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Dietary QualityHerbSpicesDietNCT07082348

Feasibility and Potential Efficacy of Herbs and Spices for Improving Dietary Quality in College Students: A Pilot Study

A study testing Herbs and Spices Nutrition Education Program in people with Dietary Quality and Feasibility Studies, run by University of Nevada, Las Vegas at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this single-arm feasibility, pilot study is to assess the feasibility, acceptability, and potential effectiveness of the Herbs and Spices Nutrition Education Program (HSNP-focusing on incorporating herbs and spices into the diet for adherence to the DGA's) for determining the scalability of implementing… Read more about this study

Who is it for?
Ages 18 to 39 years
What is being tested?
Herbs and Spices Nutrition Education Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
3 Jul 2025to 6 Apr 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 39 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • College students (undergraduate and graduate)
  • Ages 18-39 years
  • BMI 18.5-40 kg/m
  • Having poor dietary quality (a Rapid Prime Diet Quality Score of 12 or below),
  • Maintain current lifestyle habits (e.g., medications/ supplement use, exercise, and sleep), and avoid taking new supplements or medications throughout the study.

Who cannot join

  • Individuals diagnosed with myocardial infarction within the past 6 months
  • Uncontrolled hypertension
  • BMIs <18.5 or >40 kg/m2
  • Autoimmune disease or immune compromised
  • A recent diagnosis of cancer or under current treatment for cancer
  • A history of kidney stones
Show all 17Show fewer
  • Having pacemaker
  • Participating in a weight loss program
  • Having a history of any significant GI disease
  • Insulin use
  • Currently on dialysis
  • Currently consuming pro-/pre-biotics or antiobiotics
  • Diagnosed with unstable chronic metabolic disease
  • Have allergies to any herbs and spices
  • Are pregnant/nursing
  • Participating in another investigational study
  • Unable or unwilling to give consent

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Department of Kinesiology and Nutrition Sciences, Las Vegas, Nevada

    Las Vegas, Nevada, 89154

Other trials in United States

About this study

Official title: Assessing the Feasibility and Potential Efficacy of Herbs and Spices for Improving Dietary Quality and Adherence to the Dietary Guidelines for Americans in College Students With Poor Dietary Quality: A Pilot Study

The goal of this single-arm feasibility, pilot study is to assess the feasibility, acceptability, and potential effectiveness of the Herbs and Spices Nutrition Education Program (HSNP-focusing on incorporating herbs and spices into the diet for adherence to the DGA's) for determining the scalability of implementing this intervention for a larger scale, more comprehensive study The main questions it aims to answer are:

  • What is the feasibility and acceptability of incorporating herbs and spices into the diet along with DGA-focused nutrition education through the HSNP in college students with poor dietary quality?
  • What are the preliminary effects of the HSNP on dietary intake/quality, cardiometabolic, and gut health in college students with poor dietary quality?
  • What are the barriers associated with HSNP implementation in college students with poor dietary quality?
Read more

Participants will:

  • Be asked to come to the study site initially for a Screening Study Visit to confirm eligibility.
  • Be asked to come the clinical study site for a Pre-HSNP and Post-HSNP Study Visit (within two weeks prior to starting the HSNP and after week 6 of completing the HSNP) for assessments of cardiometabolic and gut health.
  • Be asked to come to the Nutrition Center for weeks 1 and 3 of the HSNP, where they will receive education on the Dietary Guidelines for Americans and the health benefits of herbs and spices, have a sensory evaluation of foods, be provided budget-friendly recipes and resources, and given take-home herbs, spices, and supporting materials
  • Be asked to complete 3-Day Food Records throughout the 6 week study period for assessment of dietary quality (4 total)
Read the detailed description

Study Overview: Investigators will recruit 30 college students experiencing poor dietary quality, to participate in this 6-week pilot, single-arm clinical trial. Participants will be recruited from the metropolitan Las Vegas area through campus and community advertisements including flyers, newspaper articles, social media, and public events. Randomization will not be needed as all participants recruited will be receiving the intervention. There will be two cohorts of 15 participants for the 6-week HSNP.

