Impact of walnuts on brain health and gut bacteria in older adults
Effect of Walnuts on Cognitive Function and Gut Microbiome in Older Adults
This study tests if eating walnuts every day for 12 weeks can help improve brain health and gut bacteria in healthy adults aged 55 and older.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 55 Years and up |
| Sex | All |
| Sponsor | Oregon State University Academic / other |
| Locations | 1 site (Corvallis, Oregon) |
| Trial ID | NCT06942351 on ClinicalTrials.gov |
What this trial studies
This study investigates how daily walnut consumption for 12 weeks affects cognitive function, inflammation markers, and the gut microbiome in healthy adults aged 55 and older. Participants will consume walnuts and undergo cognitive tests to assess any improvements in brain health. The study aims to explore the relationship between walnut intake, gut microbiota changes, and cognitive decline associated with aging.
Who should consider this trial
Good fit: Ideal candidates are healthy adults aged 55 years and older who can comply with the study's dietary restrictions and cognitive assessments.
Not a fit: Patients with severe cognitive impairment or those unable to adhere to dietary restrictions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into dietary interventions that enhance cognitive function and gut health in older adults.
How similar studies have performed: While studies on dietary impacts on cognitive function exist, this specific approach focusing on walnuts and gut microbiome interactions is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Corvallis, Oregon
- Oregon State University — Corvallis, Oregon, United States (Recruiting)
Study contacts
- Principal investigator: Emily Ho, PhD — Oregon State University
- Study coordinator: Emily Ho, PhD
- Email: emily.ho@oregonstate.edu
- Phone: 541-737-9559
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.