Body Composition

41

Review clinical trials related to Body Composition. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Body Roundness Index and Mortality in ICU Patients

This study investigates whether Body Roundness Index (BRI), an anthropometric measure derived from waist circumference and height, can predict mortality in adult intensive care unit (ICU) patients. BRI captures central adiposity and body fat distribution more accurately than Body Mass Index (BMI). In this prospective multicenter cohort study, BRI will be measured at ICU admission and its association with ICU mortality, 28-day mortality, hospital mortality, mechanical ventilation duration, ICU length of stay, and acute kidney injury will be evaluated. The predictive performance of BRI will also be compared with BMI.

Participants needed: 550
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ondokuz Mayıs UniversityUpdated: Jun 8, 2026Locations: 1Duration: 28 Days
Eligibility criteria

Age ≥18 years [+2]

Age <18 years [+4]

Status: Recruiting

Effects of Blood Flow Restriction Training on Body Composition and Maximal Strength in Military Personnel

This study aims to compare the effects of low-intensity blood flow restriction training combined with resistance training versus traditional high-intensity resistance training on body composition (skeletal muscle mass, body fat mass) and maximal strength (isometric mid-thigh pull, vertical jump, isometric squat pull) in male military academy cadets. The study lasts for 6 weeks and adopts a randomized parallel-group design.

Participants needed: 36
Trial details
Biological sex: AllType: InterventionalSponsor: Yang LiuUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Male cadets from military academy; [+3]

Major sports injury within 2 years (fracture, ligament tear, muscle/tendon ruptu... [+2]

Status: Recruiting

Role of Body Composition in Large for Gestational Age Infants (LGA) With Oral Feeding Difficulty

Large for Gestational Age (LGA) infants have excess fat-mass (FM) proportion secondary to prolonged in utero exposure to an energy-rich environment. Our preliminary data suggest that excess FM proportion can be associated with oral feeding delay and a potentially modifiable therapeutic target to improve oral feeding outcomes. The objective of this study is to determine the impact of a short-term Fat-free mass (FFM)-indexed feeding on the oral intake volumes in LGA infants with oral feeding difficulties.

Participants needed: 40
Trial details
Age: 1-10Biological sex: AllType: InterventionalSponsor: Nemours Children's ClinicUpdated: May 27, 2026Locations: 2
Eligibility criteria

LGA infants with oral feeding difficulty born at ≥ 35 weeks gestation, with FM z...

Infants on any respiratory support, Infants on enteral feeding duration > 60 min...

Status: Not yet recruiting

Lifestyle Intervention to Improve Muscle Function in Older Adults

The goal of this randomized controlled two-arm trial is to determine the effect of a diet and exercise intervention for 12 weeks on body composition, muscle function, and energy balance in 80 adults aged 50 years and over with obesity and insulin resistance. The main questions the trial aims to answer are: Will 12 weeks of a structured nutrition plan + exercise reduce fat mass, improve muscle function, and increase energy deficit compared to the usual diet + exercise. The hypothesis is that 12 weeks of a structured nutrition plan + exercise will reduce fat mass, improve muscle function, and produce greater energy deficit than the usual diet + exercise. Participants will be provided with all meals for 12 weeks and will exercise at the Center under supervision three times each week. Pre and post-intervention, body composition, physical function, and energy deficit will be measured.

Participants needed: 80
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Pennington Biomedical Research CenterUpdated: May 22, 2026Locations: 1
Eligibility criteria

Age > 50 years. [+6]

Diagnosis of cancer (received within five years) or diabetes (type 1 and 2), or... [+3]

Status: Not yet recruiting

Validation of a Body-Composition Segmentation Software on a Diverse Public CT Scan Cohort

This study evaluates the standalone performance of Soma, a deep-learning software developed by Nucleo Research, Inc. for the automated segmentation of body-composition tissues (skeletal muscle, subcutaneous adipose tissue, visceral adipose tissue, and intramuscular adipose tissue) on whole-body computed tomography (CT) images. The aim is to confirm that Soma produces segmentations and tissue-area measurements that agree with a multi-rater expert reference standard, on a diverse cohort representative of demographic and clinical variation. A total of 200 CT scans are sampled by stratified design from a curated pool of 2,066 scans aggregated from six publicly available, de-identified imaging datasets (autoPET, AMOS, MSD Pancreas, CT-ORG, ENHANCE.PET, RATIC). Three board-certified radiologists independently annotate the reference standard at the L3 slice. Primary performance is assessed using the Dice similarity coefficient against the multi-rater reference, with predefined thresholds and BCa bootstrap confidence intervals, both in aggregate and within every demographic and clinical subgroup. Secondary endpoints include Bland-Altman analysis of tissue-area agreement, 95th-percentile Hausdorff distance, Pearson correlation of derived indices, and Cohen's kappa for sarcopenia classification using Skeletal Muscle Index (SMI). The study is fully retrospective on de-identified images, involves no patient contact, and has been determined exempt by Salus IRB (Salus Number 26328) under 45 CFR 46.104(d)(4).

