Actively Recruiting

Age: 25Years - 40Years
All Genders
NCT07515547

Acute and Chronic Effects of Obesity

Led by Concordia University, Montreal · Updated on 2026-04-07

150

Participants Needed

2

Research Sites

222 weeks

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

The goal of this study is to understand if there are differences in the fat, muscle and metabolism of individuals who developed obesity during childhood versus those who developed obesity in adulthood. We will do this by having recruited participants undergo subcutaneous adipose tissue biopsies in the abdomen and thigh, a muscle biopsy in the thigh, collect blood and urine samples, a DEXA scan and 3 submaximal exercise tests. participants will also have their resting energy expenditure measured through indirect calorimetry to tailor a targeted weight loss protocol through caloric restriction and cardiovascular exercise (3 times a week). After 10% of weight loss is completed, study participants will repeat all tests during a 2 week weight stabilization period. At 12 weeks into the intervention, indirect calorimetry, DEXA scan and blood tests will be repeated.

CONDITIONS

Official Title

Acute and Chronic Effects of Obesity

Who Can Participate

Age: 25Years - 40Years
All Genders

Eligibility Criteria

Eligible

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
  • Provide medical record or photographic evidence of weight at childhood (around age 10 to 17 years old)
  • BMI between 40.0 and 41.9 may be included if height is very short, as BMI may not properly define obesity type
  • Weight stable for at least 2 months
  • Completion of DEXA scan for accurate obesity level assessment
Not Eligible

You will not qualify if you...

  • Pregnant or planning to become pregnant
  • Breastfeeding
  • Currently using nicotine-containing products (e.g., cigarettes, chewing tobacco, nicotine gum)
  • Taking certain antidepressants or antihypertensive medications that affect weight
  • History of surgery affecting weight or immune function (e.g., gastric bypass, magnetic implants)
  • Conditions affecting immune function or study outcomes (e.g., iron deficiency anemia)
  • Diseases such as diabetes, cancer, inflammatory bowel disease, history of eating disorders, or mental illness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

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

Loading map...

Research Team

S

Sylvia Santosa, R.D, Ph.D

CONTACT

K

Kayla Toledano, Ph.D Student

CONTACT

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here