This protocol involves studies that aim at:1. A better understanding of sensory perception and eating behaviour2. Validation of newly developed sensory and behavioural methods3. To determine the effect of fat, sugar and/or salt reduction on sensory…
ID
Source
Brief title
Condition
- Other condition
- Appetite and general nutritional disorders
Synonym
Health condition
sensoriek en eetgedrag
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameters will depend upon the primary aim(s). For example,
sensory evaluations may be correlated to product characteristics (e.g.
instrumental analysis) and/or behavioural measures (questionnaires).
Secondary outcome
n/a
Background summary
Many studies in the field of sensory science and eating behaviour can be
considered non- or minimally invasive and of minimal risk and burden to the
participant. However, ethical approval is becoming increasingly important for
publication in peer-reviewed journals.
Study objective
This protocol involves studies that aim at:
1. A better understanding of sensory perception and eating behaviour
2. Validation of newly developed sensory and behavioural methods
3. To determine the effect of fat, sugar and/or salt reduction on sensory
perception and/or preference.
Study design
Dependent upon the primary aim(s), different tasks will be used, including
questionnaires (e.g. appetite and thirst, personality characteristics, eating
behaviour), sensory tests and/or computerized behavioural or neuropsychological
tests. Sensory tests may involve taste, odour and/or visual stimuli, or other
commercially available food products or ingredients, and may include measures
of food choice or intake. Neuropsychological tests may include questionnaires
on paper, or on computer, e.g. measuring reaction times. Computerized
behavioural experiments may involve software programs such as E-prime, CANTAB,
and other software programs (e.g. using food pictures, animation characters
that represent emotions), or saliva may be collected. Heart rate or skin
conductance can be measured. Participants may be video recorded, to assess
their facial expressions or chewing behaviour; or their eye (pupil) movements
may be tracked.
Intervention
Exposure to commercially available food products and ingredients, at
concentration levels that are approved by the Food and Consumer Product Safety
Authority (Voedsel en Waren Autoriteit), and/or odours in concentrations that
can be found in consumer products, that are non-toxic and/or can be considered
safe.
Saliva may be collected and weighed, and in a subgroup of max 50 subjects
collected saliva composition will be analysed.
Video recordings may be taken to monitor facial expressions or chewing behavior.
Pupil movements may be recorded via eye-tracking software.
Heart rate and/or skin conductance can be measured via sensors.
Hunger condition, refrain from eating/drinking food products that contain
calories and/or caffeine for a maximum of 3 hours, or to fast overnight;
Satiety condition: subjects can be given food products to consume
Study burden and risks
Each subject will spend a maximum of 60 minutes per session, with a maximum of
6 sessions. The risk associated with participation is negligible and the burden
can be considered as minimal.
Stippeneng 4
Wageningen 6708 WE
NL
Stippeneng 4
Wageningen 6708 WE
NL
Listed location countries
Age
Inclusion criteria
Aged between 18 and 55 years on the first study day
Being healthy (as judged by the subject)
Exclusion criteria
- Being an employee of the Division of Human Nutrition and Health (WU), or of
other departments involved in the study.
- Being hypersensitive (allergy or intolerance) for the odours or tastes under
study
- Having a history of any medical event that could interfere with the study
outcome (e.g. diabetes, gastrointestinal disease, thyroid disease or any other
endocrine disorder)
- Having a mental or physical status that could hinder the study procedures
- Being pregnant, having the intention to become pregnant or currently
breastfeeding, Depending on the study objective, additional exclusion criteria
may include
- Having a taste or smell disorder
- Having difficulties with swallowing/chewing
- Use of medication, except for paracetamol and contraceptive medication
- Lacking appetite
- Using an energy restricted diet during the last 2 months
- Having weight loss or weight gain of more than 5 kg during the last 2 months
- Smoking , Depending on the study objective, a screening session may be used
to determine additional exclusion criteria using scores on any of the above
described questionnaires, sensory and/or behavioural tasks.
For studies including video recordings, participants can only take part in the
study if they agree to being filmed during the experiment.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
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CCMO | NL51747.081.14 |