No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
490 (estimated)
Sponsor
The Miriam Hospital · Other
Who this trial is looking for
This trial is looking for individuals with overweight or obesity who want to lose weight. Participants will take part in a 12-month program that helps with weight loss through different methods and support options.
Are You a Good Fit for This Trial?
You may be able to join if
I have a Body Mass Index (BMI) between 25-45.
I have daily access to the Internet at home.
You may not be able to join if
I am currently pregnant or plan to become pregnant within the next 18 months.
I have been in a weight loss program within the last 2 years.
I have a medical condition that makes exercise or dieting unsafe.
I have lost 10 pounds or more in the last 6 months.
I am currently taking weight loss medications.
I cannot walk 2 blocks without stopping.
I do not speak English.
Someone in my household is also participating in this study.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 s…
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.
Trial Locations
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City
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Status
Eligibility 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
* Prese…
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
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