Actively Recruiting
Acute and Chronic Effects of Obesity Study Evaluating Differences in Fat, Muscle, and Metabolism Based on Childhood or Adult Obesity Onset
Led by Concordia University, Montreal · Updated on 2026-04-07
150
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Concordia University, Montreal
Lead Sponsor
M
Montreal Children's Hospital of the MUHC
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating differences in fat, muscle, and metabolism between individuals who developed obesity during childhood and those who developed it in adulthood. The study focuses on people aged 25 to 40 with obesity to better understand how the timing of obesity onset affects body composition and metabolic health. This observational study aims to explore specific immune, muscle, and fat tissue characteristics and blood inflammatory markers over several years. Participants will undergo various tests including biopsies of abdominal and thigh fat and thigh muscle, blood and urine collection, DEXA scans, and submaximal exercise tests. Resting energy expenditure will be measured using indirect calorimetry to design a personalized weight loss plan involving calorie restriction and cardiovascular exercise three times a week. Once participants lose about 10% of their starting body weight, all tests will be repeated during a two-week weight stabilization phase. After 12 weeks, indirect calorimetry, DEXA scans, and blood tests will be repeated again to assess changes. Throughout the study, participants will be monitored closely with repeated assessments to measure immune cell counts, fat cell characteristics, muscle and fat tissue interaction, and blood markers of inflammation. The study includes a focus on weight stabilization and maintaining the weight loss to understand lasting effects. The total follow-up involves repeated evaluations over several years to capture both acute and chronic effects of obesity based on its onset timing.
CONDITIONS
Brief Title
Acute and Chronic Effects of Obesity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Sedentary or untrained males and pre-menopausal females aged 25 to 40 years
- Body mass index (BMI) between 30.0 and 39.9 kg/m2, or 40.0 to 41.9 for shorter individuals
- Medical record or photographic evidence of weight during childhood (ages 10-17)
- Weight stable for at least 2 months
- Willingness to participate in tests including biopsies, scans, blood and urine collection, and exercise sessions
You will not qualify if you...
- Pregnant, planning pregnancy, or breastfeeding
- Currently using nicotine products like cigarettes or chewing tobacco
- Taking certain antidepressants or anti-hypertensive medications
- History of surgery such as gastric bypass or magnetic implants
- Conditions or diseases affecting immune function or study outcomes, including diabetes, cancer, inflammatory bowel disease, iron deficiency anemia, eating disorders, or mental illness
- Unable to participate due to health or medical reasons
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Duration not specified
Participants follow a conventional weight loss program to lose approximately 10% of their starting body weight.
Duration - Up to 5 years
Participants are monitored over multiple years to evaluate immune cell levels, fat and muscle characteristics, and blood inflammatory markers.
Trial Site Locations
Total: 2 locations
1
Concordia University PERFORM Centre
Montreal, Quebec, Canada, H4B 1R6
Actively Recruiting
2
Concordia University PERFORM Centre
Montreal, Quebec, Canada
Actively Recruiting
Research Team
S
Sylvia Santosa, R.D, Ph.D
K
Kayla Toledano, Ph.D Student
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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