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Nucleo Research, Inc.Updated: May 22, 2026Locations: 1
Eligibility criteria

Subjects above 16 years or older at the time the source imaging was acquired. [+3]

Subject under 16 years of age at the time the source imaging was acquired. [+3]

Status: Not yet recruiting

Mediterranean Diet Uptake and Nutrition on Child Health, Inflammation, and Early-life Symbiosis (MUNCHIES) Study

Toddlerhood (ages 2-3) is a critical window when the gut microbiome is still developing and eating habits are being established. Yet, many Canadian toddlers eat diets high in sugar and salt, which may affect long-term health. This study will test whether a MED diet can improve dietary inflammation, gut health, and body composition in toddlers and whether a tailored nutrition education program for parents can help families maintain healthy eating patterns. In this study, toddlers will be randomly assigned to a 3-week MED diet or their usual diet. Families in the MED diet group will receive free meal boxes for the 3 weeks, plus guidance from a nutrition researcher through a structured education program. The standard diet group will continue their regular diet with general nutrition advice. Researchers will collect dietary information, body composition assessments, and stool samples to measure gut microbiome composition and metabolites. This first study of a controlled diet intervention in toddlers, combining behavioral support, high-quality food provision, and advanced gut microbiome analysis, will help understand how early diet shapes lifelong eating habits and health, guiding public health strategies and precision nutrition approaches to prevent chronic disease from early life.

Participants needed: 40
Trial details
Age: 24-36Biological sex: AllType: InterventionalSponsor: University of New BrunswickUpdated: May 12, 2026Locations: 1
Eligibility criteria

Parent is ≥19 years of age. [+9]

Toddler has food allergies or dietary restrictions (e.g., gluten-free) that make... [+6]

Status: Not yet recruiting

Effects of 8-Week CrossFit-Based Concurrent Training on Fitness, Body Composition, and Psychological Outcomes in Schoolchildren

This study examines the effects of an 8-week CrossFit-based concurrent training program in boys and girls aged 7 to 11 years, comparing an experimental group (n=15) with a control group (n=15). The aim is to assess changes in strength, cardiorespiratory fitness, body composition, and psychological variables such as anxiety, stress, and self-esteem, using field-based physical tests (CMJ, Course Navette, handgrip strength, etc.) and validated questionnaires. The study follows a randomized controlled trial design with pre- and post-intervention assessments. The experimental group will complete two weekly CrossFit sessions adapted for children, while the control group will maintain their usual routine without structured physical training. The hypothesis states that the intervention will significantly improve both physical performance and psychological well-being in the experimental group compared to the control group.

Participants needed: 30
Trial details
Age: 7-11Biological sex: AllType: InterventionalSponsor: Maimónides Biomedical Research Institute of CórdobaUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Age: 7-11 years. [+4]

Children with musculoskeletal injuries, diseases, or medical, psychological, or... [+2]

Status: Recruiting

The Synergistic Effects of Menopause and HIV on Cardiovascular Disease Risk in Women

Menopause is associated with the acceleration of many comorbidities, including cardiovascular disease. Whether HIV and menopause together increase cardiovascular disease risk is a key knowledge gap. The goal of this observational study is to address this knowledge gap by looking at the role of menopause on cardiovascular disease risk factors such as insulin resistance, hypertension, hyperlipidemia, and carotid atherosclerosis using previously collected data. The investigators will look at underlying causes for cardiovascular diseases worsening in menopausal women with HIV by looking at the role of increased inflammation in the body and whether this is altered by weight. The investigators achieve this by enrolling participants who are willing to undergo a whole body MRI.

Participants needed: 90
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: University of California, San FranciscoUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

90 non-pregnant women with HIV (approximately 30 in each menopausal phase) from...

Women who are not virally suppressed (HIV RNA >200 copies/mL) [+3]

Status: Recruiting

Dose-Response Impact of Geranylgeraniol (GG) Supplementation on Muscle Health

This study will evaluate the effects of daily geranylgeraniol (GG) supplementation on muscular strength, body composition, and aerobic capacity in healthy, physically active men and women. Approximately 60 participants aged 30-60 years will be enrolled in a randomized, double-blind, placebo-controlled, parallel-group trial lasting 8 weeks. Participants will be assigned to receive either placebo, 150 mg GG, or 300 mg GG daily. Outcome measures will be assessed at baseline, week 4, and week 8 and include maximal strength (1RM bench press and leg press), fat-free mass, muscular endurance, aerobic capacity (VO2peak), and circulating biomarkers related to metabolism and health.

