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Validation of a French-version of the Leeds Food Preference Questionnaire in Normal Weight and Patients With Obesity

Validation of a French-version of the Leeds Food Preference Questionnaire in Normal Weight and Patients With Obesity

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04041830
Acronym
LFPQ-F
Enrollment
37
Registered
2019-08-01
Start date
2019-12-08
Completion date
2021-06-25
Last updated
2022-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Normal Weight Adults, Adults With Obesity

Keywords

Appetite, Food Reward, Methodological approach

Brief summary

While Food reward is an important component of the appetite control to consider, there is actually no tool that has been developed in French to perform its evaluation. The Leeds Food Preference Questionnaire (LFPQ) is a validated and recognized tool to assess food reward, being however developed for British populations. The aim of this work is to validate a French version of the LFPQ among lean and obese adults.

Detailed description

50 lean and 50 patients with obesity between 20 and 55 years old (50% women and 50% men), will be recruited. After an evaluation of their body composition by impedance meter, and of their dietary status by questionnaires (TFEQ/DEBQ), they will be asked to perform twice the same experimental sessions. They will be asked during this session to arrive at 08:00 am after a 12-hour fast and will receive a calibrated breakfast. Before and after a lunch calibrated meal, they will be asked to perform the French version of the computerized questionnaire LFPQ. Appetite feelings will be assessed at regular intervals.

Interventions

BEHAVIORALVisit 1

the participants will fill in the LFPQ questionnaire before and after a lunch test meal

BEHAVIORALVisit 2

this is a replication of Visit 1, testing the reproducibility of the LFPQ and of its response to a meal.

Sponsors

Appetite Control and Energy Balance Research Group, UNiversity of Leeds, Leeds, UK
CollaboratorUNKNOWN
Laboratoire AME2P. Campus universitaire des cezeaux, 63170 Aubiere, Cedex
CollaboratorUNKNOWN
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI between 30 and 38 kg.m² for the obese patients and 20 and 25 for the lean ones. * registered to the national social security system * Signed consent

Exclusion criteria

* eating disorders * metabolic disease such as hypertension and Type 2 diabetes

Design outcomes

Primary

MeasureTime frameDescription
Change in Food rewardday 1 , day 8The participants will be asked to complete the developed French version of the computer-based procedure to measure food reward (Leeds Food Preference Questionnaire; LFPQ) (Finlayson, King et al. 2008).

Secondary

MeasureTime frameDescription
Body fat and fat free massday 0the percentage of body fat free and the quantity of fat free mass will be assessed using Bio-impedance (BIA)
Dietary statusday 0the level of dietary restriction/disinhibition will be assessed using the TFEQ questionnaire.
Body fat massday 0the percentage of body fat and the quantity of fat mass will be assessed using Bio-impedance (BIA)
Hungerday 1, day 1 + 30minutes, day 1+60minutes, day 1+ 90minutes , day 8, day 8 + 30minutes, day 8+60minutes, day 8+ 90minutesthe hunger sensation will be assessed using visual analogue scales of 150 mm.
desire to eatday 1, day 1 + 30minutes, day 1+60minutes, day 1+ 90minutes , day 8, day 8 + 30minutes, day 8+60minutes, day 8+ 90minutesthe desire to eat sensation will be assessed using visual analogue scales of 150 mm.
Prospective Food consumptionday 1, day 1 + 30minutes, day 1+60minutes, day 1+ 90minutes , day 8, day 8 + 30minutes, day 8+60minutes, day 8+ 90minutesthe Prospective Food consumption sensation will be assessed using visual analogue scales of 150 mm.
Satietydday 1, day 1 + 30minutes, day 1+60minutes, day 1+ 90minutes , day 8, day 8 + 30minutes, day 8+60minutes, day 8+ 90minutesthe Satiety sensation will be assessed using visual analogue scales of 150 mm.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026