Synchronous vs Asynchronous Remotely Delivered Lifestyle Interventions
A Non-Inferiority Trial Comparing Synchronous and Asynchronous Remotely Delivered Lifestyle Interventions
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years to 65 Years
- Sex
- All sexes
- Healthy volunteers
- Accepted
- Compensation
- Travel or expenses covered
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Time periods mentioned: 1 year
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "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."
- Compensation
- Travel or expenses covered
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Inclusion Criteria: * BMI 27-45 * has Bluetooth or wifi connectivity at home (for scale) * goes on Facebook at least 5 days per week over the past 2 weeks * has posted/replied at least once a week in the past 2 weeks (per self-report) * has a smart phone Exclusion Criteria: * Pregnant or lactating or plans to during study period * bipolar disorder, substance abuse, psychosis, bulimia, binge eating disorder, or severe depression * had bariatric surgery or plans to during the study * currently taking meds affecting weight * lost ≥5% of weight in past 6 months * participating in another weight loss program or plans to during the study * chronic pain or medical condition that interferes with the ability to exercise * type 1 diabetes * unable to walk ¼ mile unaided without stopping * nicotine user
Study sites (1)
CT
- University of Connecticut · Storrs, CT 06269Sherry Pagoto, PhD · Study contact · 860-486-2313 · sherry.pagoto@uconn.eduSherry Pagoto, PhD · Principal investigatorMore trials in Storrs