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Pilot Testing an Adaptive Intervention for Weight Loss Maintenance

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

• 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

Locations
United States
Utah
University of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Josh Oliver
joshua.oliver@hsc.utah.edu
971-645-6693
Time Frame
Start Date: 2026-01-07
Estimated Completion Date: 2027-09-01
Participants
Target number of participants: 30
Treatments
Experimental: Adaptive Intervention
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Leads: University of Utah

This content was sourced from clinicaltrials.gov