MedDiet-SN vs MedDiet-WL: Improving Weight Management and Lifestyle in Older Adults with Obesity
This study aims to compare the Mediterranean Diet with snacks (MedDiet-SN) versus the Mediterranean Diet with weight loss (MedDiet-WL) in improving physical activity, body fat, dietary intake, and adherence to the Mediterranean Diet in older adults with obesity.
Social Network Learning Program
+ Social Network Learning Program
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Treatment Study
Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.This study focuses on weight management in older adults with obesity, specifically those aged 50-79 years with a BMI of 30-50 kg/m². The main goal is to compare two dietary approaches: the Mediterranean Diet for Weight Loss (MedDiet-WL) and the Mediterranean Diet for Social Networks (MedDiet-SN). The study aims to see if participants in the MedDiet-SN group show greater improvements in bodyweight, BMI, body fat, diet quality, and physical activity compared to those in the MedDiet-WL group. The study also explores how these improvements are maintained over a year and how information about weight management is shared among participants' social networks. During the 6-month study, participants will attend 24 sessions. Their physical activity will be measured using the Godin-Shephard Leisure Time Physical Activity Questionnaire. Body fat and BMI will be assessed using a stadiometer and scale. Dietary intake will be evaluated with the Vioscreen Food Frequency Questionnaire, and adherence to the Mediterranean Diet will be measured using the Mediterranean Eating Patterns for Americans (MEPA) screener. The study also compares how participants share weight management information within their social networks and how these networks may influence the outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.532 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 50 to 79 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University of Illinois Chicago
Chicago, United StatesOpen University of Illinois Chicago in Google Maps