Prescreen Interview: Potential participants who inquire about the study by calling the recruitment phone line or by QR code via Qualtrics, will be given a brief overview of the study and will be asked a series of questions to determine whether they should be invited for the in-person screening visit. Eligibility will be based on inclusion/exclusion criteria and responses to questions about medical history and dietary habits. Potential participants will be invited to report to the clinical facilities in the Bigelow Health Sciences Building at UNLV (study site) for their first on-site visit (and all subsequent study visits if the participant qualifies) to ascertain eligibility (screening study visit). This pre-screening interview will occur prior to participants consenting (which occurs at the in person screening study visit).

Screening Study Visit: Potentially eligible participants will be invited to the Functional Foods and Health Lab (BHS313) of the Rod Lee Bigelow, Health Sciences Building at UNLV (health assessment-study site) for their first on-site visit for screening (and subsequent 2 study visits if the participant qualifies for the future Pre and Post-HSNP Visits) to ascertain eligibility. During this screening study visit, the potential participants will be provided with verbal and written explanations of the project and will have any questions regarding the study answered by trained research personnel during the informed consent process. Consenting participants will be asked to sign an informed consent document (with a copy provided to the participant to take home). Screening will consist of determination of dietary quality using the Rapid Prime Diet Quality Score Screener, SES Questionnaire, and an Herbs and Spices Questionnaire to determine usual herbs and spices intake. Anthropometrics and blood pressure will be measured and questions regarding medical history and medication use will be asked during the screening visit to confirm eligibility. Should the results of anthropometrics and/or blood pressure fall outside the range for inclusion, participants will be promptly notified and excluded from further participation before any additional data is collected. If participants meet the inclusion criteria for the study, they will be asked to come for subsequent study visits (Pre- and Post-HSNP Study Visits) and be a part of the 6-week HSNP Program. Participants who are not eligible will be thanked for their time and participation and told the specific reasoning for why they do not meet the inclusion criteria. Eligible participants will be asked to complete a three-day food record using NCI's Automated Self-Administered 24-Hour Dietary Assessment Tool to assess typical dietary intake and dietary quality (Healthy Eating Index [HEI]-2020 scoring), prior to their Pre-HSNP Study Visit at participants homes via a computer, ipad, or smartphone. The Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24) is a web-based dietary recall system developed by the National Cancer Institute. It allows participants to self-report their dietary intake over the past 24 hours using a user-friendly interface that prompts for detailed food and beverage consumption. The tool can be distributed via a unique web link provided to participants, enabling remote data collection without requiring in-person visits.

Fecal Sample Collection for Assessment of Gut Microbiome: After participants confirm eligibility from their screening visit, they will be given a "Fecal Collection Tube" with instructions provided. Participants will be asked to collect a sample in the privacy of your own home, to bring back with them to their Pre-HSNP Study Visit. Participants will prepare and collect a fecal sample using the provided tube. The collection tube cap will be unscrewed, and a small spoon will be provided to scoop one spoonful of feces. The fecal sample will then be placed in the collection tube. Finally, participants will tighten the cap and shake to mix the contents. The sample is fine to be stored at room temperature prior to bringing to BHS313 for the pre and post-HSNP Study Visits. Participants will also receive another Fecal Collection Tube at the end of their HSNP week-3 visit at the Nutrition Center to complete prior to coming in for their Post-HSNP Study visit, following all the same procedures as above.

Pre- and Post-HSNP Study Visit: Participants will be asked to come fasted to the study site (12 hours after the abstinence from caffeine and 24 hours after the last bout of moderate/heavy physical activity); vascular assessments (blood pressure, Pulse Wave Velocity, Pulse Wave Analysis) will be measured followed by body composition (Bioelectrical Impedance Analysis), finger prick blood draw (fasting blood glucose and lipid profiles, venous blood draw (inflammatory and oxidative stress biomarkers), anthropometrics (height, weight, and waist/hip circumference), assessment of fruit and vegetable intake via Raman Spectroscopy, assessment of physical activity patterns (Five-City Project Physical Activity Recall), nutrition knowledge (General Nutrition Knowledge Questionnaire), Mood State (Profile of Mood States Questionnaire), Gastrointestinal Health Questionnaires, and sleep quality (Pittsburg Sleep Quality Index).

