Paid Clinical Trials for Weight Loss

Candace Kastanis

Written by Candace Kastanis

Chemistry B.S. | UC Davis | Clinical Lab Technician

Updated & Fact Checked 7/24/26

What are paid clinical trials for weight loss?

Person standing barefoot on a digital bathroom scale next to an exercise mat

Paid clinical trials for weight loss are designed to explore treatments that aid in achieving long-term weight loss. Clinical trials that specifically target problems with obesity related diseases aim to find solutions that promote a healthy lifestyle and better patient outcomes. As such, clinical trial sponsors recruit volunteers and pay them for their participation. Paid clinical trials for weight loss provide compensation for time, travel, and any care needs related to the study. They do this to help increase public participation in hopes of attracting more diverse patient populations to their study.

Quick Facts: Paid Weight Loss Clinical Trials

  • Actively recruiting US studies (July 2026): 631 for obesity and 165 for weight loss (ClinicalTrials.gov)
  • Typical compensation: $25–$100 per completed visit; residential metabolic studies pay more
  • Cost to participate: $0 — study medication, visits, and lab work are covered by the sponsor
  • Biggest recruitment driver: GLP-1 and next-generation obesity medications in Phase 3 testing
  • Find one near you: Browse paid clinical trials by state or see obesity clinical trials

2026 Weight Loss Research Updates

  • Next-generation medications are in late-stage trials: retatrutide, a triple-receptor agonist, produced 24.2% average weight loss over 48 weeks in trial results, and its Phase 3 program continues to enroll.
  • Pills are catching up to injections: oral options posted strong Phase 3 results in 2025–2026, including orforglipron (11.2% average loss over 72 weeks) and 25 mg oral semaglutide (13.6% over 64 weeks), expanding the kinds of studies recruiting volunteers.
  • CagriSema awaits FDA review: the semaglutide-cagrilintide combination showed 15–17% average weight loss and has been filed for approval.
  • 631 obesity studies are recruiting across the US as of July 2026, per ClinicalTrials.gov.

How do I find paid clinical trials for weight loss near me?

Based upon your personal risk factors, your physician may suggest a paid clinical trial for weight loss in your local area. We also recommend checking in periodically with state and local government sponsored websites, research hospitals, and educational institutions as they typically have a plethora of current resources for paid clinical trials for weight loss and related genres.