Participants needed: 70
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: Lindenwood UniversityUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

Between 30 and 60 years old. [+7]

BMI <18.5 or > 29.9 kg/m2 [+21]

Status: Recruiting

Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Prediabetes

The goal of this clinical trial is to determine the effectiveness of using a freeze-dried wild blueberry powder on cardiometabolic health, cognitive function, and gut microbiota composition in adult women with prediabetes.

Participants needed: 30
Trial details
Age: 20-65Biological sex: FemaleType: InterventionalSponsor: Georgia State UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Women aged 20-65 years old [+2]

Allergies to berries [+8]

Status: Recruiting

EMS Combined With Resistance Training in Weight Lifters

The purpose of this randomized controlled trial is to determine the effects of Electrical Muscle Stimulation (EMS) combined with resistance training on muscle mass, muscular strength, body composition, and power in trained weightlifters. Participants will be randomly allocated into two groups: one receiving resistance training alone and the other receiving EMS combined with resistance training. The intervention will be conducted for eight weeks, and outcome measures will be assessed at baseline, mid-intervention (4 weeks), and post-intervention (8 weeks). The findings of this study may provide evidence regarding the additional benefits of EMS when combined with conventional resistance training programs in enhancing muscular performance among trained athletes.

Participants needed: 34
Trial details
Age: 18-40Biological sex: MaleType: InterventionalSponsor: Riphah International UniversityUpdated: Mar 20, 2026Locations: 1
Eligibility criteria

Male participants aged 18-40 years [+3]

Neuromuscular disorders [+3]

Status: Recruiting

Longitudinal Body Composition Assessment in Breast Cancer Patients

This observational cohort study aims to track longitudinal changes in body composition, including skeletal muscle mass and fat distribution, in patients diagnosed with breast cancer. Following primary surgery and adjuvant therapy, participants will be monitored over a 2-year period. The primary objective is to evaluate the natural progression of skeletal muscle mass index (SMI) and metabolic changes in this population. By conducting serial measurements, this study seeks to characterize the longitudinal trends in muscle loss and body composition shifts post-treatment, providing data to better understand the physiological impact of the cancer recovery process.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical FoundationUpdated: Mar 16, 2026Locations: 1Duration: 12 Months
Eligibility criteria

>18 years of age [+2]

Women diagnosed with metastatic (stage IV) breast cancer [+3]

Status: Recruiting

Body Composition and Lifestyles in Athletes With Disabilities

Disability involves limitations that affect mobility and the ability to perform daily activities and achieve competitive goals. It is expected that disability has a significant impact on body composition, including reductions in lean mass and bone mineral content, and increases in fat mass and its distribution. Additionally, the assessment of food and dietary supplement intake among athletes with disabilities remains poorly described, despite its relevance in both sports and health contexts due to the potential benefits of individualized nutritional strategies. This research project, entitled Anthropometric, Dietary, Exercise, and Supplementation Profile in Athletes with Disabilities (PADES), aims to describe the anthropometric characteristics, physical exercise practices, and food and supplement intake in Spanish athletes with disabilities. The study seeks to address the current lack of standardized anthropometric data and the limited information on dietary and supplementation patterns in this population, which hinders a comprehensive understanding of the physiological, nutritional, and biomechanical aspects essential for their health and athletic performance. A cross-sectional, descriptive-correlational study will be conducted in Spanish athletes with disabilities recruited through the Spanish Federation of Sports for People with Physical Disabilities (FEDDF), the Spanish Federation of Sports for the Blind (FEDC), and the Spanish Federation of Sports for the Deaf (FEDS).