Herbs and Spices Nutrition Education Program: Participants will visit the UNLV Nutrition Center for two visits after completion of their Pre-HSNP Study Visit at weeks 1 and 3 of the 6-week intervention to receive the HSNP in a group format (15 participants in each group), which our research team equipped with RD's has had experience creating and leading nutrition and education programs. HSNP will include an explanation of the principles and components of the Dietary Guidelines for Americans (DGA), health benefits of following the DGA, how to incorporate herbs and spices in the diet, guidance on recommended intake of various food groups, budget-friendly strategies and recipes for incorporation of herbs and spices in the diet, and supporting resources such as educational materials and online tools. Participants will then complete a sensory evaluation using the 9-point hedonic scale for various foods (including four different recipes for vegetables, fruits, grains/grain products, dairy products, and proteins/protein alternatives) prepared with various herbs and spices.

Dietary Assessments (4 three-day food records total) During Weeks 0 (Prior to Pre-HSNP Study Visit), 2, 4, and 6 of Intervention Period: Participants will be asked to complete a three-day food record using NCI's Automated Self-Administered 24-Hour (ASA24) Dietary Assessment Tool to assess typical dietary intake and diet quality (using HEI-202075) during weeks 0 (Prior to Pre-HSNP Study Visit), 2, 4, and 6 of the intervention period. This food record can be completed at any point during weeks 0 (Prior to Pre-HSNP Study Visit), 2, 4, and 6 of intervention the period at participants' homes via a computer or ipad.

Being tested
Herbs and Spices Nutrition Education Program
Keywords
dietary quality, dietary guidelines for americans, college students, cardiometabolic health, gut microbiome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Herbs and Spices Nutrition Education ProgramBehavioural

    Participants will attend two group visits at the UNLV Nutrition Center (weeks 0 and 3 of the 6-week intervention), where trained RDs will deliver the HSNP, covering the principles and health benefits of the Dietary Guidelines for Americans (DGA), recommended food group intake, and practical, budget-friendly strategies for incorporating herbs and spices into the diet. Sessions will include education, supporting materials, and a sensory evaluation of various foods (spanning fruits, vegetables, grains, dairy, and proteins) prepared with various herbs and spices, rated using a 9-point hedonic scale to identify preferred flavor profiles and promote long-term DGA adherence through enhanced taste and acceptability.

Study groups in NCT07082348
Study groupRoleWhat they receive
Herbs and Spices Nutrition Education ProgramExperimentalParticipants will attend two group visits at the UNLV Nutrition Center (weeks 0 and 3 of the 6-week intervention), where trained RDs will deliver the HSNP, covering the principles and health benefits of the Dietary Guidelines for Americans (DGA), recommended food group intake, and practical, budget-friendly strategies for incorporating herbs and spices into the diet. Sessions will include education, supporting materials, and a sensory evaluation of various foods (spanning fruits, vegetables, grains, dairy, and proteins) prepared with various herbs and spices, rated using a 9-point hedonic scale to identify preferred flavor profiles and promote long-term DGA adherence through enhanced taste and acceptability.
Receives: Behavioral: Herbs and Spices Nutrition Education Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in Dietary Quality

    Dietary Quality measured via Health Eating Index-2020 from three-day food records using NCI's Automated Self-Administered 24-Hour Dietary Assessment Tool. The index score will be from 0-100, with 0 indicating poorest diet quality and 100 excellent.

    Measured: Weeks 0 (Prior to Pre-HSNP,) 2, 4 and 6 of intervention period: 6 weeks

  2. Changes In Dietary Intake

    Dietary intake measured from three-day food records using NCI's Automated Self-Administered 24-Hour Dietary Assessment Tool, will be measured throughout the study period to indicate any changes in overall macro and micro nutrient intake between the treatment and comparative control group.

