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Innovative Food Structures to Enhance Nutrient Bioavailability

Innovative Food Structures to Enhance the Sensory Experience, the Nutrient Profile and Nutrient Bioavailability for Older People

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04156074
Acronym
NutriPlus
Enrollment
80
Registered
2019-11-07
Start date
2019-11-04
Completion date
2021-12-31
Last updated
2023-03-06

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

Conditions

Aging Well, Vitamin D Deficiency

Keywords

Vitamin D, Bioavailability, Aging, Fortified foods, Vitamin D status, 25-hydroxyvitamin D

Brief summary

This randomized controlled trial (RCT) will compare the change in vitamin D status (25-hydroxyvitamin D nmol/L) after a 4 week intervention with 4 groups: 1. Vitamin D enriched (20ug) olive oil emulsion drink 2. Vitamin D enriched (20ug) coconut oil emulsion drink 3. Placebo emulsion drink 4. Vitamin D supplement (20ug) Participants will be randomized to 1 of 4 intervention group. Hypothesis 1: 25-hydroxyvitamin D concentrations are higher in the olive oil emulsion drink group compared to the placebo emulsion drink group post intervention. Hypothesis 2: 25-hydroxyvitamin D concentrations are higher in the olive oil emulsion drink group compared to the coconut oil emulsion drink group post intervention.

Interventions

DIETARY_SUPPLEMENTVitamin D enriched (20 mcg/day) olive oil emulsion drink

Vitamin D enriched (20 mcg/day) olive oil emulsion drink. 30 mL drink daily

DIETARY_SUPPLEMENTVitamin D enriched (20 mcg/day) coconut oil emulsion drink

Vitamin D enriched (20 mcg/day) coconut oil emulsion drink 30 mL drink daily

DIETARY_SUPPLEMENTPlacebo coconut oil emulsion drink

Placebo coconut oil emulsion drink 30 mL drink daily

DIETARY_SUPPLEMENTVitamin D supplement (20 mcg/day)

Vitamin D supplement (20 mcg/day) Pill consumed daily

Sponsors

Department of Agriculture Food and the Marine
CollaboratorUNKNOWN
University College Dublin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Masking description

Double Blind

Intervention model description

Parallel Randomized Controlled Trial

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

• Healthy adults

Exclusion criteria

* Pregnant/lactating * Smokers * Individuals who are not free-living * An inability to read, write or understand English * Following a strict diet for any reason, insulin dependent diabetes, coeliac etc. * Disease that requires chronic therapeutic nutritional or medical treatment * Those with conditions that may affect kidney function * Those with osteoporosis * Those taking supplemental vitamin D * Those who have been on a sun holiday in the last 2 months * Those with a milk protein allergy or lactose intolerance

Design outcomes

Primary

MeasureTime frameDescription
Vitamin D statusBaseline to 28 daysChange in vitamin D status measured as serum 25-hydroxyvitamin D (nmol/L)

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026