Skip to content
Bored Studies
RecruitingAccepts healthy volunteersPhase 2

ALA-enriched Nutrition for Prevention of Cognitive Decline in APOE4 Older Adults

Michal Schnaider Beeri, Ph.D. · NCT07392723

View Study & Apply (opens in a new tab)

Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 60+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 2
Target enrollment
20
US sites recruiting
1
Study start
January 12, 2025
Record last updated
February 6, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This randomized, double-blind, placebo-controlled pilot trial will evaluate the effects of alpha-linolenic acid (ALA) supplementation on cognitive function, blood-brain barrier integrity, and brain vascular health in older adults with mild cognitive impairment and APOE4 genotype. By targeting the endogenous synthesis of docosahexaenoic acid (DHA) through ALA supplementation, the investigators aim to overcome the limitations of direct DHA supplementation, particularly in APOE4 carriers who exhibit low brain DHA levels and impaired blood-brain barrier function. This innovative approach offers a safe, cost-effective, and easily implementable therapeutic strategy for older adults at high risk for Alzheimer's dementia, especially APOE4 carriers, addressing a critical need given the limited cognitive benefits and significant adverse events of current amyloid-clearing drugs in this population.

Being studied: Alpha-Linolenic Acid (2.6 g/day); Placebo Control Group

Conditions: Cognitive Dysfunction; Alzheimer Disease; Blood-Brain Barrier; Apolipoprotein E, Deficiency or Defect of; Brain Aging; Fatty Acids, Omega-3

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Age 60 years or older
  • Have amnestic Mild Cognitive Impairment (MCI) - memory problems that do not interfere with daily life.
  • Carry at least one APOE4 gene allele (determined by a blood test).
  • Be fluent in English or Spanish.
  • Have a study partner (family member or friend) who can provide information about daily function.
  • Have the ability to give informed consent and comply with study visits and procedures.

Exclusion Criteria

  • A diagnosis of dementia or any other brain disease that significantly affects thinking or memory (e.g., Alzheimer's disease, Parkinson's disease, schizophrenia, epilepsy, traumatic brain injury).
  • History of stroke or other major neurological condition.
  • Short life expectancy due to end-stage disease or other serious medical condition.
  • Active cancer treatment that could interfere with study participation.
  • Allergy or sensitivity to flaxseed oil or corn oil.
  • Current use of flaxseed, flax oil, or fish oil supplements more than once per week.
  • MRI contraindications, such as pacemakers, metallic implants, or severe claustrophobia.
  • Current or past history of prostate cancer, regardless of remission status, OR a prostate-specific antigen (PSA) level > 20 ng/mL at screening.
  • Use of experimental Alzheimer's treatments (e.g., amyloid monoclonal antibodies) unless on a stable regimen as confirmed by the treating physician.

Recruiting US locations

  • Rutgers - Institute for Health

    New Brunswick, NJ 08901

    Site contact: Claudio Mendes · claudio.mendes@rutgers.edu

Study contacts (from the official record)

  • Claudio Mendes, MS · 8489328412 · alastudy@njms.rutgers.edu
  • Rebecca West-Mortimer, PHD · 8489328415 · alastudy@njms.rutgers.edu
All heart & blood pressure studies in New Jersey →
ALA-enriched Nutrition for Prevention of Cognitive Decline in… (NCT07392723) | Bored Studies