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VertiGreens Investigating the Effects of Iron Biofortification of Microgreens on Iron Status in Women

VertiGreens Investigating the Effects of Iron Biofortification of Microgreens on Iron Status in Women

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06972927
Enrollment
30
Registered
2025-05-15
Start date
2025-07-18
Completion date
2026-05-04
Last updated
2026-08-20

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

Conditions

Iron Biomarkers/Status

Keywords

vertical farming, iron biomarkers, iron status, biofortification, microgreens

Brief summary

The investigators present a pilot diet intervention study, to be conducted as a within-subject design, to assess the feasibility of iron biofortified microgreens on iron intake and status in women of reproductive age and postmenopausal women. This will be investigated by providing smoothie kits for 28 days containing these microgreens and determining the impact on iron biomarkers. The investigators will also assess habitual diet, BMI, physical activity and gastrointestinal symptoms. This study will be a proof-of-concept exploratory study to explore diet based biofortification through vertical farming systems.

Detailed description

In this study microgreens that were grown using agronomic iron biofortification will be supplied to women to add to their diet to establish the potential nutritional impact of iron biofortified microgreens on overall iron intake and iron status. Furthermore, it will assess the adherence to the provided consumption recommendations of the biofortified crops.

Interventions

OTHERSmoothie containing iron biofortified microgreens

30g of iron biofortified microgreens consumed within a smoothie for 28 days

Sponsors

University of Aberdeen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy females * 15 of reproductive age (18-49) * 15 postmenopausal (not had their period for an entire year)

Exclusion criteria

Medication

Design outcomes

Primary

MeasureTime frameDescription
Haemoglobin status change from baselineMeasured at study day 1 and on study day 28Iron status changes in haemoglobin
Dietary iron intake changes compared to habitual dietevery study day (28 days)Dietary iron intake changes in iron intake compared to habitual diet measured though food diaries
Ferritin status change from baselineMeasured at study day 1 and on study day 28Iron status changes in ferritin
CRP change from baselineMeasured at study day 1 and on study day 28Changes in CRP
Serum iron status change from baselineMeasured at study day 1 and on study day 28Iron status changes in serum iron

Secondary

MeasureTime frameDescription
Serum Vitamin B12 status change from baselineMeasured on study day 1 and on study day 28Vitamin B12 status changes
Adherence to consumption of microgreens/smoothieevery study day (28 days)intake measured through food diaries

Countries

United Kingdom

Contacts

PRINCIPAL_INVESTIGATORAlexandra Johnstone, Prof

University of Aberdeen, Rowett Institute of Nutrition and Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026