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of AlicanteUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Acceptation of informed consent [+4]

No attendance to the evaluations [+1]

Status: Not yet recruiting

Breastmilk and the Link to Overweight/Obesity and Maternal Diet in the Mother-breastmilk-child Triad

The prospective 5-month follow-up study will involve 150 mother-infant dyads grouped based on maternal baseline BMI category (normal weight, overweight, obesity). The investigators plan 3 study visits (1, 3, and 6 months postpartum) with analysis the following parameters and outcomes: 1. maternal anthropometry and body composition; 2. maternal dietary intake and dietary patterns (with results of biomarker-based validation); 3. maternal status of lipophilic antioxidants, selected vitamins, and fatty acids profile that may be related to adipose tissue metabolism, inflammation, and cardiometabolic status; 4. maternal metabolomics, adipokines, insulin, selected biomarkers of inflammation, altered glucose metabolism, and oxidation; 5. breastmilk composition assessed by systemic approach (macronutrients, fatty acids profile, lipophilic antioxidants, adipokines, hormones, immunological profile, and preliminary lipidomic analysis in part of the study group); 6. infant growth trajectory, body composition, urine metabolomics, and biomarkers of oxidative stress. Additionally, maternal and infant stool, buccal swabs, and human milk samples will be banked for further microbiome analysis studies.

Participants needed: 165
Trial details
Age: 19+Biological sex: FemaleType: ObservationalSponsor: Warsaw University of Life SciencesUpdated: Mar 9, 2026Locations: 4
Eligibility criteria

at least 19 years, [+6]

type 1 or 2 diabetes diagnosed before pregnancy, [+6]

Status: Not yet recruiting

CT Body Composition as Predictor of Exercise Therapy Outcome in Peripheral Arterial Disease

Supervised exercise therapy (SET) is the recommended first treatment for patients with leg artery disease (peripheral arterial disease, PAD) causing pain when walking. However, approximately 40% of patients do not benefit meaningfully and go on to require a procedure to open the blocked arteries within three months. This study investigates whether body composition measurements - specifically the quality of muscle and the amount of belly fat - taken from a CT scan already performed as part of routine care, can identify before treatment begins which patients are unlikely to respond to exercise therapy. If confirmed, this approach would allow doctors to use information from a scan patients are already having, with no additional tests, to better match patients to the right treatment from the start.

Participants needed: 128
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Nemocnice AGEL Trinec-Podlesi a.s.Updated: Feb 25, 2026
Eligibility criteria

Age 18 years or older [+5]

Fontaine stage III or IV peripheral arterial disease (rest pain or tissue loss;... [+5]

Status: Recruiting

Impact of Supplementation in Improving Metabolic Health Outcomes (ISMOS) Study

This study investigates the role of multivitamin and multimineral (MVM) supplementation in improving metabolic, musculoskeletal, and mental health among midlife Asian women aged 40-60 years, a critical period marked by hormonal and physiological transitions from pre- to post-menopause. Evidence from the GUSTO cohort in Singapore has shown that higher plasma levels of vitamins B6, B9, B12, and D are associated with better metabolic profiles, insulin sensitivity, and mental wellbeing, while deficiencies are linked to increased metabolic and psychological risks. Given that vitamin insufficiency and central obesity are highly prevalent among Asian women even at lower BMI, this randomized, double-blind, placebo-controlled trial will evaluate whether 12 months of daily MVM supplementation can reduce MetaboAge and improve metabolic, mental, and muscle health outcomes compared with placebo. Findings will inform preventive strategies for extending health span and mitigating chronic disease risks among midlife women in Asia.

Participants needed: 400
Trial details
Age: 40-60Biological sex: FemaleType: InterventionalSponsor: Institute for Human Development and Potential (IHDP), SingaporeUpdated: Feb 25, 2026Locations: 1
Eligibility criteria

Women aged 40-60 years old [+4]

Pregnant or planning a pregnancy [+9]

Status: Recruiting

GLP-1RA Effects on Lean Mass and Bone Health in Midlife Women

This study is designed with the interest to learn on the effects of estrogen levels and how it affects body compositions and muscle function in midlife women who are taking a GLP-1RA for weight loss.

Participants needed: 50
Trial details
Age: 35-60Biological sex: FemaleType: ObservationalSponsor: University of Kansas Medical CenterUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Females [+5]

Pregnant women [+8]

Status: Recruiting

The Association Between Core Temperature and Health

The goal of this clinical trial is to learn if cold water drinking could promote body composition and further extend healthy lifespan in Chinese older adults. The main questions it aims to answer are: 1. Does cold water drinking lower the body fat percentage? 2. Will cold water drinking positively extend lifespan in a long-term Researchers will compare cold water intervention group to a control group (drinking 37℃ water instead) to see if cold water drinking works to promote health and slow down ageing process. Participants will: 1. Drink 4℃ or 37℃ water 4 times (9a.m., 12p.m., 15p.m., 18p.m.) every day for 6 months. 2. Visit the institute and health checkup department for tests and checkup at baseline, the end of the 3rd month, and the end of 6th month.

