Synchronous vs Asynchronous Remotely Delivered Lifestyle Interventions - Trial NCT06393725
Access comprehensive clinical trial information for NCT06393725 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Connecticut and is currently Not yet recruiting. The study focuses on Obesity. Target enrollment is 328 participants.
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Study Focus
Sponsor & Location
University of Connecticut
Timeline & Enrollment
N/A
Jun 01, 2024
Jun 30, 2028
Primary Outcome
Weight,Weight
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 we call the peer-led
 weight loss maintenance phase. Complete study assessments at baseline, 6, 12, 18, and 24
 months.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06393725
Non-Device Trial