    Measured: Weeks 0 (Prior to Pre-HSNP,) 2, 4 and 6 of intervention period: 6 weeks

  3. Feasibility of HSNP

    To recruit at least 80% of the target sample size (24 out of 30 participants), retain at least 85% of enrolled participants through to the end HSNP (no more than 4 dropouts), deliver ≥90% of planned HSNP intervention, and collect ≥90% of three-day food records through the study period.

    Measured: Throughout Intervention Period: 6 weeks

  4. Adherence of HSNP

    To have ≥80% of participants completing the whole HSNP (attending both study visits and nutrition education sessions; 24 out of 30 participants)

    Measured: Weeks 1 and 3 of intervention period: 6 weeks

  5. Acceptability of HSNP

    To asses acceptability at the 3-week HSNP visit and upon completing of HSNP via survey and optional semi-structured interviews. The survey will include Likert-Scale items (1-5 and 1-10) across satisfaction, perceived relevance, taste, convenience, and likelihood of continued use.

    Measured: Week 3 and Post- HSNP Study Visit: 6 weeks

Secondary outcomes (26)
  1. Change in Fasting Blood Glucose Levels

    Fasting Blood Glucose Levels Measured with a Glucometer

    Measured: Pre- and Post- HSNP: 6 weeks

  2. Change in Lipid Profiles

    Measure of fasted lipid profiles (total cholesterol, triglycerides, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol) all measured in milligrams per deciliter (mg/dL) via Cholestech LDX Analyzer

    Measured: Pre- and Post-HSNP: 6 weeks

  3. Change in Blood Pressure

    Fasted diastolic and systolic blood pressure, measured via OMRON automated blood pressure device

    Measured: Pre- and Post-HSNP: 6 weeks

  4. Changes in Arterial Stiffness-Pulse Wave Velocity

    Fasted measured of arterial stiffness via carotid-femoral and aortic pulse wave velocity (cfPWV) in meters per second (m/s) (SphygmoCor XCEL).

    Measured: Pre- and Post-HSNP: 6 weeks

  5. Changes in Arterial Stiffness-Augmentation Index

    Fasted measured of arterial stiffness via pulse wave analysis (SphygmoCor XCEL) with measure of Augmentation Index (AIx) expressed as a percentage (%)

    Measured: Pre- and Post-HSNP: 6 weeks

  6. Changes in Arterial Stiffness- Central Systolic Blood Pressure

    Fasted measured of Central Systolic Blood Pressure (cSBP) measured in mmHg (millimeters of mercury) via SphygmoCor XCEL.

    Measured: Pre- and Post- HSNP: 6 weeks

  7. Changes in Arterial Stiffness-Central Pulse Pressure

    Fasted measured of Central Pulse Pressure measured in mmHg (millimeters of mercury) via SphygmoCor XCEL.

    Measured: Pre- and Post-HSNP: 6 weeks

  8. Changes in Arterial Stiffness-Augmented Pressure

    Fasted measured of Augmented Pressure measured in mmHg (millimeters of mercury) via SphygmoCor XCEL

    Measured: Pre- and Post-HSNP: 6 weeks

  9. Changes in Arterial Stiffness-Subendocardial Viability Ratio

    Fasted measured of arterial stiffness via pulse wave analysis (SphygmoCor XCEL) with measure of Subendocardial Viability Ratio expressed as a percentage (%)

    Measured: Pre- and Post- HSNP: 6 weeks

  10. Changes In Arterial Stiffness-Transit Time

    Fasted measured of arterial stiffness via transit in milliseconds (SphygmoCor XCEL)

    Measured: Pre- and Post-HSNP: 6 weeks

  11. Changes in waist and hip circumferences

    Waist and hip circumference changes measured in centimeters.

    Measured: Pre- and Post- HSNP: 6 weeks

  12. Change in body fat %

    Body fat % measured via Bioelectrical Impedance Analysis (Seca BIA Platform mBCA 554 Medical Body Composition Analyzer)

    Measured: Pre- and Post- HSNP: 6 weeks

  13. Changes in Nutrition Knowledge

    Measurements of nutrition knowledge via General Nutrition Knowledge Questionnaire which are general questions used to assess a person's understanding of basic nutrition principles and dietary guidelines.

