NCT06875622Recruiting
Remote Approaches for Optimizing Weight Loss (Elevate Weight Loss Trial)
Comparison of Behaviorally-Based Remote Approaches to Optimize Weight Loss and Identification of Factors Which Characterize Treatment Response
Source: ClinicalTrials.gov · Last updated 29 Oct 2026
Brief summary (registry, in English)
The purpose of this trial is to compare two delivery formats for weight loss (automated online program vs. group-based videoconference program) and to examine the added effect of individual coaching (vs. no coaching) for individuals with overweight or obesity. All participants enrolled in this study will receive a 12-month behavioral weight loss program (varying in delivery format and individual support), and will be provided with weight loss, calorie intake, and exercise goals. Assessments will occur at baseline, 6 (mid-treatment), 12 (post-treatment), and 18 months (following 6 months of no intervention). We will also seek to determine which combination of intervention approaches works best for whom and develop algorithms which can be used to refer patients into remote programs in clinical settings or future trials.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 490 (estimated)
- First submitted
- 8 Mar 2025
- Start date
- 3 Mar 2025
- Primary completion date
- 27 Apr 2028
- Lead sponsor
- The Miriam Hospital
- Diseases
- Obesity
- NCT number
- NCT06875622
What you commit to
- Study type: Interventional
- Planned participants: 490
- From 3 Mar 2025 to the primary completion date, 27 Apr 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Currently taking weight loss medications or history of bariatric surgery
Other illness
- Presence of any medical condition for which exercise, weight loss, or dietary restriction is contraindicated
- History of anorexia or bulimia nervosa
Age
- Current or recent enrollment (\<2 years) in a weight loss program
Other
- Currently pregnant, planning to become pregnant within the next 18 months, or pregnant within the past 6 months
- Recent weight loss (≥10 pounds within the past 6 months)
- Inability to walk 2 blocks without stopping
- Non-English speaking
- A member of one's household is participating in the study
Who the study is looking for
- Body Mass Index between 25-45 kg/m2
- Daily, home Internet access
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The Miriam Hospital's Weight Control and Diabetes Research Center Coordinator of this site? Confirm its status | Providence | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.