- Stage
- Not phased
- Ages
- 5 to 11
- Site
- University of Central Florida, Orlando, Florida
- Run by
- University of Central Florida
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The Effects of Lumateperone on Obesity and Physiologic Aging and Their Association With Antidepressant Response in Bipolar Depression
This research study examines how a medication called lumateperone may affect mood symptoms, and inflammation in adults with bipolar disorder over approximately 6 weeks. An MRI scan to calculate biological age of the brain will also be obtained at the start of the study.
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
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Effects of Dietary Supplements on Muscle Mass and Function While Using GLP-1 Medication
This pilot study will examine whether daily protein supplementation with or without a mixture of culinary spices can help preserve muscle mass and function in adults who are using GLP-1 medications for weight management. The study will include 75 adults who recently started a GLP-1 medication and a…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- UCLA Center for Human Nutrition, Los Angeles, California
- Run by
- University of California, Los Angeles
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Alpelisib Challenge Test (ACT)
The goal of this study is to test a potentially easier method for measuring how much insulin a person is capable of producing than the current gold-standard method, the "hyperglycemic clamp." Participants will come in for a two-day (overnight) visit in which they will first undergo a "hyperglycemic…
- Stage
- Phase 1
- Ages
- 18 to 70
- Site
- Columbia University Irving Medical Center, New York, New York
- Run by
- Columbia University
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BRIDGE & Friends Trial
Aim 1. Conduct a 6-month (24-session) RCT comparing MedDiet-WL to MedDiet-SN among 268 older adults with obesity (50-79 years, BMI = 30-50 kg/m²). We hypothesize that 1) Participants in MedDiet-SN will show improvements in bodyweight/BMI and body fat compared to MedDiet-WL at post-intervention (6-m…
- Stage
- Not phased
- Ages
- 50 to 79
- Site
- University of Illinois Chicago, Chicago, Illinois
- Run by
- University of Illinois at Chicago
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Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity
The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), mag…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Exponent Phoenix, Phoenix, Arizona
- Locations
- 3 in total
- Run by
- Foundation for the National Institutes of Health
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Comparing the Effects of Front-of-Package Labeling Schemes in Indonesia
The goal of this study is to examine what type of front-of-package label (FOPL) would be most effective at discouraging consumption of products high in nutrients of concern in Indonesia. The main questions this experiment aims to answer are: 1. Would nutrient warning labels be more effective at dis…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Carolina Population Center, Chapel Hill, North Carolina
- Run by
- University of North Carolina, Chapel Hill
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Prebiotic Inulin for Late-Reproductive Individuals
This study aims to evaluate the effects of 2 weeks of inulin supplementation in perimenopausal women with overweight or obesity. The primary questions this study seeks to answer are: 1. Does 2 weeks of inulin supplementation alter the gut and vaginal estrobolome compared with placebo? 2. Does 2 wee…
- Stage
- Not phased
- Ages
- 40 to 55
- Site
- Milken Institute School of Public Health, Washington D.C., District of Columbia
- Run by
- George Washington University
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Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.
Our overarching goal is to adapt and test the PINPOINT intervention -PatIent Navigation for the Prevention of CervIcal CaNcer inTervention. We will test the PINPOINT intervention among patients with high-risk profiles for cervical cancer who do not meet the recommended screening for cervical cancer.
- Stage
- Not phased
- Ages
- 25 and older
- Site
- UF Health Internal Medicine, Gainesville, Florida
- Run by
- University of Florida
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Gestational Response, Outcomes, and Weight After GLP-1 Use
The goal of this observational study is to learn if using GLP-1RA medications for weight loss before pregnancy influences gestational weight gain and pregnancy outcomes. The main aims of the study are to: * Compare gestational weight gain between women with preconception GLP-1RA exposure and those …
- Stage
- Not phased
- Ages
- 18 to 45
- Site
- University of Kansas Medical Center, Kansas City, Kansas
- Run by
- University of Kansas Medical Center
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Tirzepatide Impact Assessment Study
This study examines how two different weight-loss strategies affect heart and metabolic health, as well as changes at the molecular level in the body. One group includes adults who are starting a GLP-1 receptor agonist medication (i.e., semaglutide or tirzepatide) prescribed by their own doctor for…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Nutrition Metabolic Health Initiative (NMHI), Lubbock, Texas
- Run by
- Texas Tech University
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Fast In-Bed Tracking (FIT) System Lifestyle Intervention is a Clinical Trial of a Bed Scale Device. Overweight Wheelchair Users Will Complete a Weight Loss Program, Half Get Scales at Baseline, Half at Month 6 Those Who Receive the Bed Scales at Baseline Are Expected to Have Increased Weight Loss
This project will complete the final design and development steps to commercialize the Fast In-Bed Tracking (FIT) Platform, which is an e-Health and wellness Internet of Things (IoT) monitoring system that can be integrated into a user's bed and provide person-centered, real-world outcomes to suppo…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Pittsburgh, Bakery Square, Department of Rehabilitation Science and Technology, Pittsburgh, Pennsylvania
- Run by
- Jonathan Pearlman
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A Proof-of-Concept Study to Evaluate Topical-Lingual Semaglutide in Adults With Obesity
This study investigates the Topical-Lingual (T-L) delivery of semaglutide, a GLP-1 receptor agonist (GLP-1RA), via an oral liquid emulsion formulation as a Proof-of-Concept for the T-L delivery of metabolic hormones in general. GLP-1 is a gut-derived hormone that induces satiation through hypothala…
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- Clinical Research Institute of Minnesota, Minneapolis, Minnesota
- Run by
- Gila Therapeutics, Inc.
