The primary objectives of the current study are to determine the influence of unaware and passively smelled macronutrient-related odours on appetite, and actual food intake, in normal weight and unrestrained individuals.The secondary objectives of…
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Brief title
Condition
- Other condition
Synonym
Health condition
eetgedrag
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameters are: change in specific appetite for foods congruent
vs incongruent with the exposed odour (difference between pre and post odour
exposure), and food intake (for congruent vs incongruent foods).
Secondary outcome
Secondary parameters are: food/macronutrient preference (relative preference
score), and correlation between self-reported macronutrient preference and
actual macronutrient intake.
In addition, influences of hunger and satiety states on psychometric
performance will be explored.
Background summary
Living in an obesogenic environment, we are surrounded by food odour cues that
trigger these unconscious decisions and induce us to (over)eat. Olfaction plays
an important role in eating behaviour by detecting foods, attracting our
attention, and triggering our appetite. However, the effect of food odours on
subsequent behavioural responses remains unclear.
Olfaction may play a role in appetite and meal initiation. Some studies have
suggested that food odours increases appetite for foods with similar
properties, sensory-specific appetite, and may generalize across foods within
certain categories as taste and energy-density.
On the other hand, contradictory findings have been reported between the
influence of odours on appetite versus actual food choice and intake.
Differences in intensity, type of exposure (explicit or implicit), and
awareness of the odour cue could be responsible for the lack of consistency in
these findings.
Therefore, we propose a series of behavioural studies to extend the knowledge
in the (macronutrient signalling) function of odours and its impact on appetite
and actual food intake. We aim to disentangle the differential effects of
intensity, exposure method (explicit and implicit), and awareness of the cue:
Aware and actively smelling of odours (part A; NL66580.081.18) and unaware
smelling by means of ambient odours (part B).
Results of part A showed that food odours influence SSA but did not affect food
intake. The knowledge learned from part A was used to establish the methods in
the current protocol (part B).
Study objective
The primary objectives of the current study are to determine the influence of
unaware and passively smelled macronutrient-related odours on appetite, and
actual food intake, in normal weight and unrestrained individuals.
The secondary objectives of the current study are to determine the influence of
unaware and passively smelled macronutrient-related odours on food preferences.
Also, we will determine the correlation between self-reported macronutrient
preference and actual macronutrient intake.
Cover story for participants: The influence of hunger and satiety on abilities
of logic reasoning. Participants will be debriefed at the end of the last test
session.
Study design
The current study is a counter-balanced cross-over intervention study.
Subjects will take part in an information meeting and four test sessions. In
each test session, subjects will be exposed to one of the four conditions
(odour representing food high in carbohydrates, protein and fat, and low in
calories) and tested for behavioural measures. In each test session, subjects
will be asked to rate their general and specific appetite and stress, to
perform a computer-based task on food preferences (MTPRT), and some
psychometric tasks (to assess logical reasoning ability; this is done to
distract subjects from the actual goal of the study). Participants will be
provided with lunch to covertly measure ad libitum food intake.
Intervention
In each test session, participants will be exposed to one of the four
conditions (odour representing food high in carbohydrates, protein and fat, and
low in calories) for a few minutes.
Study burden and risks
This study is non-therapeutic. The risk associated with participation is
negligible. The burden can be considered as low. The study includes five site
visits in a non-satiated state and an information meeting (approx. total
duration of 5 hours). All odours and food products are considered safe to
use/consume and commercially available. The level of the questionnaires to
measure your ability to reason logically is average to difficult.
Stippeneng 4
Wageningen 6708 WE
NL
Stippeneng 4
Wageningen 6708 WE
NL
Listed location countries
Age
Inclusion criteria
Dutch women.
Healthy and normal body weight (BMI: 18.5 - 25 kg/m^2).
Between 18 * 35 years old.
Normal sense of smell.
Normal sense of taste and colour blindness will be assessed during the
screening session. However, the goal of these tasks are to distract the
attention from the odour identification test. Therefore, these tasks are not
considered as inclusion criteria for the real aim of the study They will be
added in the files for participants information (E1/E2, E3, F1-PIF) in order to
be consistent with our alternative goal .
In the last test session, participants will be performed a debriefing
questionnaire on aim of the study and awareness of any odour. After subjects
complete the questionnaire, they will be briefed about the actual aim of the
study by the researchers. Subjects are welcomed to ask any further question.
Exclusion criteria
Restrained eaters.
Habitual smokers.
Any food restriction such as vegetarian, vegan, etc.
Any allergy, intolerance or oversensitivity to food used in this study.
Dislike of the food products used in the study (Liking <40 mm VAS).
Use of medication other than paracetamol and hormonal contraceptives.
Pregnant/have the intention to become pregnant during the experiment/are
currently breastfeeding.
Reported weight loss or weight gain of more than 5 kg or following a special
diet in the two months prior the study.
Staff member of the Division of Human Nutrition and Health at Wageningen
University, or students currently performing a MSc thesis at the Division.
Participation in other medical studies.
Previously participated in STER study 1
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
In other registers
Register | ID |
---|---|
CCMO | NL69840.081.19 |
Other | NL7742 |
OMON | NL-OMON22413 |