Actively Recruiting

Age: 11Years - 17Years
All Genders
Healthy Volunteers
NCT06391671

The Stress-obesity Axis: a Metabolomics Approach Towards Personalized Nutrition in Adolescents

Led by University Ghent · Updated on 2024-04-30

750

Participants Needed

7

Research Sites

285 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The ultimate aim of this project is to establish a validated strategy that allows for personalized intervention in adolescents (11 to 17 years) whom are assigned a state of overweight or obesity. The investigators will assess the following hypotheses: * Weight condition is reflected by the fecal metabolome (WP1) * Emotional stress is implicated in weight condition (WP1) * Functionality of the gut microbiome is related to the diet-stress-obesity axis (WP2) * Dietary pattern impacts the fecal metabolome and gut microbiome (WP2) * Personalized dietary intervention outperforms generalized dietary approaches (WP3) Participants will: * Produce a saliva, stool and hair sample * Fill in questionnaires regarding mental health, medical health and demographic information * Fill in a food frequency questionnaire and a 24-hrecalls * Be measured (height, weight, fat% and waist circumference) The samples will be analyzed using a technique called metabolomics to identify biomarker candidates with diagnostic and/or prognostic potential. Additionally, microbiome analysis will be performed to map the microbiome of all groups.

CONDITIONS

Official Title

The Stress-obesity Axis: a Metabolomics Approach Towards Personalized Nutrition in Adolescents

Who Can Participate

Age: 11Years - 17Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 11 to 17 years
Not Eligible

You will not qualify if you...

  • Overweight or obesity
  • Type 1 diabetes
  • Medical conditions including pancreatic failure
  • Developmental and hormonal disorders such as thyroid problems, adrenal problems, Kallmann's syndrome, Klinefelter's syndrome, Prader-Willi syndrome, or Congenital hypogonadotropic hypogonadism
  • Pregnancy
  • Treatment with systemic corticosteroids (e.g., cortisone, betamethasone, dexamethasone, fludrocortisone, hydrocortisone) in pill form or injections

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 7 locations

1

AZ Jan Palfijn Gent, Oost-Vlaanderen, Belgium, 9000

Ghent, Oost-Vlaanderen, Belgium, 9000

Actively Recruiting

2

Ghent University Hospital

Ghent, Oost-Vlaanderen, Belgium, 9000

Actively Recruiting

3

Clairs Vallons

Ottignies-Louvain-la-Neuve, Waals Brabant, Belgium, 1340

Actively Recruiting

4

Zeepreventorium

De Haan, West-Vlaanderen, Belgium, 8420

Actively Recruiting

5

AZ Delta

Roeselare, West-Vlaanderen, Belgium, 8800

Actively Recruiting

6

UZ Antwerpen

Antwerp, Belgium, 2000

Actively Recruiting

7

ZNA Middelheim

Antwerp, Belgium, 2000

Actively Recruiting

Loading map...

Research Team

E

Emile Callemeyn, Dr

CONTACT

L

Lynn Vanhaecke, Prof

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

The Stress-obesity Axis: a Metabolomics Approach Towards Personalized Nutrition in Adolescents | DecenTrialz