Cognitive Change Clinical Trial
Official title:
WHNRC (Western Human Nutrition Research Center) Honey Study
The purpose of this research is to compare two snacks, one with honey and nuts and the other with sugar and nuts, on glucose levels before and after eating these snacks. The investigators hypothesize that honey and nuts will have an additive effect on the reduction of postprandial glucose response. The investigators further hypothesize that consumption of honey paired with nuts will retain the benefit of sugar consumption in satiety and reduction of metabolic stress.
Status | Recruiting |
Enrollment | 80 |
Est. completion date | September 30, 2026 |
Est. primary completion date | January 2, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - Women must be pre-menopausal - Willing to consume snacks that contain honey, table sugar, and tree nuts Exclusion Criteria: - Body Mass Index (BMI) <18.5 or >40 - Allergies to tree nuts - Current medical diagnoses of chronic diseases including cardiovascular or pulmonary diseases, renal diseases, cancer, type 1 or type 2 diabetes, thyroid disease requiring medication, inflammatory or irritable bowel diseases, or those with recent major surgeries - No individuals who fall in to the vulnerable categories of adults including those unable to consent, pregnant women, children, or prisoners will be eligible for this study - Routinely taking medications known to affect glucose response. - Caffeine and alcohol use will not be excluded, but should be carefully reported by each subject. Regarding female candidates: - Post-menopausal - Women who have been pregnant or nursing within the last 6 months or plan to become pregnant during the trial will be ineligible |
Country | Name | City | State |
---|---|---|---|
United States | USDA, ARS, Western Human Nutrition Research Center | Davis | California |
Lead Sponsor | Collaborator |
---|---|
USDA, Western Human Nutrition Research Center | National Honey Board |
United States,
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Bach-Faig A, Berry EM, Lairon D, Reguant J, Trichopoulou A, Dernini S, Medina FX, Battino M, Belahsen R, Miranda G, Serra-Majem L; Mediterranean Diet Foundation Expert Group. Mediterranean diet pyramid today. Science and cultural updates. Public Health Nutr. 2011 Dec;14(12A):2274-84. doi: 10.1017/S1368980011002515. — View Citation
Carroll JF, Kaiser KA, Franks SF, Deere C, Caffrey JL. Influence of BMI and gender on postprandial hormone responses. Obesity (Silver Spring). 2007 Dec;15(12):2974-83. doi: 10.1038/oby.2007.355. — View Citation
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Gonzalez-Rodriguez M, Pazos-Couselo M, Garcia-Lopez JM, Rodriguez-Segade S, Rodriguez-Garcia J, Tunez-Bastida C, Gude F. Postprandial glycemic response in a non-diabetic adult population: the effect of nutrients is different between men and women. Nutr Metab (Lond). 2019 Jul 17;16:46. doi: 10.1186/s12986-019-0368-1. eCollection 2019. — View Citation
Gourdomichali T, Papakonstantinou E. Short-term effects of six Greek honey varieties on glycemic response: a randomized clinical trial in healthy subjects. Eur J Clin Nutr. 2018 Dec;72(12):1709-1716. doi: 10.1038/s41430-018-0160-8. Epub 2018 Apr 24. — View Citation
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in postprandial glucose response | Interstitial glucose response measured by a continuous glucose monitor | Measured continuously over days 0-8 and 23-31 | |
Secondary | Change in Self-reported hunger | Responses regarding hunger will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Self-reported fullness | Responses regarding fullness will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Self-reported desire to eat | Responses regarding desire to eat will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Self-reported satisfaction with snack | Responses regarding satisfaction with snack will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Self-reported prospective consumption | Responses regarding prospective consumption will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Self-reported nausea | Responses regarding nausea will be collected using a visual analog scale on a tablet with a 0-100 scale depicting the extremes (0= not at all to 100= extremely) | Fasting and 30, 60, and 90 min after consumption of standard breakfast on days 4, 8, 27, and 31 | |
Secondary | Change in Cognitive testing for Spatial Working Memory | Cambridge Neuropsychological Test Automated battery (CANTAB) software will be used to assess Spatial Working Memory (SWM) | Days 4, 8, 27, and 31 | |
Secondary | Change in Cognitive testing for Paired Associates Learning | CANTAB software will be used to assess Paired Associates Learning (PAL) | Days 4, 8, 27, and 31 | |
Secondary | Change in Cognitive testing for Rapid Visual Processing | CANTAB software will be used to assess Rapid Visual Processing (RVP) | Days 4, 8, 27, and 31 | |
Secondary | Change in Salivary cortisol | Metabolic stress will be analyzed by measuring cortisol in saliva samples | Day 0 and 23 fasting only. Days 4, 8, 27, and 31 at fasting, 30, 60 and 90 min after consumption of snack provided in standard breakfast | |
Secondary | Assessment of Fasted Salivary Estradiol | Passive drool will be assayed for estradiol as they impact metabolic stress throughout study days | Days 0, 4, 8, 23, 27,and 31 at fasting only | |
Secondary | Assessment of Fasted Salivary Progesterone | Passive drool will be assayed for progesterone as they impact metabolic stress throughout study days | Days 0, 4, 8, 23, 27,and 31 at fasting only | |
Secondary | Change in Stool marker of inflammation | Fecal calprotectin measured in stool samples | Stool collected on study days 0, 4, 8, 23, 27, and 31 | |
Secondary | Change in Stool bacterial metagenomics | Honey responsive genes identified by metagenomics | Stool collected on study days 0, 4, 8, 23, 27, and 31 | |
Secondary | Change in Dietary Intake | Food records collected using Automated Multi-pass Method (AMPM) on the platform ASA24 | Days 1-3, 5-7, 24-26, and 28-30 |
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