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.
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
- Conditions the study is for
- Dietary Quality, Feasibility Studies, College Student
- What is being tested?
- Herbs and Spices Nutrition Education Program
- Type of treatment
- Lifestyle or therapy programme
- 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
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.
- Conditions
- Dietary Quality, Feasibility Studies, College Student, Dietary Guidelines for Americans, Gut Microbiome, Lipid Profiles
- 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 group | Role | What they receive |
|---|---|---|
| Herbs and Spices Nutrition Education Program | Experimental | 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. 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.
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
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
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
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
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)
Change in Fasting Blood Glucose Levels
Fasting Blood Glucose Levels Measured with a Glucometer
Measured: Pre- and Post- HSNP: 6 weeks
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
Change in Blood Pressure
Fasted diastolic and systolic blood pressure, measured via OMRON automated blood pressure device
Measured: Pre- and Post-HSNP: 6 weeks
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
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
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
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
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
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
Changes In Arterial Stiffness-Transit Time
Fasted measured of arterial stiffness via transit in milliseconds (SphygmoCor XCEL)
Measured: Pre- and Post-HSNP: 6 weeks
Changes in waist and hip circumferences
Waist and hip circumference changes measured in centimeters.
Measured: Pre- and Post- HSNP: 6 weeks
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
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
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
Changes in Physical Activity Patterns
Assessment of physical activity patterns via Five-City Project Physical Activity Recal
Measured: Pre- and Post- HSNP: 6 weeks
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
Changes in body weight
Body weight will be measured in kilograms with a weighing scale
Measured: Pre- and Post- HSNP: 6 weeks
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
Assessment of Height
Height will be assessed in meters (for assessment of BMI at future visits and inclusion criteria)
Measured: Screening
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
Changes in Interleukin-6
Fasted measure of plasma Interleukin-6 in pg/mL measured via ELISA
Measured: Pre- and Post-HSNP: 6 weeks
Change in Oxidized-LDL
Fasted plasma oxidized LDL (U/L) will be measured via ELISA
Measured: Pre- and Post-HSNP: 6 weeks
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
Changes in Gut Microbiome
Fecal sample collection of Alpha and Beta Diversity from 16S rRNA
Measured: Pre- and Post- HSNP: 6 weeks
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
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.
- First posted24 Jul 2025
- Study start3 Jul 2025
- Primary completion6 Apr 2026
- Study completion6 Apr 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dietary QualityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Nevada, Las Vegas
- Sponsor type
- University, hospital or other
- Collaborators
- McCormick Science Institute
- Responsible party
- Sponsor
- Investigators
- Neda S Akhavan, PhD, RD, Principal investigator, University of Nevada, Las Vegas
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.
Study at a glance
From the registry record, last updated by the sponsor on 7 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT07082348
- Acronym / sponsor ID
- HerbSpicesDiet / UNLV-2024-569
- Conditions
- Dietary Quality, Feasibility Studies, College Student, Dietary Guidelines for Americans, Gut Microbiome, Lipid Profiles
- Keywords
- dietary quality, dietary guidelines for americans, college students, cardiometabolic health, gut microbiome
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- University of Nevada, Las VegasUniversity, hospital or other
- Collaborators
- McCormick Science Institute
- Study start
- 3 Jul 2025 (actual)
- Primary completion
- 6 Apr 2026 (actual)
- Study completion
- 6 Apr 2026 (actual)
- First posted
- 24 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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?
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)
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Herbs and Spices Nutrition Education Program | Experimental | Behavioral: Herbs and Spices Nutrition Education ProgramParticipants 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. |
Who may qualify
- Ages
- 18 to 39 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- 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.
Key exclusion criteria (17 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Herbs and Spices Nutrition Education ProgramParticipants 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. | Behavioural | Herbs and Spices Nutrition Education Program |
Primary outcome
Changes in Dietary Quality
Time frame: Weeks 0 (Prior to Pre-HSNP,) 2, 4 and 6 of intervention period: 6 weeks
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.
Changes In Dietary Intake
Time frame: Weeks 0 (Prior to Pre-HSNP,) 2, 4 and 6 of intervention period: 6 weeks
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.
Feasibility of HSNP
Time frame: Throughout Intervention Period: 6 weeks
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.
Adherence of HSNP
Time frame: Weeks 1 and 3 of intervention period: 6 weeks
To have ≥80% of participants completing the whole HSNP (attending both study visits and nutrition education sessions; 24 out of 30 participants)
Acceptability of HSNP
Time frame: Week 3 and Post- HSNP Study Visit: 6 weeks
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.
26 secondary outcomes
Change in Fasting Blood Glucose Levels
Time frame: Pre- and Post- HSNP: 6 weeks
Change in Lipid Profiles
Time frame: Pre- and Post-HSNP: 6 weeks
Change in Blood Pressure
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in Arterial Stiffness-Pulse Wave Velocity
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in Arterial Stiffness-Augmentation Index
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in Arterial Stiffness- Central Systolic Blood Pressure
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Arterial Stiffness-Central Pulse Pressure
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in Arterial Stiffness-Augmented Pressure
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in Arterial Stiffness-Subendocardial Viability Ratio
Time frame: Pre- and Post- HSNP: 6 weeks
Changes In Arterial Stiffness-Transit Time
Time frame: Pre- and Post-HSNP: 6 weeks
Changes in waist and hip circumferences
Time frame: Pre- and Post- HSNP: 6 weeks
Change in body fat %
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Nutrition Knowledge
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Fruit and Vegetable Intake Adherence
Time frame: Pre- and Post HSNP: 6 weeks
Changes in Physical Activity Patterns
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Sleep Quality
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in body weight
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Body Mass Index
Time frame: Pre- and Post- HSNP: 6 weeks
Assessment of Height
Time frame: Screening
Changes in High Sensitive C-Reactive Protein
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Interleukin-6
Time frame: Pre- and Post-HSNP: 6 weeks
Change in Oxidized-LDL
Time frame: Pre- and Post-HSNP: 6 weeks
Change in Lipopolysaccharide Binding Protein
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Gut Microbiome
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Gastrointestinal Health
Time frame: Pre- and Post- HSNP: 6 weeks
Changes in Mood (Profile of Mood States Questionnaire)
Time frame: Pre- and Post- HSNP: 6 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Oct 2026.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Neda S Akhavan, PhD, RD principal investigator
University of Nevada, Las Vegas
1 site in 1 country: see every site and its status.
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.