VertiGreens Investigating the Effects of Iron Biofortification of Microgreens on Iron Status in Women
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedFirst Submitted
Initial submission to the registry
May 6, 2025
CompletedFirst Posted
Study publicly available on registry
May 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 4, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 4, 2026
CompletedApril 30, 2026
May 1, 2025
1 year
May 6, 2025
April 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Haemoglobin status change from baseline
Iron status changes in haemoglobin
Measured at study day 1 and on study day 28
Serum iron status change from baseline
Iron status changes in serum iron
Measured at study day 1 and on study day 28
Ferritin status change from baseline
Iron status changes in ferritin
Measured at study day 1 and on study day 28
CRP change from baseline
Changes in CRP
Measured at study day 1 and on study day 28
Dietary iron intake changes compared to habitual diet
Dietary iron intake changes in iron intake compared to habitual diet measured though food diaries
every study day (28 days)
Secondary Outcomes (2)
Serum Vitamin B12 status change from baseline
Measured on study day 1 and on study day 28
Adherence to consumption of microgreens/smoothie
every study day (28 days)
Study Arms (1)
Vertigreens
EXPERIMENTALPhase 1: Habitual diet (1 week) Phase 2: Vertigreens diet: One smoothie a day containing biofortified microgreens (4 weeks)
Interventions
30g of iron biofortified microgreens consumed within a smoothie for 28 days
Eligibility Criteria
You may qualify if:
- Healthy females
- of reproductive age (18-49)
- postmenopausal (not had their period for an entire year)
You may not qualify if:
- Supplementing iron or vitamin B12
- Smoking or vaping
- Taking anticoagulant medication (blood thinners) except for Aspirin 75mg
- Anyone who is planning to be pregnant, is pregnant or breastfeeding
- Anyone with iron or vitamin B12 deficiency anaemia
- Anyone with history of anaemia in the past 3 months that required treatment
- Anyone who has Hb \<120 g/L (12 g/dL) at screening
- Anyone with food allergies to banana, mango, pineapple, coconut
- Anyone with coeliac disease
- Anyone suffering from a psychiatric disorder or any type of substance abuse
- Anyone with Type 1 diabetes and Type 2 diabetes
- Anyone suffering from unregulated thyroid disease
- Anyone with gastrointestinal conditions or bariatric surgery
- Anyone with haematological conditions including Thrombocytopaenia and Sickle cell anaemia
- Anyone with unsuitable veins for blood sampling
- +2 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rowett Institute, University of Aberdeen
Aberdeen, AB25 2ZD, United Kingdom
Study Officials
- PRINCIPAL INVESTIGATOR
Alexandra Johnstone, Prof
University of Aberdeen, Rowett Institute of Nutrition and Health
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 6, 2025
First Posted
May 15, 2025
Study Start
May 1, 2025
Primary Completion
May 4, 2026
Study Completion
May 4, 2026
Last Updated
April 30, 2026
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share