Effects of Brain Stimulation on Food Intake and Behavioral Weight Loss Treatment
Recruiting
This study will determine whether electrical stimulation of an area of the brain called the dorsolateral prefrontal cortex, which is important in determining the feeling of fullness after eating, affects how much food a person eats and weight loss over 4 weeks. It will also compare weight changes in people who attend weight loss counseling sessions and those who do not over this period of time. Obese, non-diabetic people between 18 and 60 years of age who are in good health and who live in the... Read More
Gender:
ALL
Ages:
Between 18 years and 60 years
Trial Updated:
08/09/2025
Locations: NIDDK, Phoenix, Phoenix, Arizona
Conditions: Electric Stimulation Therapy, Obesity, Weight Loss, Eating
Dyad Plus Effectiveness/Feasibility
Recruiting
The purpose of this research is to determine the effectiveness of a coordinated program (Dyad Plus) that would help to facilitate self-monitoring, positive communication, joint problem solving, and social support to increase physical activity, healthy eating, and weight loss. Participants of the Brenner FIT (Families In Training) pediatric weight management program and their parent/guardian will co-enroll in weight loss programs. Parents/guardians will receive the components of By Design Essenti... Read More
Gender:
ALL
Ages:
Between 13 years and 65 years
Trial Updated:
03/28/2025
Locations: Wake Forest Baptist Medical Center, Winston-Salem, North Carolina
Conditions: Weight Loss, Pediatric Obesity, Overweight Adolescents, Parent-Child Relations, Family and Household
Endoscopic Bariatric Therapies (EBTs): A Retrospective and Prospective Multicenter Registry
Recruiting
The purpose of this registry study is to collect data through medical chart review and in patient visits on the efficacy and safety of various Endoscopic Bariatric therapies (EBTs). This is a retrospective and prospective, observational, medical chart review study for at least 6 standard of care visits up to 1 years after a subject consents for study participation.
Gender:
ALL
Ages:
Between 18 years and 89 years
Trial Updated:
05/20/2025
Locations: Weill Cornell Medicine, New York, New York
Conditions: Obesity, Weight Loss, Gastro Esophageal Reflux, Bariatric Surgery Candidate
Exercise Effects on Adipose Tissue Structure and Function
Recruiting
Participants will be randomized into one of two different experimental groups: 1) Exercise group and 2) No exercise (control group). Subject participation in the study will involve a series of metabolic tests before and after participants undergo a 10% weight loss program (with or without exercise training depending on group randomization). After completing this weight loss portion of the study, participants will then be required to adhere to a high calorie diet program to regain half of the wei... Read More
Gender:
ALL
Ages:
Between 18 years and 40 years
Trial Updated:
06/25/2025
Locations: University of Michigan, Ann Arbor, Michigan
Conditions: Obesity, Metabolic Syndrome, Metabolic Disease, Insulin Resistance, Weight Loss, Weight Gain
International Weight Control Registry
Recruiting
The IWCR is a global scientific study aimed at better understanding the opportunities and barriers for reducing the prevalence of obesity by collecting information from people who have experience with weight management in their everyday lives. The investigators seek to gather information on a wide range of weight management experiences, ranging from weight loss and weight loss maintenance to weight gain and inability to lose weight.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/03/2024
Locations: University of Alabama at Birmingham, Birmingham, Alabama +6 locations
Conditions: Weight Loss, Overweight, Obesity
Time-restricted Eating Versus Daily Continuous Calorie Restriction on Body Weight and Colorectal Cancer Risk Markers
Recruiting
Approximately 42% of American adults are obese, and this condition is strongly related to the development of colorectal cancer. Innovative lifestyle strategies to treat obesity and reduce colorectal cancer risk are critically needed. This research will demonstrate that time-restricted eating, a type of intermittent fasting, is an effective therapy to help obese individuals reduce and control their body weight and prevent the development of colorectal cancer.
Gender:
ALL
Ages:
Between 45 years and 70 years
Trial Updated:
07/01/2025
Locations: University of Illinois at Chicago, Chicago, Illinois
Conditions: Time Restricted Eating, Obesity, Weight Loss, Colorectal Cancer
Engaging Men in Weight Loss With a Game-based mHealth and Neurotraining Program
Recruiting
Men in the United States have an exceptionally high prevalence of overweight and obesity, i.e., 71.3%, and 42% of men are currently attempting weight loss. However, men are dramatically underrepresented in weight loss programs. Attempts to modestly adapt standard weight loss programs have seen only minimal success. Mobile applications (mHealth apps) have attractive features, but have low male enrollment and poor efficacy as conventionally delivered. A gamified mHealth program offers the possibil... Read More
Gender:
ALL
Ages:
Between 18 years and 55 years
Trial Updated:
09/05/2023
Locations: Drexel University, Philadelphia, Pennsylvania
Conditions: Obesity, Weight Loss
Choosing Healthy Activities and Lifestyle Management Through Portal Support
Recruiting
The study aims to randomize 250 participants to 1 of 2 arms: a.) an Active Intervention Group (based on the Look AHEAD\* ILI) or b.) a Comparison Group (based on the Look AHEAD DSE Comparison group) to test the hypothesis that a multicomponent, multilevel behavioral weight loss intervention (Active Intervention Group) adapted for underserved groups and delivered through Health Information Technology (Health IT) tools via the Electronic Health Record (EHR) patient portal, will result in significa... Read More
Gender:
ALL
Ages:
16 years and above
Trial Updated:
12/10/2024
Locations: University of Tennessee Health Science Center / Department of Preventive Medicine, Memphis, Tennessee
Conditions: Weight Loss, Overweight and Obesity, Behavior, Health
Weight Loss and Physical Fitness Following Pregnancy in Active Duty Women
Recruiting
Pregnancy and delivery are major stressors on the female body and contribute significantly to permanent weight gain and associated morbidity in women. This can profoundly affect the ability of active duty (AD) women to advance in their career. The first 12 weeks postpartum are the time period during which the most significant weight loss occurs and is critical in achieving a healthy weight in the first year postpartum. Many factors contribute to effective weight loss in this period among which t... Read More
Gender:
FEMALE
Ages:
Between 18 years and 44 years
Trial Updated:
05/16/2024
Locations: Tripler Army Medical Center, Honolulu, Hawaii +1 locations
Conditions: Weight Loss, Postpartum Weight Retention
BrainWeighve Weight Loss App
Recruiting
Childhood obesity within the United States has been a growing concern over the past number of years, and if not addressed, leads to detrimental health outcomes for youth as they move into adulthood. The literature suggests that over-eating, especially when framed in terms of food addiction, plays a key role in this epidemic; however, treatment options are time intensive, posing a profound logistical barrier for both the child and parent and often limits or prevents engagement. As research within... Read More
Gender:
ALL
Ages:
Between 14 years and 18 years
Trial Updated:
11/21/2023
Locations: UCLA Integrated Substance Abuse Programs, Los Angeles, California
Conditions: Weight Loss

Who conducts paid clinical trials for weight loss?

