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NCT Number: NCT07312435

B-vitamins and Omega-3 Fatty Acids and Biomarkers of Brain Atrophy.

A poor nutrition status is a modifiable risk factor for cognitive decline and dementia. In particular, evidence links low status of certain B-vitamins and ω-3 fatty acids (ω-3 FA) with a greater risk of cognitive decline and dementia. Although these dietary components are typically investigated separately, post-hoc analyses of existing clinical trial data and experimental work indicate that B-vitamins and ω-3 FA may exert synergistic beneficial effects on processes related to brain health and cognition. However, this combination has not been tested directly in humans. In the proposed BOOMERANG project, we will study the effects of jointly supplementing with B-vitamins and a highly bioavailable ω-3 FA supplement, Lysoveta, on a robust biomarker of brain atrophy, the neurofilament light chain, in a double-blinded randomized controlled trial (RCT) over 3 months in older adults. We will also examine the secondary effects of the supplement of quality of life and cognitive function.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo

Oslo, Norway

Location status: Recruiting

Location contact

Stine G Ulven, PhD

PRINCIPAL_INVESTIGATOR

Stine Ulven, PhD

CONTACT

[email protected]

+4722840208

Tahreem G Siddiqui, PhD

CONTACT

[email protected]

+4722840208

Tahreem G Siddiqui, PhD

SUB_INVESTIGATOR

About this study

We will assess the effects of combined supplementation of B-vitamins and omega-3 fatty acids on neurofilament light chain (NfL), a biomarker of brain atrophy, in a group of older adults. The primary outcome is the change in plasma NfL, which is a marker related to inflammation, brain atrophy, and worsening of cognitive performance. The secondary outcomes are related to change in plasma homocysteine, B-vitamins, EPA, DHA, omega-3 index (the percentage of EPA and DHA in red blood cells), and biological age using epigenetic markers. These are biomarkers that can tell us about the effect of the supplement in the body. We also want to study the effect of the intervention on gene expression profiles and metabolite profiles. In addition, we will include secondary outcome measures of quality of life (SF-36) that include affective symptoms, as these can be a forerunner to developing cognitive impairment. We are also collecting data on their cognitive performance, as this is related to brain atrophy and neurological conditions.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age > 65 years
  • A low baseline B-vitamin status as assessed by plasma tHcy > 11 μmol/L
  • Normal MMSE score (>25)

Exclusion criteria

  • Unable to give informed consent
  • Fatty fish intake > 2 times per week
  • daily omega-3 supplementation
  • daily B-vitamin supplementation
  • history of B12-injections
  • Serum creatinine > 90 μmol/L for women and > 105 μmol/L for men (above reference values)
  • aspirin use
  • renal disease
  • active cancer
  • Participants can be included if they accept to not take omega-3 supplementation or B-vitamin supplements during the study. They should stop using it and wait 12 weeks before they are invited to a screening visit.

Treatment and study plan

Intervention

Dietary Supplement

The intervention group will receive daily supplementation of one pill of B-vitamins (0.5 mg B12, 0.8 mg folate, 10 mg B6 and 10 mg riboflavin) + six pills of 500 mg Lysoveta, in total 3 g Lysoveta (480 mg EPA, 240 mg DHA). Lysoveta is an LPC-bound EPA/DHA supplement from krill which Aker BioMarine has recently developed.

Control

Other

The control group will receive daily supplementation of one placebo pill matching the B-vitamins and one placebo pill matching Lysoveta. the placebo capsules will contain 500 mg of mixed vegetable oil (comprising a blend of olive-, maize-, and palm kernel oil and medium-chain triglycerides, in a ratio of 4:4:3:2)

Primary outcomes

  1. Neurofilament light chain (NfL)

    Time frame: 3 months

    To assess the effects of combined supplementation of B-vitamins and omega-3 fatty acids on neurofilament light chain (NfL), a biomarker of brain atrophy in a group of elderly

Secondary outcomes

  1. Cognitive function

    Time frame: 3 months

    Neuropsychological tests of global and domain specific cognitive functions will be assessed using a test battery that includes the Mini-Mental state Examination, Cognistat, and Cerad test battery (working memory, verbal fluency, constructional praxis).

  2. Change in plasma homocysteine

    Time frame: 3 months

    Change in plasma homocysteine

  3. B-vitamins

    Time frame: 3 months

    B-vitamins (B12, folate, B6 and riboflavin)

  4. Omega-3

    Time frame: 3 months

    EPA, DHA, omega-3 index (the percentage of EPA and DHA in red blood cells)

Other outcomes

  1. Biological age

    Time frame: 3 months

    Biological age using epigenetic clocks

  2. Biomarkers of brain atrophy,

    Time frame: 3 months

    p-tau, inflammation,

  3. Quality of life in older adults

    Time frame: 3 months

    Quality of life RAND SF-36

  4. Transcriptome PBMC

    Time frame: 3 months

    Biomarker

  5. Metabolome in plasma

    Time frame: 3 months

    Biomarker

  6. Gut microbiome

    Time frame: 3 months

    Biomarker

Study contacts

Contact information is provided by the study sponsor or research team.

Stine M Ulven, PhD

CONTACT

[email protected]

+4722840208

Tahreem G Siddiqui, PhD

CONTACT

[email protected]

+4722840208 ext. +47

Sponsors and collaborators

Lead sponsor

University of Oslo

Other

Collaborators

  • Aker BioMarine
  • Heinrich-Heine University, Duesseldorf
  • Maastricht University
  • University of Dublin, Trinity College
  • University of Ulster

Registry information

Official study title

B-vitamins and ω-3 Fatty Acids to Modulate Brain Ageing in European Citizens Through Improved Nutrition: the BOOMERANG Project

Acronym: BOOMERANG

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Dec 31, 2025
Registry last updated
Dec 31, 2025

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.

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