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NASIC

NASIC: Neural Activation of Social Influence and Colours

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20259
Enrollment
27
Registered
2016-06-15
Start date
2016-09-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Social influence Colour Associations Popularity Taste Choice Healthiness Attractiveness

Interventions

fMRI experiment where participants see and taste supermarket products

Sponsors

Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO grant number: 057-13-001)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age: 18 - 30 years old • BMI: 18.5 – 27 kg/m2 • Healthy (as judged by the participant) • Being right handed • Users of the used product categories (e.g. dairy drinks) at least 5 consumption occurrences a year. • Willing to comply with the study procedures • Willing to be informed about incidental findings of pathology

Exclusion criteria

Exclusion criteria: • Colour-blind • Having difficulties with tasting, smelling, swallowing or eating • Weight loss or weight gain of 5 kg or more during two months (preceding the screening session) • Stomach or bowel diseases • Diabetes, thyroid disease, kidney disease and other chronical disorders • Having epilepsy or other neurological disorders • Having claustrophobia, schizophrenia or another mental illness • Usage of daily medication other than oral contraceptives, paracetamol or H1-antihistaminergic drugs • Pregnancy during the last 6 months, having the intention to become pregnant or lactating • Smoking on average more than one cigarette/cigar a day • Being allergic/intolerant for products under study • Working or doing an internship/thesis at the Department of Human Nutrition (WUR) • Working or doing an internship/thesis at the Department of Marketing and Consumer Behaviour (WUR) • Current participation in other (medical) research (except the EetMeetWeet study) • Having a history of or current alcohol consumption of on average more than 21 units per week • Having objections against being informed about incidental findings of pathology and against the general physician being informed about incidental findings of pathology (see F1 Inclusion questionnaire) • Having a contra-indication to MRI scanning (including, but not limited to): • Pacemakers and defibrillators • Intraorbital or intraocular metallic fragments • Ferromagnetic implants • Presence of non-removable metal objects in the mouth • Presence of non-removable piercings

Design outcomes

Primary

MeasureTime frame
Experimental task 1: Social influences The main study parameter is the difference in brain activation when (1) evaluating packages containing information on popularity or not, and (2) when indicating purchase intention between conditions. Experimental task 2: Colour cue The main study parameter is the difference in brain activation when evaluating packages containing different colours (signalling healthiness or attractiveness) combined with tasting.

Secondary

MeasureTime frame
Secondary parameters Social influences The secondary study parameter is to assess the use of (brain) activity coefficients as mediators in choice prediction model. Secondary parameters Colour cue The secondary study parameter is the difference in brain activation when evaluating packages containing different colours (signalling healthiness or attractiveness) without tasting. We are also interested in the difference in brain activation when evaluating our commercially available dairy drink, or enhanced/diluted dairy drink.

Contacts

Public ContactIrene Tijssen

Afdeling Humane Voeding, Wageningen University

E-mail: Irene.tijssen@wur.nl/E-mail: nasik@wur.nlTelefoon: 0317-485979

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)