    Measured: Pre- and Post- HSNP: 6 weeks

  14. Changes in Fruit and Vegetable Intake Adherence

    Assessment of fruit and vegetable intake will be measured via Raman Spectroscopy (VeggieMeter)

    Measured: Pre- and Post HSNP: 6 weeks

  15. Changes in Physical Activity Patterns

    Assessment of physical activity patterns via Five-City Project Physical Activity Recal

    Measured: Pre- and Post- HSNP: 6 weeks

  16. Changes in Sleep Quality

    Assessment of sleep quality measured via Pittsburg Sleep Quality Index wich is a questionnaire used to assess the quality and patterns of sleep over a one-month period, measuring factors like sleep duration, sleep disturbances, and daytime dysfunction. The scores are typically presented as a global score, ranging from 0 to 21, where higher scores indicate poorer sleep quality.

    Measured: Pre- and Post- HSNP: 6 weeks

  17. Changes in body weight

    Body weight will be measured in kilograms with a weighing scale

    Measured: Pre- and Post- HSNP: 6 weeks

  18. Changes in Body Mass Index

    Body Mass Index will be assessed with a participants height in meters and body weight in kilograms, in the unit of kg/m2

    Measured: Pre- and Post- HSNP: 6 weeks

  19. Assessment of Height

    Height will be assessed in meters (for assessment of BMI at future visits and inclusion criteria)

    Measured: Screening

  20. Changes in High Sensitive C-Reactive Protein

    Fasted measure of plasma high sensitivity C-Reactive Protein in mg/L measured via ELISA

    Measured: Pre- and Post- HSNP: 6 weeks

  21. Changes in Interleukin-6

    Fasted measure of plasma Interleukin-6 in pg/mL measured via ELISA

    Measured: Pre- and Post-HSNP: 6 weeks

  22. Change in Oxidized-LDL

    Fasted plasma oxidized LDL (U/L) will be measured via ELISA

    Measured: Pre- and Post-HSNP: 6 weeks

  23. Change in Lipopolysaccharide Binding Protein

    Fasted measure of plasma Lipopolysaccharide Binding Protein in ng/mL measured via ELISA

    Measured: Pre- and Post- HSNP: 6 weeks

  24. Changes in Gut Microbiome

    Fecal sample collection of Alpha and Beta Diversity from 16S rRNA

    Measured: Pre- and Post- HSNP: 6 weeks

  25. Changes in Gastrointestinal Health

    To measure the presence, frequency, history and severity of digestive symptoms such as bloating, gas, abdominal pain, diarrhea, constipation, and overall gut discomfort.

    Measured: Pre- and Post- HSNP: 6 weeks

  26. Changes in Mood (Profile of Mood States Questionnaire)

    Measure of an individuals current mood across several emotional states, including tension, depression, anger, fatigue, confusion, and vigor.

    Measured: Pre- and Post- HSNP: 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jul 2025
  2. Study start3 Jul 2025
  3. Primary completion6 Apr 2026
  4. Study completion6 Apr 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07082348
Sponsor's protocol ID
UNLV-2024-569
Acronym
HerbSpicesDiet
Status last verified
Jun 2025
First submitted
11 Jun 2025
Last updated
7 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual Participant Data (IPD) will not be shared because the study did not obtain participant consent for data sharing, and there are concerns regarding the protection of participant privacy and confidentiality. Additionally, institutional and regulatory policies restrict data sharing, and the data are not intended for broader dissemination.

Questions about this trial

What is this clinical trial studying?

A study testing Herbs and Spices Nutrition Education Program in people with Dietary Quality and Feasibility Studies, run by University of Nevada, Las Vegas at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in Dietary Quality (time frame: Weeks 0 (Prior to Pre-HSNP,) 2, 4 and 6 of intervention period: 6 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.

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