- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04484974
Effects of Pecan Nut Snacks v Equicaloric Snacks on Appetite, Food Intake, Metabolism, Hormones and Biomarkers
July 2, 2024 updated by: University of Colorado, Denver
A Randomized, Two Condition, Crossover Trial Assessing Appetite, Energy Metabolism, Blood Biomarker and ad Libitum Food Intake Responses to a Mid-morning Pecan Snack vs. an Equicaloric High Carbohydrate Savory Snack in Healthy Volunteers With Overweight/Obesity
This is a within-subjects crossover study that examines subjective appetite, food intake, hormone and metabolic responses to consumption of mid morning snacks of pecan nuts as compared to an iso-caloric amount of tortilla chips.
Pecans are high in fat and calories and low in carbohydrate by weight, while tortilla chips are mostly carbohydrate and essentially devoid of fat.
These two very different nutrient profiles should elicit different metabolic and biomarker responses.
The study aims to determine whether these treatments also elicit different subjective appetite and food intake responses.
Participants will be healthy volunteers with overweight and obesity, a population that may be seeking healthy snacking options that are satisfying and satiating.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a randomized, two condition, crossover study in healthy individuals with overweight and obesity examining the effect of a mid-morning snack of pecans vs. a low fat savory snack on appetite, energy expenditure, blood biomarkers of appetite and metabolism and ad libitum food intake at lunch.
Twenty-four participants will be enrolled and studied on two test days with at least one week washout in between.
On test days, participants will have baseline measures of appetite (by Visual Analogue Scale (VAS)), blood hormones and substrates, and energy expenditure and fuel oxidation (Resting Metabolic Rate (RMR), by indirect calorimetry) taken just prior to consuming a standardized 300 kcal breakfast.
VAS measures will be taken at 20, 30, 60, 90 and 120 min following the meal and RMR will be measured for 20 min after eating.
A mid-morning snack of either 250 kcal of pecans or lightly salted tortilla chips will be consumed and VAS and blood measures will be taken at 20, 30, 60, 90 and 120 min following the snack and RMR will be measured for 20 min after eating.
Participants will be given an ad libitum lunch meal and VAS and blood measures will be taken at 20, 30, 60, 90 and 120 min following the lunch and RMR will be measured for 20 min after eating.
Blood will be analyzed for glucose, insulin, free fatty acids, triglycerides, ghrelin, leptin, PYY, and GLP-1.
Two hypotheses will be examined: 1. pecans will provoke greater feelings of fullness and reduced hunger after the snack and lunch meal consumption (on either a calorie per calorie or volume basis) as compared to the tortilla chip snack, and 2. the pecan snack will provoke greater responses of satiety hormones compared to tortilla chips.
Post-snack and lunch energy expenditure and fat oxidation will also be compared between treatments as an exploratory aim.
Study Type
Interventional
Enrollment (Actual)
21
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Colorado
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Aurora, Colorado, United States, 80045
- University of Colorado Anschutz Health and Wellness Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 35 adult men and women
- all ethnic groups
- ages 20-50,
- BMI 27-35,
- habitually eat breakfast,
- willing to eat the test snacks and other foods offered,
- weight stable for the last 6 months
- willing to consent and adhere to the test procedures and schedule
Exclusion Criteria:
- nut allergies,
- uncontrolled thyroid disorders,
- diabetes mellitus,
- eating disorders,
- pregnant, or planning to become pregnant during the study,
- lactating,
- uncontrolled hypertension,
- active dieting
- intensive physical activity training regimen (>300 min/wk exercise),
- medical history or current medication that may affect study outcomes per study PI discretion
- consuming pecans on a regular basis
- unable to lie still with a clear hood over their head for the measurement of energy expenditure
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Pecan snack condition
In this crossover condition, a mid morning snack consisting of 250 kcal of lightly salted roasted pecan nuts will be administered.
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Under this condition, each participant will consume a mid morning snack of pecans followed by an ad libitum lunch.
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Active Comparator: Tortilla chip snack condition
In this crossover condition, a mid morning snack consisting of 250 kcal of lightly salted pretzels will be administered.
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Under this condition, each participant will consume a mid morning snack consisting of an iso-caloric (equal to the pecan snack) snack of tortilla chips followed by an ad libitum lunch.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline (before snack consumption) to 120 minutes in subjective appetite response to pecan or pretzel snack using visual analog assessment
Time Frame: Baseline (prior to mid-morning snack consumption) to 120 minutes after snack consumption at 20, 30, 60, 90 and 120 minutes following consumption.
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Subjective appetite will be assessed using a visual analog scale.
Subjective feelings will be rated on a 100 mm horizontal line preceded by the questions: "How hungry are you right now?" and anchored on the left by "not at all hungry" and by "extremely hungry" on the right; Fullness will be queried by "How full do you feel right now?" anchored by "not at all..." and "extremely..."; Desire to eat will be queried by, "How strong is your desire to eat right now?" anchored by anchored by "not at all..." and "extreme...; and prospective consumption will be queried by, "how much food do you think you can you eat right now" with anchors of "not (much) at all" to "extremely/an extreme amount".
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Baseline (prior to mid-morning snack consumption) to 120 minutes after snack consumption at 20, 30, 60, 90 and 120 minutes following consumption.