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Determination of Resistance Training Status for Patients on Glucagon-Like Peptide-1 Receptor Agonists
This study examines how adults who take a GLP-1 receptor agonist medication (such as semaglutide [Ozempic, Wegovy, Rybelsus], liraglutide [Saxenda, Victoza], or tirzepatide [Mounjaro, Zepbound]) perform resistance (strength) training before and after starting their medication. GLP-1 medications are…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Ohio State University, Columbus, Ohio
- Run by
- Ohio State University
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Family-Based Weight Wellness Treatment Through Food is Medicine and Group Medical Visits in Pediatric and Adult Primary Care
The proposed project aims to implement and evaluate a novel, family-based lifestyle medicine intervention integrating group Shared Medical Appointments (SMAs) for parents and adolescents with a twelve-month medically tailored groceries (MTG) and six-month culinary medicine Food is Medicine program.…
- Stage
- Not phased
- Ages
- 12 to 17
- Site
- Tufts Medical Center, Boston, Massachusetts
- Locations
- 2 in total
- Run by
- Tufts University
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Pilot Study of "Bottarga" Supplementation: A Little-known, Sustainable "Blue" Food
This pilot study aims to explore the potential benefits of consuming Greek bottarga (grey mullet fish roe) in individuals with at least one metabolic abnormality (low HDL cholesterol, high LDL cholesterol, high triglycerides, obesity, or HbA1c ≥ 5.7%) or a diagnosis of diabetes. Before initiating t…
- Stage
- Not phased
- Ages
- 18 to 60
- Site
- Cambridge Health Alliance, Sommerville, Massachusetts
- Run by
- Cambridge Health Alliance
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Changes in Body Composition Including Muscle With Anti-Obesity Medications, Both With and Without Exercise
The goal of this clinical trial is to learn whether adding either cardiovascular exercise or resistance exercise to pharmacotherapy treatment for obesity improves the retention of lean mass compared to pharmacotherapy alone in adults with overweight or obesity who are prescribed pharmacotherapy for…
- Stage
- Not phased
- Ages
- 18 to 64
- Site
- University of Kansas Medical Center, Kansas City, Kansas
- Run by
- University of Kansas Medical Center
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FIM+DASH: Food is Medicine Intervention to Promote Healthy Eating and Blood Pressure Control
The goal of this clinical trial is to treat both hypertension and obesity in adults using a food is medicine framework. Participants will be randomized 1:1 to FIM+DASH or usual-care control. The 24-week trial includes a 12-week FIM+DASH intervention followed by a 12-week maintenance period and leve…
- Stage
- Phase 2
- Ages
- Any age
- Site
- Mile Square Health Center - South Shore, Chicago, Illinois
- Locations
- 4 in total
- Run by
- University of Illinois at Chicago
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A Study to Evaluate Safety, Tolerability and Pharmacokinetics of Orally Administered TIX100 in Healthy Subjects
Randomized, Placebo-controlled Study to determine the safety and tolerability of multiple oral doses of TIX100 administered daily for 28 days to otherwise healthy overweight/obese subjects.
- Stage
- Phase 1
- Ages
- 18 to 70
- Site
- ProSciento, INC, Chula Vista, California
- Run by
- TIXiMED, Inc.
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Optimizing Self-Monitoring Feedback Delivery for the Treatment of Overweight and Obesity
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.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Advocate Aurora Research Institute, Milwaukee, Wisconsin
- Run by
- Wake Forest University Health Sciences
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A Phase 2A Clinical Trial to Assess the Safety and Tolerability of ERX1000 in Men and Women for the Treatment of Obesity.
The primary objective is to assess the safety and tolerability of oral dose ERX1000 in obese subjects.
- Stage
- Phase 2
- Ages
- 18 to 60
- Site
- Monroe Biomedical Research, Louisville, Kentucky
- Locations
- 3 in total
- Run by
- ERX Pharmaceuticals
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A Study to Evaluate the Safety and Tolerability of Different Doses of CX11 Tablets
A multi-center, randomized, placebo-controlled, double-blinded (within cohorts), Sponsor-unblinded, Phase 1b study to explore the safety, pharmacokinetics, and pharmacodynamics of CX11 tablets in participants with obesity or overweight with weight-related comorbidities.
- Stage
- Phase 1
- Ages
- 18 to 55
- Site
- Corxel Investigational site, Las Vegas, Nevada
- Locations
- 2 in total
- Run by
- Corxel Pharmaceuticals
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Efficacy of Center-based Childcare to Mitigate Unhealthy Weight Gain in Preschoolers From Low-income Households During the Summer
Studies show that preschool-age children are especially vulnerable to accelerated weight gain during the summer, with those from low-income households (≤185% poverty level or Medicaid eligible - the target population for this study) exhibiting the greatest risk of unhealthy weight gain. Despite num…
- Stage
- Not phased
- Ages
- 3 to 5
- Site
- University of South Carolina, Columbia, South Carolina
- Run by
- University of South Carolina
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Hydration Intervention to Decrease Side Effects Associated With GLP - 1 RA Therapy
This is a 17 - week study consisting of a one - week run - in period and a 16 - week intervention. The 16 - week pilot interventions aims to increase hydration in those beginning GLP - 1 RA therapy. Investigators aim to increase hydration to potentially decrease side effect severity, amount of side…
- Stage
- Not phased
- Ages
- 18 to 60
- Site
- State University of New York at Buffalo, South Campus, Buffalo, New York
- Run by
- State University of New York at Buffalo
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Testing a Tailored Approach to Long-Term Weight Loss Success
The purpose of this study is to develop and test an adaptive, individually tailored intervention to prevent weight regain in people who have intentionally lost weight. The main questions it aims to answer are: * Is an adaptive intervention with tailored re-engagement support feasible for individual…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- University of Utah, Salt Lake City, Utah
- Run by
- University of Utah
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.