Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07577765

Testing a Tailored Approach to Long-Term Weight Loss Success

Led by University of Utah · Updated on 2026-05-11

30

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

Sponsors

U

University of Utah

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial 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.

CONDITIONS

Official Title

Testing a Tailored Approach to Long-Term Weight Loss Success

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • BMI of 27 27 prior to weight loss
  • Lost 27 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Utah

Salt Lake City, Utah, United States, 84112

Actively Recruiting

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Research Team

J

Josh Oliver

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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