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Virtual Weight Management Program for Obesity
Study Summary
This trial will expand a virtual weight loss program to rural areas in Illinois, using dietary and lifestyle modifications to help adults with obesity. Rural areas face unique challenges with obesity.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I have a working email address.I am either younger than 18 or older than 75.I have not been able to weigh myself every day.I am willing to lose 20 lb. or more and keep it off for a year.My BMI is in the underweight to normal range.I have had or am planning to have weight loss surgery within a year.I am between 18 and 75 years old.I will weigh myself daily for two years.
- Group 1: Weight Management Intervention
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Is this research program recruiting geriatric individuals?
"As per the study's criteria, potential participants must be of age 18 or older but not exceed 75 years old."
Is this research effort currently accepting participants?
"Clinicaltrials.gov lists this medical trial as currently closed to new participants - it was posted on May 9th 2022 and revised lastly on October 19th 2022. Despite this, there are 1283 other clinical trials that are presently recruiting patients across the country."
Are there still open spots available to me in this investigation?
"The prerequisites for this clinical trial necessitate that applicants are of the ages between 18 and 75, with obesity. Approximately 16 patients will be accepted."
Who else is applying?
What site did they apply to?
What portion of applicants met pre-screening criteria?
Why did patients apply to this trial?
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