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Status unknownNCT03219853Updated Nov 20, 2017

Investigating the Sensory Effects of Selenium-enriched Parsnips.

An interventional study of selenium enriched parsnips and Conventional parsnips in Food Sensory Perception and Selenium Status, sponsored by Newcastle University. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-11-20.

Sponsored by Newcastle University · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Nov 2017), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Study aims to investigate 2 topics:

  1. Flavour-Nutrient Learning (FNL) FNL proposes that personal food preferences may be influenced by unconscious mechanisms which operate to ensure the safeguarding of individual nutrient levels. The theory postulates that food preferences may change over time to address changing nutritional status (Yeomans, 2012).

    This study aims to explore FNL in humans by investigating the preferences of participants with low and high blood-selenium levels in relation to selenium-enriched parsnips. Participants will be investigated in a two-week trial in which they will undertake two food sensory tests: one before, and one after, the two-week period where they will incorporate provided parsnips into their diet.

    Some provided parsnips will contain higher levels of selenium than others, neither the participants nor the lead researcher will know which type of parsnip each participant receives.

    It is hypothesised that the second food sensory test, performed after the intervention period, will show that participants of lower initial blood-selenium levels will demonstrate an increased liking for the selenium-enriched parsnips. This may demonstrate possible FNL in humans.

  2. Relationship between selenium intake \& plasma selenium-status. This study will also examine the relationship (if any) between the selenium intake of all participants via the different types of parsnips, and their individual blood-selenium levels.

This will be assessed via blood tests before, during and after the trial in order to observe the blood-selenium levels of each participant.

It is hypothesised that the blood-selenium levels of participants of lower initial selenium readings will be the most improved upon consumption of selenium-enriched parsnips.

Read the detailed description
  1. FNL Despite a wealth of animal studies (Amanoel et al, 2016; Bach et al, 2012), human FNL research is in relative infancy.

    This study intends to investigate FNL in humans by exploring preferences of participants of different selenium-status regarding selenium-enriched parsnips, with non-enriched parsnips and other root vegetables to be used as comparators.

    Participants will be assessed by means of food sensory tests and blood analysis before, during and after the trial period.

    The trial aims to recruit 26 lower selenium-status participants of initial selenium-status approx. 70μg/L, and 26 higher selenium-status participants of initial selenium-status approx. 100μg/L (n=52). (Initial screening sample approx. n=120.) On initial screening, potential participants recording a selenium-status of under 28μg/L or over 400μg/L will be excluded (and their GP informed) for safety reasons.

    Re parsnips:

    Selenium-enriched parsnips: Se content approx. 0.30ppm. Placebo comparator: non-selenium-enriched parsnips: Se content approx. 0.06ppm. Treatment portion: 200g fresh weight per day for 14 days. Comparator vegetables: potato, celeriac, turnip.

  2. Relationship between selenium intake \& plasma selenium-status. This study will also investigate the relationship, if any, between the selenium intake of all participants via the different types of parsnips and their individual selenium status. This will be assessed via blood tests before, during and after the trial in order to observe plasma-selenium status.

This is deemed an important area for research as research suggests a trend towards selenium deficiency in the United Kingdom population (SACN, 2013). It is hoped the current study may inform the debate regarding the potential of improving United Kingdom's population selenium status via selenium-fortified foods.

02

Conditions studied

  • Food Sensory Perception
  • Selenium Status
03

In context

Lead sponsor

Newcastle University is the lead sponsor of 60 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Adults of either gender, aged over 18 years.
  2. Willingness and ability to provide blood samples, consume parsnips daily for 2 weeks, and carry out 2 sensory tests, as described in the Participant Information Sheet.
  3. Generally healthy, meaning that if health issues such as hypertension, diabetes, arthritis etc. are present, they are well controlled by appropriate treatments.

Exclusion criteria

Exclusion Criteria:

  1. Under 18 years.
  2. Difficulties with chewing or swallowing.
  3. Taste disorders.
  4. Allergies to parsnips.
  5. Impairments which may prevent mental understanding of trial, or informed consent from being given.
  6. Taking supplements providing more than 60µg Se per day
  7. Initial analysed selenium status of less than 28μg/L.
  8. Initial analysed selenium status of over 400μg/L.
  9. Any other condition that in the view of the participant's General Practitioner (GP) may make the participant unsuitable for the trial.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
52 participants (estimated)

Study arms

  • Experimental
    Lower selenium-status

    Dietary Supplement: selenium enriched parsnips · Dietary Supplement: Conventional parsnips

  • Experimental
    higher selenium

    Dietary Supplement: selenium enriched parsnips · Dietary Supplement: Conventional parsnips

Interventions

  • Dietary supplementselenium enriched parsnips

    Parsnips which have been grown in a selenium enriched environment

  • Dietary supplementConventional parsnips

    Parsnips which have been grown in a conventional environment

06

What researchers measure

Primary outcomes

  1. Food sensory perception

    change from baseline sensory perception of food samples

    Time frame: Baseline & post 14 weeks supplementation

Secondary outcomes

  1. Selenium status

    Change from baseline selenium status

    Time frame: Baseline, post 7 days supplementation ad post 14 days supplementation

07

Study locations

1 of 1 sites recruiting
  • NU-Food Research Facility
    Newcastle upon Tyne, Tyne and Wear NE17RU, United Kingdom
    Recruiting
    • Anthony W Watson, PhD · Contactanthony.watson@ncl.ac.uk · 01912083592
    • Ailsa Marsh · Principal investigator
    • Kirsten Brandt, PhD · Principal investigator
    • Nicola Brereton, PhD · Sub investigator
    • Paul Brereton, PhD · Sub investigator
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 20, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03219853
Lead sponsor
Newcastle University
Collaborators
Fera Science, Institute For Agri-food Research and Innovation
Responsible party
Sponsor
First posted
Jul 18, 2017
Start date
Mar 22, 2017
Primary completion
Dec 14, 2017 (estimated)
Completion
Dec 14, 2017 (estimated)
Last update
Nov 20, 2017

Study contacts

Ailsa Marsh
Contact
A.Marsh2@newcastle.ac.uk
0191 208 5852
Kirsten Brandt, PhD
Contact
kirsten.brandt@newcastle.ac.uk
0191 208 5852

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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