There is a great deal of momentum to find better ways to treat obesity-related illnesses. Pharmaceutical companies continue to develop new drug therapies targeted towards achieving weight loss in individuals who are over the recommended BMI. Therefore, various clinical trial sponsors routinely host paid clinical trials dedicated to studying the effectiveness of these drug candidates before they can be entered into the clinical market.


What kinds of paid weight loss studies are there?

Weight loss research covers more than new medications. Depending on your health profile, you may qualify for several study types, each with its own pay structure and time commitment:

Study typeTypical payWhat is involved
Medication trials (GLP-1 and next-generation drugs)$50–$100 per visit48–72 weeks of visits with lab work and weigh-ins
Lifestyle and behavioral studies$25–$75 per visitDiet, exercise, or coaching programs with regular check-ins
Residential metabolic studiesHigher total pay, set per protocolDays to weeks at a research unit with a fully controlled diet
Device and post-surgical studies$50–$150 per visitFollow-up visits after a procedure or while using a monitored device
Remote and app-based studies$10–$50 per taskFood logging, surveys, or wearable data from home

Every study sets its own compensation, and the exact schedule appears in the consent form before you enroll.

Can I join a trial if I already take Ozempic, Wegovy, or Zepbound?

Usually not right away. Most medication trials exclude people who have recently used a GLP-1 drug, and protocols commonly require a washout period of 90 days or more before screening. Some lifestyle, device, and long-term follow-up studies do accept current or former GLP-1 users, so it is worth asking the coordinator rather than ruling yourself out. Always tell the screening team about any weight loss medication you take, including compounded versions.

Will I get a placebo instead of the real drug?

In most Phase 3 weight loss trials, some participants receive a placebo, and neither you nor the study team chooses who. Two things soften that: everyone in these trials typically receives structured lifestyle counseling at no cost, and many programs offer an open-label extension where placebo participants can receive the active drug after the main study ends. The consent form states the odds of receiving placebo before you enroll.

What are the advantages of participating in paid clinical trials for weight loss?

Obesity related illnesses are responsible for approximately 200.000 deaths per year. (Source: NIH) Participating in a paid clinical trial for weight loss allows you to gain access to potentially lifesaving interventions while also being compensated.


What are the disadvantages of participating in paid clinical trials for weight loss?

You may need to make significantly changes in lifestyle to achieve the objectives of the clinical trial. You may also need to attend regular check ins and testing appointments to fulfill the requirements for the paid clinical trial you are participating in. This equates to time and adherence to outlined expectation to receive full compensation values. Other disadvantages may relate to adverse side effects and discomfort from any drug therapies administered during the trial. The most significant downside to participating in a paid clinical trial for weight loss might be disappointment if the therapeutic intervention fails to work as expected.


How do paid clinical trials for weight loss work?

The benchmark for participating in a clinical trial for weight loss is the qualification process. The principal investigator will want to establish you as a viable candidate. This may require pretesting procedures and behavioral evaluations prior to being accepted into the study. Depending on the type of paid study you are participating in, you may be asked to speak with a behavioral health specialist to discuss your personal history of obesity related challenges.

Upon successful enrollment, you will receive medications, medical testing, and any necessary health care expenditures pertaining to the paid clinical study for zero out of pocket costs once successfully enrolled.

The clinical study pathway involves four study classifications to help determine if a new therapeutic is safe for human use.

Weight loss trials move through the same four FDA-regulated phases as any other study: Phase I establishes safety and dosing (usually with healthy volunteers, and typically the highest paying), Phases II and III test how well the treatment works in progressively larger groups, and Phase IV monitors long-term safety after approval. Our guide to the types of paid clinical trials explains each phase and what to expect as a participant.


What do researchers learn from conducting paid clinical trials for weight loss?

By conducting paid clinical trials for weight loss, researchers can better understand the reasons why certain Indvidual’s may experience more difficulties losing weight as compared to others. You, as a participating patient assist in this process by contributing your information and personal experience by way of the clinical study intervention being studied.

