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Acute and Chronic Effects of Obesity

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 25
Maximum Age: 40
Healthy Volunteers: f
View:

• We are recruiting two groups of sedentary or untrained males and pre-menopausal females (age 25-40 years) with body mass indices (BMI) between 30.0-39.9 kg/m\^2. All participants will be required to provide a medical record and/or photographic evidence of weight at childhood (around age of 10-17 years old). Individuals with BMI between 40.0-41.9 may be included in the case that an individual with a much shorter height falls within this range, as BMI does not always properly define obesity type. Once the participant completes their DEXA scan, we will be able to more accurately assess the participant's obesity level and re-evaluate their elgibility.

Locations
Other Locations
Canada
Concordia University PERFORM Centre
RECRUITING
Montreal
Concordia University PERFORM Centre
RECRUITING
Montreal
Contact Information
Primary
Sylvia Santosa, R.D, Ph.D
s.santosa@concordia.ca
514-848-2424
Backup
Kayla Toledano, Ph.D Student
kayla.toledano@mail.concordia.ca
5145884865
Time Frame
Start Date: 2025-04-30
Estimated Completion Date: 2029-08
Participants
Target number of participants: 150
Treatments
Childhood-onset obesity
Individuals who developed severe overweight or obesity during childhood (before puberty)
Adult-onset obesity
Individuals who developed obesity as adults
Related Therapeutic Areas
Sponsors
Collaborators: Montreal Children's Hospital of the MUHC
Leads: Concordia University, Montreal

This content was sourced from clinicaltrials.gov