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NCT Number: NCT06942351

Effect of Walnuts on Cognitive Function and Gut Microbiome in Older Adults

The purpose of this study is to examine the impact of daily consumption of walnuts for 12 weeks on cognitive function, markers of inflammation and oxidative stress, and the gut microbiome in healthy adults age 55 years and older.

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Key information

Age range

55 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oregon State University

Corvallis, Oregon, 97331, United States

Location status: Recruiting

Location contact

Emily Ho, PhD

PRINCIPAL_INVESTIGATOR

Sandra Uesugi, RN, BSN, MS

CONTACT

[email protected]

541-737-3594

About this study

The investigators will determine the extent to which daily consumption of walnuts by older adults for 12 weeks influences cognitive function and whether improvements are associated with changes in the resident gut microbiota. The investigators propose that age-related cognitive decline can be mitigated by consuming walnuts, by modulating the microbiota and microbial metabolites and decreasing oxidative stress and inflammation.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 55 years or older
  • Able to hear well enough to understand spoken instructions and questions
  • Able to see well enough to read and respond to printed instructions and fill out questionnaires (corrective lenses are allowed)
  • Able to write legibly and move a computer joystick with at least one hand (i.e., no injury or connective tissue or joint disorder that would impair ability to write or make hand movements)
  • Able to speak, read, and understand English
  • Score of greater than 79 on water maze learning task
  • Willing to maintain current eating patterns
  • Willing and able to complete the cognitive tests
  • Willing to stop consuming almonds, Brazil nuts, cashews, chestnuts, hazelnuts, macadamia nuts, peanuts, pecans, pistachios, walnuts, persimmons and pomegranates for 14 weeks. - are nuts or contain ellagitannins or ellagic acid - compounds/foods of interest for this study
  • Willing to limit oak aged wines and spirits to 1 serving/day and limit blackberries (including similar berries like boysenberries, marionberries, and olallieberries), cloudberries, cranberries, currants, elderberries, lingonberries, raspberries, strawberries, wolfberries, other native berries; guava, mango, muscadine grapes, nectarines, peaches, plums, pluots to 1 cup/day for 14 weeks; REMAIN CONSISTENT (consistent intake levels of): Coffee, tea, apple, apricots, blueberries, cherries, grapes (table/common)
  • Willing to stop probiotic supplements 2 weeks prior to and during the study (14 weeks)

Exclusion criteria

  • Consumption of walnuts, pecans, and chestnuts combined greater than 2 oz / week in the past 3 months.
  • Use of oral antibiotics in the past month
  • Regular use of oral anti-inflammatory medications in the past month
  • Nut, wheat, or gluten allergy/intolerance
  • Pregnant or planning to become pregnant during the study period
  • Weighs less than 110 pounds
  • Diagnosis of sickle cell disease
  • Susceptibility to motion sickness
  • Consumes 3 or more alcoholic drinks daily
  • History of smoking tobacco products, including e-cigarettes and vaporizers in the past 2 years (smokeless tobacco use not exclusionary)
  • Use of psilocybin or cannabis products (including CBD-only products) in the past 2 years
  • Current treatment for alcohol or other substance use disorder
  • History of heart attack, heart failure, or stroke, including transient ischemic attack
  • History of liver disease or kidney disease requiring dialysis
  • History of cancer in the past 5 years (Skin cancer that was only surgically treated is not exclusionary)
  • History of bariatric surgery (e.g., gastric bypass, gastric banding, sleeve gastrectomy, etc.) or disorders (e.g., Crohn's disease, unmanaged celiac disease, ulcerative colitis)
  • History of thyroid disorder that requires medication, but subject is not taking medication
  • History of chronic bronchitis or emphysema
  • Diagnosis of dementia or Alzheimer's disease
  • History of head injury requiring hospitalization or loss of consciousness > 5 minutes
  • History of chronic migraines (for at least 3 months, headache occurring on 15 or more days per month, where at least 8 of those headache days have migraine symptoms)
  • Blood pressure above 159 (systolic) or 99 (diastolic) mm Hg
  • Corrected vision worse than 20/50
  • Score of less than 10/15 on Ishihara color vision test or diagnosis of color blindness
  • Score of less than 26/30 on Mini-Mental State Exam
  • Score of greater than 15 on Center for Epidemiologic Depression survey
  • History of disease or disorder which causes cognitive impairment, including but limited to: attention-deficit/hyperactivity disorder (ADHD), amyotrophic lateral sclerosis, autism, bipolar disorder, Down's syndrome, encephalitis, epilepsy/seizures, human immunodeficiency virus (HIV), Huntington's disease, Korsakoff's psychosis, multiple sclerosis, Parkinson's disease, or psychotic disorders (e.g., schizophrenia, schizoaffective disorder, schizophreniform disorder)
  • Current and regular use of any of the following medications: insulin, opioids, anti-seizure medications, psychotropic medications: stimulants, anti-psychotics, or medications that cause daytime drowsiness or difficulty concentrating

Treatment and study plan

Walnuts

Other

Daily consumption of 1.5 ounces of plain walnuts for 12 weeks

Crackers

Other

Daily consumption of non-whole grain crackers for 12 weeks (caloric equivalent to 1.5 ounces of plain walnuts)

Primary outcomes

  1. Cognitive function - memory

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: age adjusted standard scores (higher score reflects positive outcome)

  2. Cognitive function - memory

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: proximity (lower score reflects positive outcome)

  3. Cognitive function - cognitive flexibility

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: age adjusted standard scores (higher score reflects positive outcome)

  4. Cognitive function - cognitive flexibility

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: proximity (lower score reflects positive outcome)

  5. Cognitive function - speed of processing

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: age adjusted standard scores (higher score reflects positive outcome)

  6. Gut microbiome composition

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: microbiome composition

  7. Lipid oxidation levels

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: plasma malondialdehyde (MDA)

  8. Gut permeability and health: Inflammatory biomarkers

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: Gut inflammatory biomarkers fecal calprotectin and myeloperoxidase

  9. Biomarkers of inflammation

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: Plasma inflammatory markers (ex. CRP and IL-6)

Secondary outcomes

  1. Urolithin concentrations

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: urolithin A and urolithin B concentrations in urine

  2. Blood pressure

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: systolic and diastolic blood pressure

  3. Weight

    Time frame: 0 and 12 weeks

    Change from baseline at week 12: weight

Study contacts

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

Emily Ho, PhD

CONTACT

[email protected]

541-737-9559

Sandra Uesugi, RN, BSN, MS

CONTACT

[email protected]

541-737-3594

Sponsors and collaborators

Lead sponsor

Oregon State University

Other

Collaborators

  • California Walnut Commission

Registry information

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Apr 24, 2025
Registry last updated
Jun 19, 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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