Participants needed: 36
Trial details
Age: 50-65Biological sex: AllType: InterventionalSponsor: Shenzhen Institutes of Advanced Technology ,Chinese Academy of SciencesUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

Aged between 50 and 65 years old (including 50 and 65) [+4]

Those who need to take medication for a long term (including diet pills) [+7]

Status: Not yet recruiting

Open Space and Closed Years

The primary objective of this project is to examine the effects of a specific multicomponent physical activity program (MPAP), conducted in an outdoor setting, on the health and functional-motor status (HFMS) of women over the age of 60. Additionally, the study will investigate the influence of sociodemographic factors (SDF), physical literacy (PL), and health literacy (HL) on the baseline HFMS and the subsequent changes resulting from the KTP. Study Methodology The program participants will consist of older women (\>60 years; n=60) whose current HFMS allows for participation in the exercise protocol. They will be divided into two groups: Experimental Group: Will participate in the MPAP. Control Group: Will not participate in the MPAP. The exercise intervention (MPAP) will include a combination of aerobic activities, strength exercises, balance, and flexibility. It will be conducted two to three times per week across two three-month cycles, separated by a three-month break. Data Collection and Environment Assessments: Sociodemographic factors, physical literacy, and health literacy will be measured at the start of the study. A series of HFMS indicators will be recorded before and after each exercise cycle. Setting: The MPAP will be performed outdoors in a public park. Project Significance Beyond analyzing the direct effects of the exercise program and the correlations between the measured variables, this project will contribute to a deeper understanding of the importance of the natural environment in implementing goal-oriented physical activity for the elderly population.

Participants needed: 150
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Goran KuvacicUpdated: Jan 26, 2026
Eligibility criteria

physical fitness status which allows active participation in the physical exerci...

health conditions not allowing the participation in treatment program

Status: Recruiting

Body Composition and Exercise to Prevent Muscle Loss With GLP1 Agonist Treatment

The goal of this study is to learn if a smartwatch that measures activity level and body composition, combined with exercise reminders, can safely improve strength and muscle mass in people who recently started or are planning to start treatment with incretin therapy (liraglutide, semaglutide, tirzepatide or retatrutide), also known as glucagon-like peptide 1 receptor agonist (GLP-1 RA) medications.

Participants needed: 100
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years old at time of signing informed consent [+2]

Current pregnancy (positive urine hCG) or plans to become pregnant in the next 6... [+4]

Status: Recruiting

How Does Continued Use of Green Light Therapy Impact Outcomes?

Already using Green Light Therapy? Explore how continued use with twice-weekly 20-minute sessions may continue to support positive changes in body composition. Discover whether this non-invasive wellness approach gets better over time to help support energy, balance, and renewal.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Efforia, IncUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Can read and understand English. [+2]

Individuals with eye conditions [+1]

Status: Recruiting

Can EmeraldLED Reshape Your Body With Continued Use?

Already using EmeraldLED? TheGreen Light Therapy study explores how continuing participants' 15-minute sessions, twice a week, may continue to support positive changes in body composition.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Efforia, IncUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Can read and understand English. [+2]

Individuals with eye conditions [+1]

Status: Recruiting

Discover Better Body Composition With Green Light!

Investigation into Green Light Therapy study using EmeraldLED for 15-minute sessions, twice a week, to support positive changes in body composition.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Efforia, IncUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Can read and understand English. [+2]

Status: Recruiting

Dietary Patterns, Inflammation, Zinc Status, and Body Composition in Multi-Ethnic Women of Reproductive Age in Jakarta

This study aims to determine the relationship between dietary patterns and hair zinc levels with body composition, tumor necrosis factor alpha (TNF-α), and blood pressure in women of reproductive age from different ethnic backgrounds in Jakarta, Indonesia (specifically Minangkabau, Sundanese, Javanese, Betawi, and Chinese). Participants are assessed once through dietary assessment, anthropometric measurements, and biological sample collection.

Participants needed: 188
Trial details
Age: 19-49Biological sex: FemaleType: ObservationalSponsor: Indonesia UniversityUpdated: Dec 4, 2025Locations: 1
Eligibility criteria

Women aged 19-49 years [+4]

History of chronic diseases (e.g., diabetes, cardiovascular disease, cancer) [+2]

Status: Recruiting

Feasibility and Potential Efficacy of Herbs and Spices for Improving Dietary Quality in College Students: 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? 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 (one week prior 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 0 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)

Participants needed: 30
Trial details
Age: 18-39Biological sex: AllType: InterventionalSponsor: University of Nevada, Las VegasUpdated: Nov 24, 2025Locations: 1
Eligibility criteria

College students (undergraduate and graduate) [+4]

Individuals diagnosed with myocardial infarction within the past 6 months [+16]