- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07265648
Assessing Diet, Stress Scores, and Other Health Metrics in Healthy Northern California Adults
January 27, 2026 updated by: USDA, Western Human Nutrition Research Center
Characterization, Perceived Stress Scores, Nut Consumption and Bowel Patterns of a Healthy Adult Population in Northern California: A Pilot Study
The purpose of this study is to gather health and nutrition data from the population of Davis, CA and surrounding areas.
This data will be used to help us test and improve our study procedures for a larger planned study on peanut consumption and effects on cardiovascular disease (CVD) risk.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Participants will be recruited to complete an online survey asking questions about their stress levels, nut consumption, bowel patterns, body measurements, and county of residence.
This data will be used to gain insight into the characteristics of this population.
Study Type
Observational
Enrollment (Actual)
300
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
-
-
California
-
Davis, California, United States, 95616
- USDA Western Human Nutrition Research Center
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Adults 18-65 years old, currently living in Yolo, Sacramento, Solano, Sutter, or Placer counties
Description
Inclusion Criteria:
- Adults 18-65 years old
- Currently living in Yolo, Sacramento, Solano, Sutter, or Placer counties
- Able to complete an online survey written in English, on mobile phone, tablet, or computer
Exclusion Criteria:
- Previous participation in the study
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Adults living in and around Davis, CA
Adults 18-65 years old, currently living in Yolo, Sacramento, Solano, Sutter, or Placer counties
|
Online survey containing a Perceived Stress Score - 4 instrument, a modified food frequency questionnaire, and will measure reported age, sex, geographical location, usage of prescription medications, food allergies, and stool frequency and consistency.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Score
Time Frame: Baseline
|
Measured using a validated tool for assessing perceived psychosocial stress within the last month, the Perceived Stress Scale 4 (PSS-4).
Participants will report their answers to 4 questions in frequencies ranging from "Never" to "Very Often" on a 5 point scale
|
Baseline
|
|
Nut Consumption Frequency and Quantity
Time Frame: Baseline
|
Participants will input frequencies of nut and nut butter consumption and amounts of nuts and nut butter consumed in a typical month, using a modified food frequency questionnaire.
Frequency will be reported as values ranging from "Never" to "6 or more times a week".
Nut and nut butter consumption will be reported in cups and tablespoons
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Consumption Frequency of Nut-Containing Foods
Time Frame: Baseline
|
Reported as monthly consumption of nut containing foods (granola, cereal, pastries, breads, or other snacks or sweets) in frequencies ranging from "Never" to "6 or more times per week"
|
Baseline
|
|
Prevalence of Food Allergies
Time Frame: Baseline
|
Reported as allergies to any of 9 common food allergens: (Peanuts, Tree Nuts, Egg, Wheat, Soy, Shellfish, Fish, Sesame, and Milk)
|
Baseline
|
|
Stool Frequency
Time Frame: Baseline
|
Reported as usual number of bowel movements per week
|
Baseline
|
|
Stool Consistency
Time Frame: Baseline
|
Reported using images of Bristol Scale stool types
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Baseline
|
|
Body Mass Index (BMI)
Time Frame: Baseline
|
Calculated using participant-reported height and weight
|
Baseline
|
|
Prescription Drug Use
Time Frame: Baseline
|
Participants will confirm or deny intake of medications from 6 categories: (Asthma medications, Antibiotics or antivirals, weight loss medications, cholesterol or lipid lowering medications, blood pressure medications, or psychiatric medications)
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Baseline
|
|
Age
Time Frame: Baseline
|
Reported as age in years
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Baseline
|
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Biological Sex
Time Frame: Baseline
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Reported as sex assigned at birth
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Baseline
|
|
Geographic Data
Time Frame: Baseline
|
Reported as current county of residence
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ryan Snodgrass, PhD, United States Department of Agriculture - Western Human Nutrition Research Center
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)
December 8, 2025
Primary Completion (Actual)
January 20, 2026
Study Completion (Actual)
January 20, 2026
Study Registration Dates
First Submitted
November 20, 2025
First Submitted That Met QC Criteria
December 1, 2025
First Posted (Actual)
December 5, 2025
Study Record Updates
Last Update Posted (Actual)
January 29, 2026
Last Update Submitted That Met QC Criteria
January 27, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2337131
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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