Skip to main content
OpenTrials
Completed

NCT Number: NCT07481240

A Household-Based Dietary Intervention Study of Vitamin D Fortified Bread in Irish Families

Vitamin D deficiency is common. It is caused by limited sun availability together with a low supply of vitamin D in the food system. There is a high prevalence of low vitamin D status around the world. In Ireland, our relatively northern latitude and prevailing weather mean that UVB availability for skin synthesis of vitamin D is limited in this country and our population relies on the dietary supply of vitamin D to prevent deficiency. Thus, the endemic Irish problem of vitamin D malnutrition is due to the lack of vitamin D in our food system. Dietary guidelines cannot address this issue because foods naturally rich in vitamin D are very few and infrequently consumed.

The FamDBread study will test the hypothesis that a vitamin D-fortified bread as part of a healthy diet that includes vitamin D-fortified foods is effective in preventing low vitamin D status during winter, and safe for families to consume.

Completed

Looking for future studies?

Notify Me

Key information

Age range

5 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Human Nutrition Studies Unit, School of Food and Nutritional Sciences, Cork, Co. Cork, Ireland

Loading trial locations.

About this study

This randomised controlled dietary intervention study aims to recruit households/families of children, teens and adults, with 128 participants who will be randomised to receive vitamin D-fortified bread and advice to consume additional commercially available fortified foods (Treatment group) or identical unfortified bread and advice to consume additional commercially available fortified foods (Control group). The outcome of the study is to test whether increasing vitamin D intake through food (Treatment group) is sufficient to prevent wintertime vitamin D deficiency (measured using serum concentrations of 25-hydroxyvitamin D <30 nmol/L) in comparison with the Control group.

The target vitamin D intake for the treatment group in this study is >20 μg/ day vitamin D. This will maintain serum concentrations of 25-hydroxyvitamin D (25(OH)D) (the biomarker of vitamin D status) > 30 nmol/L, the clinical deficiency threshold to prevent metabolic bone disease, in over 90% of participants. At this vitamin D intake level, about 80% of participants will have a 25(OH)D concentration > 50 nmol/L, the personal intake target in the US and EU.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provide written informed consent if over 16 years; informed parental consent for children under-16 years, plus age-appropriate assent for children under-16 years.
  • Be a household with at least one adult ≥18 years, with at least one dependent aged 5 years or older.
  • Willing to consume bread provided and have storage capacity for frozen bread.
  • Be in good general health.
  • Be willing to follow the assigned diet for 8 weeks and attend the required appointments.

Exclusion criteria

  • Daily consumption of a vitamin D supplement with a dose exceeding >10µg/d (400 IU) equivalent.
  • Exposure to factors that may influence vitamin D status, such as winter sun holiday, ski holiday, tanning beds etc.
  • Are following a medically prescribed diet.
  • Have a diagnosis of a medical condition that may interfere with vitamin D absorption, such as Coeliac disease, Inflammatory Bowel Disease, cystic fibrosis, or metabolism, such as liver disease, renal disease.
  • Have a history of active cancer or a diagnosis of cancer within the past 5 years.
  • Have an allergy to the bread ingredients.
  • Are participating in another research study with an intervention or other lifestyle programme that would interfere with the outcomes of the study.
  • Are unable to read, write, or understand English.

Treatment and study plan

Fortified Bread

Other

Intervention group will be supplied with fortified bread delivering >20 μg vitamin D3 in a daily portion and will receive dietary advice to incorporate fortified foods that are commonly available on the market in their diet.

Unfortified bread

Other

Placebo control group will be supplied with unfortified bread and will receive dietary advice to incorporate fortified foods that are commonly available on the market in their diet.

Primary outcomes

  1. Serum concentrations of 25-hydroxyvitamin D (25(OH)D)

    Time frame: 8 weeks

    Comparison of the number of participants with low vitamin D status (e.g. <30 nmol/L and < 50 nmol/L serum 25(OH)D) between treatment and placebo groups

Secondary outcomes

  1. Vitamin D intakes

    Time frame: 8 weeks

    Comparison of prevalence of inadequate vitamin D intakes relative to North American and European dietary recommendations

  2. Serum concentrations of albumin-corrected serum calcium concentrations as a safety measure

    Time frame: 8 weeks

    Comparison of albumin-corrected serum calcium concentrations < 2.6 mmol/L between treatment and placebo control groups

  3. Circulating biomarkers of metabolic health status

    Time frame: 8 weeks

    Comparison of circulating biomarkers of metabolic health status and metabolomic markers between active and placebo groups

Sponsors and collaborators

Lead sponsor

University College Cork

Other

Collaborators

  • University College Dublin

Registry information

Official study title

Fam-D-Bread: A Household-Based Dietary Intervention Study of Vitamin D Fortified Bread in Irish Families

Acronym: Fam-D-Bread

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 18, 2026
Registry last updated
May 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.