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Umbrella protocol: Non-invasive sensory and behavioural studies of eating behaviour

Umbrella protocol: Non-invasive sensory and behavioural studies of eating behaviour - Non-invasive sensory and behavioural studies of eating behaviour

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON39018
Enrollment
100
Registered
2013-10-18
Start date
2013-09-09
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

nvt nvt

Interventions

- Exposure to commercially available food products/ingredients, odours at safe concentrations. - Hunger condition (at maximum 3 hours no food/drinks that contain calories/caffeine)

Sponsors

Wageningen Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: See page 12 of the protocol. - Gender: male and/or female - Age 18-55 years old - Stable bodyweight - Healthy (as judged by the participant) - Being normosmic, i.e. having a normal olfactory sensation (optional inclusion criterium)

Exclusion criteria

Exclusion criteria: See page 12 and 13 of the protocol. - Having a taste or smell disorder - Having difficulties with swallowing/chewing - Being hypersensitive (allergy or intolerance) for the odours or tastes under study - 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 - Having a history of any medical event that could interfere with the study outcome (e.g., diabetes, gastrointestinal disease) - Having a mental or physical status that could hinder the study procedures - Being pregnant, having the intention to become pregnant or being breastfeeding - Smoking - Restraint, emotional or external eating scores may be used as additional exlusion criteria.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
NVT

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)