Aging Clinical Trial
Official title:
Role of Hazelnut Consumption in Improving Micronutrient Status in Older Adults
NCT number | NCT03485989 |
Other study ID # | 6988 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 22, 2016 |
Est. completion date | December 29, 2017 |
Verified date | August 2019 |
Source | Oregon State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
With advancing age, older adults are susceptible to vitamin and mineral deficiencies for a
variety of reasons. Nutrient-dense food sources of vitamin E and other key vitamins and
minerals, like hazelnuts, may offer a simple means of improving nutritional status of healthy
older adults.
This hypothesis is that individuals eating hazelnuts everyday will result in measurable
increases in magnesium and vitamin E levels, two under-consumed micronutrients among older
adults. Thus, subjects will consume two ounces (56 g) of hazelnuts each day for sixteen
weeks. Investigators will measure vitamin E and magnesium levels along with a general
assessment of micronutrient status as primary outcomes. Since nuts are nutrient-rich sources
of unsaturated fatty acids but low in carbohydrates, changes in fasting glucose, lipid and
lipoprotein profiles, and BMI will also be determined (secondary outcomes).
Status | Completed |
Enrollment | 41 |
Est. completion date | December 29, 2017 |
Est. primary completion date | September 18, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 55 Years and older |
Eligibility |
Inclusion Criteria: - Must be generally healthy - Women must be post-menopausal (12 months period-free) or surgically sterile. - Must be willing to eat two ounces (56 g) of dry roasted hazelnuts each day during the study - Must refrain from taking nutritional supplements during the study - Must follow a diet that excludes all nuts (other than those supplied), seeds, and other vitamin E-rich foods (see Restricted Foods and Supplements document) - Must be willing to complete food frequency questionnaires - Must be willing to give blood samples on 3 separate occasions and urine on 2 separate occasions Exclusion Criteria: - Current or past (two years) use of any tobacco (including e-cigarettes) and marijuana products - Allergy to any nut including tree nuts and peanuts, or hazelnut pollen - History of asthma - Vitamin E supplement use during the last three months or regular use of vitamin E-enriched nutritional drinks (e.g. Ensure) - Regular nut eaters: individuals that regularly consume > 3.5 ounces (112 g) of almonds, hazelnuts and/or sunflower seeds per week in any form (e.g. nuts, nut butters, nut oil, etc.), and no more than 10 mg alpha-tocopherol (vitamin E) per day from their diet. - Bariatric surgery (e.g. gastric bypass, gastric banding, sleeve gastrectomy, etc.), or serious chronic illness including Crohn's disease, celiac disease, diverticulitis, chronic diarrhea, ulcerative colitis, gastritis - History of cardiovascular disease including stroke, heart attack, or congestive heart failure - Any history of arterial bypass or stent placement. - History of emphysema or chronic obstructive pulmonary disease (COPD) - Stage II hypertension (either systolic pressure > 159 mm Hg or diastolic pressure 99 mm Hg) - History of cancer during the previous 5 years - Diabetes (type 1 or type 2) or use of drugs to lower blood sugar or increase insulin production or sensitivity - Use of medications to lower cholesterol other than statins - Use of medications to decrease fat or cholesterol absorption - Unwillingness to refrain from taking dietary supplements (except calcium and vitamin D and vitamin B12), magnesium-containing drugs such as certain antacids, stool softeners and laxatives - BMI < 18.5 or > 35 - Blood chemistry limits; any of the following at screening excludes participation: - Fasting blood glucose = 126 mg/dL - LDL cholesterol =160 mg/dL - Triglyceride =200 mg/dL - High-sensitivity C-reactive protein (hsCRP) > 10 mg/L |
Country | Name | City | State |
---|---|---|---|
United States | Linus Pauling Science Center | Corvallis | Oregon |
Lead Sponsor | Collaborator |
---|---|
Oregon State University | Hazelnut Marketing Board |
United States,
Michels AJ, Leonard SW, Uesugi SL, Bobe G, Frei B, Traber MG. Daily Consumption of Oregon Hazelnuts Affects a-Tocopherol Status in Healthy Older Adults: A Pre-Post Intervention Study. J Nutr. 2018 Dec 1;148(12):1924-1930. doi: 10.1093/jn/nxy210. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in Plasma Micronutrient Levels | Plasma levels of magnesium and vitamin E (alpha and gamma tocopherol) at baseline and 16 weeks after hazelnut intervention will be determined. Vitamin E analyses will be performed as absolute concentrations and concentrations corrected for total plasma lipids. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Primary | Changes in Plasma Urine Vitamin E Metabolites | Urine concentrations of alpha and gamma carboxyethyl hydroxychroman (metabolites of alpha and gamma tocopherol, respectively) will be determined at baseline and 16 weeks after hazelnut intervention. Urine values will be corrected for creatinine levels. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Primary | Changes in Lymphocyte Proliferation Assay | Blood samples will be collected and sent to Spectracell Labs, Inc. for a functional micronutrient analysis utilizing their proprietary lymphocyte proliferation assay. Micronutrient levels in these white blood cell samples will be assessed by changes in lymphocyte proliferation in the absence of a given vitamin or mineral, suggesting functional inadequacies that may not correspond to plasma values. Data will be represented as percent difference in cell proliferative capacity in cells growing in a complete media vs. a single-nutrient deprived media. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Secondary | Lipid Status | Lipid profile will be determined from samples blood sent to a CLIA(Clinical Laboratory Improvement Amendments)-certified laboratory. Changes to fasting lipoprotein and triglyceride status determined before and after hazelnut intervention. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Secondary | Glucose Homeostasis | Glucose and insulin levels will be determined from blood samples to a CLIA-certified laboratory. Changes to fasting glucose levels and insulin levels determined before and after hazelnut intervention. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Secondary | BMI | Height and weight will be measured by stadiometer and scale. Changes to height and weight will be expressed as BMI calculated before and after hazelnut intervention. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Secondary | Blood Pressure | Changes to resting systolic and diastolic blood pressure (mmHg) will be measured by sphygmomanometer before and after hazelnut intervention. | Between baseline (Visit 2) and 16 weeks (last visit) | |
Secondary | Heart Rate | Resting heart rate will be measured manually using the ventral aspect of radial artery. | Between baseline (Visit 2) and 16 weeks (last visit) |
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