Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT06972927

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

Led by University of Aberdeen · Updated on 2026-04-30

30

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators present a diet intervention study, to be conducted as a within-subject design, to assess the effect of the provision 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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy females
  • Women of reproductive age between 18 and 49 years old
  • Postmenopausal women who have not had their period for at least one year
Not Eligible

You will not qualify if you...

  • Currently supplementing with iron or vitamin B12
  • Smoking or vaping
  • Taking anticoagulant medication except Aspirin 75mg
  • Planning pregnancy, pregnant, or breastfeeding
  • Iron or vitamin B12 deficiency anemia
  • History of anemia in past 3 months requiring treatment
  • Hemoglobin less than 120 g/L at screening
  • Food allergies to banana, mango, pineapple, or coconut
  • Coeliac disease
  • Psychiatric disorders or substance abuse
  • Type 1 or Type 2 diabetes
  • Unregulated thyroid disease
  • Gastrointestinal conditions or past bariatric surgery
  • Hematological conditions including thrombocytopenia and sickle cell anemia
  • Unsuitable veins for blood sampling
  • Blood donation within last 16 weeks
  • Unable to fluently speak, read, and understand English

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Rowett Institute, University of Aberdeen

Aberdeen, United Kingdom, AB25 2ZD

Actively Recruiting

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Research Team

A

Alexandra Johnstone, Prof

CONTACT

A

Annika Bucky

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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