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Change from baseline (prior to lunch) to 120 minutes in subjective appetite response to lunch meal using visual analog assessment
Time Frame: Prior to lunch consumption and at 20, 30, 60, 90 and 120 minutes following consumption.
|
Subjective appetite will be assessed using a visual analog scale.
Subjective feelings will be rated on a 100 mm horizontal line preceded by the questions: "How hungry are you right now?" and anchored on the left by "not at all hungry" and by "extremely hungry" on the right; Fullness will be queried by "How full do you feel right now?" anchored by "not at all..." and "extremely..."; Desire to eat will be queried by, "How strong is your desire to eat right now?" anchored by anchored by "not at all..." and "extreme...; and prospective consumption will be queried by, "how much food do you think you can you eat right now" with anchors of "not (much) at all" to "extremely/an extreme amount".
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Prior to lunch consumption and at 20, 30, 60, 90 and 120 minutes following consumption.
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Energy intake response to pecan or pretzel snack using weighed food intake measures
Time Frame: 30 minutes allowed for completion of the lunch meal
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Energy intake at ad libitum lunch meal consisting of a variety of different foods offering approximately 1400 of kilocalories of energy having an overall composition of approximately 15% protein, 55% carbohydrate and 30% fat.
Twelve ounces of water will be provided as the beverage.
Energy intake will be calculated from the weight of each food consumed and the published nutrient composition of the foods.
Linear mixed effects model will be used to test the difference in energy intake between two experimental conditions.
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30 minutes allowed for completion of the lunch meal
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Change from baseline (prior to snack consumption) to 120 minutes in serum glucose following pecan or pretzel snack consumption.
Time Frame: Baseline (prior to snack) to 120 minutes at intervals of 20, 30, 60, 90 and 120 minutes.
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Serum glucose by enzymatic method.
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Baseline (prior to snack) to 120 minutes at intervals of 20, 30, 60, 90 and 120 minutes.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum glucose following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum glucose by enzymatic method.
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum insulin following pecan or pretzel snack consumption.
Time Frame: Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum insulin by radio-immunoassay.
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Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum insulin following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum insulin by radio-immunoassay.
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum triglycerides following pecan or pretzel snack consumption.
Time Frame: Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum triglycerides by enzymatic assay.
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Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum triglycerides following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum triglycerides by enzymatic assay.
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum free fatty acids following snack consumption.
Time Frame: Prior to mid-morning snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum free fatty acids by enzymatic assay.
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Prior to mid-morning snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum free fatty acids following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum free fatty acids by enzymatic assay.
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum ghrelin following snack consumption.
Time Frame: Prior to mid-morning snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum ghrelin by radio-immunoassay
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Prior to mid-morning snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum ghrelin following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum ghrelin by radio-immunoassay
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum peptide YY following snack consumption.
Time Frame: Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum peptide YY (PYY) by radio-immunoassay
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Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum peptide YY following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum peptide YY (PYY) by radio-immunoassay
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change from baseline (prior to snack consumption) to 120 minutes in serum glucagon like peptide-1 following snack consumption.
Time Frame: Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Serum glucagon like peptide-1 (GLP-1) by enzyme immunoassay
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Prior to snack and at intervals of 20, 30, 60, 90 and 120 minutes after snack consumption.
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Change from baseline (prior to lunch consumption) to 120 minutes in serum glucagon like peptide-1 following lunch consumption.
Time Frame: Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Serum glucagon like peptide-1 (GLP-1) by enzyme immunoassay
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Prior to lunch and at intervals of 20, 30, 60, 90 and 120 minutes after lunch consumption.
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Change in serum leptin from baseline to 120 minutes following snack consumption
Time Frame: Baseline (prior to breakfast) and at 120 minutes following mid-morning snack consumption.
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Serum leptin by immunoassay.
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Baseline (prior to breakfast) and at 120 minutes following mid-morning snack consumption.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change from baseline in energy expenditure post snack
Time Frame: Resting energy expenditure will be measured for 20 minutes after snack consumption.
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Post snack resting energy expenditure will be measured using hood indirect calorimetry.
Energy expenditure will be measured using standard indirect calorimetry with the ventilated hood technique (Parvo Medics Truemax 2400, Salt Lake City, UT).
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Resting energy expenditure will be measured for 20 minutes after snack consumption.
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Change from baseline in energy expenditure post lunch
Time Frame: Resting energy expenditure will be measured for 20 minutes after lunch consumption.
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Post lunch resting energy expenditure will be measured using hood indirect calorimetry.
Energy expenditure will be measured using standard indirect calorimetry with the ventilated hood technique (Parvo Medics Truemax 2400, Salt Lake City, UT).
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Resting energy expenditure will be measured for 20 minutes after lunch consumption.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: John C Peters, PhD, University of Colorado, Denver
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 23, 2020
Primary Completion (Actual)
September 19, 2023
Study Completion (Actual)
September 19, 2023
Study Registration Dates
First Submitted
June 26, 2020
First Submitted That Met QC Criteria
July 21, 2020
First Posted (Actual)
July 24, 2020
Study Record Updates
Last Update Posted (Actual)
July 5, 2024
Last Update Submitted That Met QC Criteria
July 2, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20-0048
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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