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Life sciences · Interventional Study
ClinicalTrials.gov · November 3, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
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Registry record from ClinicalTrials.gov (NCT06393725). This is a study registration, not published results. Lead sponsor: University of Connecticut. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 378 participants (ESTIMATED). Conditions: Obesity. Interventions: BEHAVIORAL: Asynchronous Remote Lifestyle Intervention; BEHAVIORAL: Synchronous Remote Lifestyle Intervention. Primary outcome measures: Percent of baseline weight loss at 6 months , 6 months; Percent of baseline weight loss at 12 months , 12 months. Brief summary: The goal of this clinical trial is to learn if a group-based digital weight loss program that is delivered asynchronously (via an online platform) is as effective as one that is delivered synchronously (via weekly videoconference meetings). In the asynchronous condition, participants can engage with their group any time 24/7. In the synchronous condition, participants can engage with their group once a week at a videoconference meeting. The main questions it aims to answer are: Will participants in each condition lose about the same amount of weight? Will the participants in the asynchronous condition participate more than those in the synchronous condition? Will the participants in the asynchronous condition feel more connected to each other than those in the synchronous condition? Will the asynchronous condition cost less to deliver per pound lost than the synchronous condition? Participants will: Receive a digital weight loss program that lasts 1 year and then volunteer participants will be selected to lead the group for 1 year following the program, a phase called the "peer-led weight loss maintenance phase." Complete study assessments at baseline, 6, 12, 18, and 24 months.