The research community has access to clinical study trial findings all over the globe by what is often to referred to as big data. Biological data banks and biorepositories allow researchers to study a wealth of information for the purpose of developing improved health strategies, drugs, and therapeutics. Collectively, the type of information acquired may include:

  • Historical health history
  • Familial health history
  • Genetic profiles
  • Age
  • Bio-gender
  • Lifestyle
  • Behavioral
  • Drug use
  • Alcohol consumption
  • Supplement use
  • Mental health
  • Cognitive abilities
  • Sensory integration intelligence

Commonly Asked Questions (FAQs)

  • How much are participants compensated in paid clinical trials for weight loss?

    Most outpatient weight loss studies pay $25–$100 per completed visit, and many also cover meals, coaching, or lab work at no cost. Residential metabolic studies, where you stay at a research unit while your diet is controlled, pay considerably more. The exact amount depends on the trial type and sponsor and is listed in the consent form.

    As a clinical trial participant, you will be expected to engage in routine check-ins, testing, evaluations, and may be asked in return to perform various health-related tasks. It is common when participating in a paid clinical trial for weight loss for patients to be required to:

    • To maintain a health diary or journal
    • Adhere to medication schedules
    • Allow for routine lab tests for the duration of the trial
    • Allow for neurological testing
    • Engage in behavioral therapy
    • Maintain availability for any group weight-loss therapies
    • Lose a certain amount of weight in a specified time interval

  • How do I find out if I am eligible to participate in a paid clinical trial for weight loss?

    The eligibility criteria may vary according to the clinical trial type and sponsor. However, since the aim is directed at weight loss, you as a patient may need to have a demonstrated long-term problem with obesity. Pre-existing health and risk factors also contribute to the selection criteria as they would like to ensure a safe experience.

    Eligibility for paid clinical trials for weight loss may depend on your personal health information related to:

    • Age preferences
    • Gender
    • Occupation
    • Lifestyle
    • Preexisting health challenges
    • Long-term goals
    • Health history

  • Will participation in a paid clinical trial for weight loss prevent me from leaving prior to completion?

    Participation in any clinical trial is strictly voluntary. You can leave at any time for any reason, however, leaving early could affect compensation. Often, paid clinical participants choose to leave because of family obligations, or unforeseen circumstances of some kind. It is in the clinical sponsors best interest for all participants to complete the trial objectives successfully. So, you should expect a lot of cooperation on their part to help you finish without any hiccups.

  • What type of information is normally collected in paid clinical trials for weight loss?

    For those interested in participating in paid clinical trials for smokers, you should expect information requests as it pertains to lifestyle, family history, etc. Researchers will use this information to determine if you are a good fit for the study.

    Once determined eligible and you move forward in the trial process, patients typically must submit to routine laboratory testing alongside other necessary treatment modalities. Testing and any information learned along the way, helps to keep you safe and measure the effectiveness of the drug interventions being studied.

  • How long do paid clinical trials for weight loss usually last?

    Clinical trials do not have set timelines and vary from study to study. Clinical trial lengths are dependent upon a series of ongoing factors such as:

    • Patient recruitment and retention
    • Patient health
    • The type of paid clinical trial I.e., randomized, double-blind
    • Adverse health reactions or results
    • Post-clinical trial care and follow-ups

  • If I am interested in participating in a paid clinical trial for weight loss, what questions should I ask?

    Clinical trial investigators must disclose all relative information about the paid clinical trial you are enrolled in and any inherent risk factors. This disclosure process is called informed consent.

    The NIH maintains clear guidance for the structure and safety of clinical trial execution. There is a strict emphasis on patient safety, and as such, an informed consent disclosure must include the following information:

    1. The comprehensive nature of the treatment, procedure, or drug.
    2. Any inherent risks associated with the intended treatment methods.
    3. Reasonable alternatives to the procedure or treatment intervention.
    4. Assessment and acknowledgment that you understand items 1-3.

    Informed consent is required and articulates the agreement between you, your healthcare physician, and clinical trial sponsors. The purpose of informed consent is to provide the patient with the details of every facet of the intended clinical trial study plan. This goal of informed consent is to establish trust and confidence between the eligible participant and the clinical trial sponsor team leads.

    Key things to ask the coordinator: the goal of the study, whether you could receive a placebo, expected side effects, the exact compensation and payment schedule, what costs are covered, and what happens if you leave early.