Clinical Trials Directory

Trials / Completed

CompletedNCT05897411

Deconditioning of Acquired Food Aversion

Factors That Determine the Responses to Meal Ingestion: Deconditioning of Acquired Food Aversion

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Hospital Universitari Vall d'Hebron Research Institute · Academic / Other
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

Background. Aversive conditioning impairs the rewarding value of a comfort meal. Our aim is to demonstrate the potential effect of deconditioning to reverse aversive conditioning and restore the hedonic postprandial response. Methods: A sham-controlled, randomised, parallel, single-blind study will be performed on 12 healthy women (6 per group). The rewarding value of a comfort meal will be measured at initial exposure, after aversive conditioning (masked administration of the same meal with a high-fat content) and after a deconditioning intervention (unmasking the aversive conditioning paradigm in the deconditioning group vs sham intervention in the control group). Digestive well-being (primary outcome) will be measured every 10 min before and 60 min after ingestion using graded scales. The effect of deconditioning (change from aversive conditioning to deconditioning) will be compared to sham deconditioning in the control group. Expected results: The comfort meal at first exposure will induce a pleasant postprandial experience, which will be impaired by aversive conditioning; this effect will be reverted by deconditioning and the hedonic value of the comfort meal will be restored.

Conditions

Interventions

TypeNameDescription
BEHAVIORALUnmasking previous conditioning procedureAn explanation of the method for aversive conditioning of the comfort meal (masked administration of the meal with a high fat supplement) will be provided.
BEHAVIORALNo unmasking of previous conditioningAn explanation of the method for aversive conditioning of the comfort meal (masked administration of the meal with a high fat supplement) will not be provided.

Timeline

Start date
2023-01-10
Primary completion
2023-05-15
Completion
2023-05-31
First posted
2023-06-09
Last updated
2023-06-09

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05897411. Inclusion in this directory is not an endorsement.