Testing a Tailored Approach to Long-Term Weight Loss Success
University of Utah · with National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · NCT07577765
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 30
- US sites recruiting
- 1
- Study start
- January 7, 2026
- Record last updated
- May 11, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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 individuals following intentional weight loss?
- Does this intervention prevent weight regain after intentional weight loss?
Participants will
- Complete a baseline assessment of body measurements
- Complete surveys on dietary intake, mental health, and physical activity
Participants will also engage in a 26-week program, which involves:
- Receive regular educational texts/emails
- Fill out weekly online survey check-ins
- Weigh themselves at least weekly on a scale provided by the study
- Some participants may receive health coaching during portions of the study.
- Assessments will be repeated for all participants at the end of the intervention period.
Being studied: Adaptive weight regain prevention
Conditions: Weight Loss; Weight Regain; Obesity & Overweight
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- BMI of ≥ 27 prior to weight loss
- Lost ≥ 7% of body mass in the past 6 months
- Weight loss was intentional
- No plans for weight loss surgery in the next 6 months
- Access to a smart device that can download applications and receive text messages
- Able to receive clearance for study participation from primary care provider
Exclusion Criteria
- Pregnant or within 12 months postpartum, or planning pregnancy
- Uncontrolled conditions that affect overall health (cardiovascular, metabolic, renal, pulmonary, psychiatric, thyroid, cancers)
- Food insecure
- Bariatric surgery or cancer treatment within the past 5 years
- Active or recent (\<12 months) treatment/diagnosis of an eating disorder
Recruiting US locations
University of Utah
Salt Lake City, UT 84112
Site contact: Josh Oliver · 971-645-6693 · joshua.oliver@hsc.utah.edu
Study contacts (from the official record)
- Josh Oliver · 971-645-6693 · joshua.oliver@hsc.utah.edu
Similar studies in Utah
All weight loss studies in Utah →- RecruitingHealthy volunteersPhase 1
Study of GS-4571 in Healthy Participants, Nondiabetic Obese Participants, and Nonobese Participants With Type 2 Diabetes Mellitus (T2DM)
Gilead Sciences
- Location
- Salt Lake City, UT + 2 other US sites
- Eligibility basics
- Ages 18–65
- RecruitingPhase 1
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Two Formulations of ASC36 Injection in Participants With Obesity or Overweight
Ascletis Pharma (China) Co., Limited
- Location
- Salt Lake City, UT + 1 other US site
- Eligibility basics
- Ages 18–65
- RecruitingPhase 2
Study to Assess the Effect and Safety of ALV-100 on Maintenance of Weight Loss
Alveus Therapeutics, Inc.
- Location
- South Jordan, UT + 19 other US sites
- Eligibility basics
- Ages 18–75
- RecruitingPhase 3
A Clinical Study to Evaluate the Effects of Enicepatide (RO7795068) in Participants With Obesity or Overweight Without Type 2 Diabetes
Hoffmann-La Roche
- Location
- Salt Lake City, UT + 43 other US sites
- Eligibility basics
- Ages 18+