ClinicalTrials.Veeva

Menu

Experimental Overfeeding in Humans (ExpO)

University of Copenhagen logo

University of Copenhagen

Status

Completed

Conditions

Overfed
Obesity

Treatments

Other: Isocaloric diet
Other: Overfeeding diet

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The objective of this study is to determine the homeostatic mechanisms that counteract weight gain in response to experimental overfeeding.

Full description

The homeostatic regulation of body weight implies that biological processes have evolved to protect energy stores from changes to the food environment. Accordingly, many individuals remain remarkably weight stable over years without carefully considering how much they eat or how much energy they expend, which has given rise to the theory that body weight is regulated around an individual biological 'set point'. Notably, overfeeding humans in experimentally controlled conditions, support this phenomenon, but the underlying mechanisms are unknown.

To systematically map out the components of the overfed state, the investigators will execute a 2-week randomized controlled overfeeding trial in lean and overweight individuals. The trial is preceded by a 1-week lead-in period and followed by a 2-wk controlled ad libitum study period. The comparison between lean and overweight subjects, men and women, enables the determination of whether a differential response in overfeeding-induced signals is present in relation to BMI and sex.

Enrollment

24 patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female otherwise healthy subjects
  • 20-40 years of age
  • BMI (Body mass index) between 22-30 kg/m2

Exclusion criteria

  • Present or previous cardiovascular disease, diabetes or thyroid-disease
  • smoking
  • more than 3 hours of planned physical activity per week

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

Control group
Active Comparator group
Description:
Subjects in this group will have a daily energy intake equivalent of 100 % of their calculated normal daily energy intake.
Treatment:
Other: Isocaloric diet
Overfed group
Experimental group
Description:
Subjects in this group will have a daily energy intake equivalent of 150 % of their calculated normal daily energy intake.
Treatment:
Other: Overfeeding diet

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems