Energy Turnover and Appetite (NEXT)

U

University Hospital, Clermont-Ferrand

Status

Enrolling

Conditions

Obesity

Treatments

Behavioral: Low energy turnover

Study type

Interventional

Funder types

Other

Identifiers

NCT05365685
RBHP 2021 BOIRIE 2
2021-A02867-34 (Other Identifier)

Details and patient eligibility

About

The aim of the study is to compare the effect of a low versus moderate versus high energy turnover on energy intake, appetite and food reward, in adolescents with obesity. 18 adolescents with obesity will then complete three experimental sessions in a randomized order: low, high and moderate Energy turnover.

Full description

A total of 18 adolescents with obesity, aged 12-16 years olds will complete three experimental sessions in a randomized order: i) low energy turnover; ii) Moderate energy turnover and ; iii) High energy turnover. Their ad libitum energy intake at dinner will be assessed through an ad libitum buffet-type meal, their food reward assessed right before the dinner meal and their appetite sensation at regular intervals during the day.

Enrollment

18 estimated patients

Sex

All

Ages

12 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • BMI percentile > 97th percentile according to the french curves.
  • ages 12-16 years old
  • Signed consent form
  • being registered in the national social security system
  • no contraindication to physical activity

Exclusion criteria

Previous surgical interventions that is considered as non-compatible with the study.

  • Diabetes
  • weight loss during the last 6 months
  • cardiovascular disease or risks

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

18 participants in 1 patient group

adolescents with obesity
Experimental group
Description:
There is only one arm as this is an acute randomized study comparing three different conditions within the same sample of participants.
Treatment:
Behavioral: Low energy turnover

Trial contacts and locations

1

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Central trial contact

Lise Laclautre

Data sourced from clinicaltrials.gov

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