Status:

NOT_YET_RECRUITING

Effect of Simulated Weight Loss on the Energy Cost of Locomotion in Overweight or Obese Adolescents

Lead Sponsor:

Centre Hospitalier Emile Roux

Conditions:

Obesity and Overweight

Eligibility:

All Genders

12-16 years

Phase:

NA

Brief Summary

Current literature suggests that part of the energy response to weight loss is not due to changes in fat mass and lean mass, but rather to a homeostatic adaptation aimed at limiting or even preventing...

Eligibility Criteria

Inclusion

  • Adolescents aged 12 to 16 (inclusive), at Tanner stage 3-5, with obesity defined as a body mass index (BMI) above the 97th percentile according to national growth charts.
  • No regular consumption of tobacco or alcohol,
  • No diet (no calorie restriction, no specific diet such as a normal-calorie diet enriched with protein, vegetarian, or other),
  • Adolescents affiliated with the social security system or equivalent,
  • Adolescent who has been informed and has given written consent to participate in the study,
  • Signed consent of both holders of parental authority (or one in the event of death, major incapacity, or withdrawal of parental authority).

Exclusion

  • Refusal to participate in the study,
  • Refusal of consent by parents or guardians,
  • Participation in regular and intense physical and sporting activities (no more than 150 minutes of moderate structured activity per week (according to WHO recommendations),
  • Medical or surgical history deemed by the investigator to be incompatible with the study,
  • Presence of diabetes or any other condition limiting the application of either strategy being tested,
  • Adolescents undergoing energy restriction or a weight loss program through physical activity at the time of inclusion or during the previous 6 months,
  • Taking medications that may interfere with the study results.
  • Adolescents with cardiovascular problems, i.e., subjects with a history of cardiovascular and/or neurovascular disease, as well as subjects with cardiovascular and/or neurovascular risk factors (excluding obesity/overweight).
  • Surgery in the previous 3 months,
  • Adolescents who are currently excluded from another study,
  • Pregnant or breastfeeding adolescents,
  • Adolescents under guardianship/curatorship or legal protection,
  • Parents under guardianship/curatorship or legal protection.

Key Trial Info

Start Date :

September 12 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 31 2027

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT07155746

Start Date

September 12 2025

End Date

May 31 2027

Last Update

September 19 2025

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