Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06875622

Remote Approaches for Optimizing Weight Loss (Elevate Weight Loss Trial)

Led by The Miriam Hospital · Updated on 2025-03-18

490

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

Sponsors

T

The Miriam Hospital

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Remote Approaches for Optimizing Weight Loss (Elevate Weight Loss Trial)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Body Mass Index between 25-45 kg/m2
  • Daily, home Internet access
Not Eligible

You will not qualify if you...

  • Currently pregnant, planning to become pregnant within the next 18 months, or pregnant within the past 6 months
  • Current or recent enrollment (less than 2 years) in a weight loss program
  • Medical condition that makes exercise, weight loss, or diet restrictions unsafe
  • Recent weight loss of 10 pounds or more within the past 6 months
  • Currently taking weight loss medications or history of bariatric surgery
  • Unable to walk 2 blocks without stopping
  • Non-English speaking
  • A member of your household is participating in the study
  • History of anorexia or bulimia nervosa

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Miriam Hospital's Weight Control and Diabetes Research Center

Providence, Rhode Island, United States, 02903

Actively Recruiting

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Research Team

J

Jessica L Unick, PhD

CONTACT

J

Jennifer Webster

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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