Comparing online and group-based programs for weight loss
Comparison of Behaviorally-Based Remote Approaches to Optimize Weight Loss and Identification of Factors Which Characterize Treatment Response
NA · The Miriam Hospital · NCT06875622
This study is testing whether an online weight loss program works better than a group video program for helping people lose weight and stay engaged over a year.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 490 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | The Miriam Hospital (other) |
| Locations | 1 site (Providence, Rhode Island) |
| Trial ID | NCT06875622 on ClinicalTrials.gov |
What this trial studies
This trial aims to compare two different formats for delivering a 12-month behavioral weight loss program: an automated online program and a group-based videoconference program. Participants will be randomized into one of four groups, receiving either coaching or no coaching alongside their chosen format. The study will assess weight loss outcomes and participant engagement at multiple time points, including baseline, 6 months, 12 months, and 18 months post-treatment. Additionally, the research seeks to identify which intervention combinations are most effective for different individuals, potentially leading to tailored recommendations for future weight loss programs.
Who should consider this trial
Good fit: Ideal candidates are individuals with a Body Mass Index between 25-45 kg/m2 who have daily access to the internet.
Not a fit: Patients who are currently pregnant, have a recent history of significant weight loss, or have contraindicated medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective weight loss strategies that are accessible and tailored to individual needs.
How similar studies have performed: Other studies have shown promise in using remote interventions for weight loss, indicating that this approach is both relevant and potentially effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Body Mass Index between 25-45 kg/m2 * Daily, home Internet access Exclusion Criteria: * Currently pregnant, planning to become pregnant within the next 18 months, or pregnant within the past 6 months * Current or recent enrollment (\<2 years) in a weight loss program * Presence of any medical condition for which exercise, weight loss, or dietary restriction is contraindicated * Recent weight loss (≥10 pounds within the past 6 months) * Currently taking weight loss medications or history of bariatric surgery * Inability to walk 2 blocks without stopping * Non-English speaking * A member of one's household is participating in the study * History of anorexia or bulimia nervosa
Where this trial is running
Providence, Rhode Island
- The Miriam Hospital's Weight Control and Diabetes Research Center — Providence, Rhode Island, United States (RECRUITING)
Study contacts
- Study coordinator: Jessica L Unick, PhD
- Email: junick@brownhealth.org
- Phone: 401-793-8966
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Obesity/therapy, behavioral weight loss, remote interventions, diet and exercise