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Food and Fitness With Medicine (FFWM) 200 Biomarker-Driven Randomized

Recruiting
Clinical Trial NCT07027995 (FFWM) is an interventional study for Cardiovascular Kidney Metabolic Syndrome, Type 2 Diabetes that is recruiting. It started on January 14, 2026 with plans to enroll 200 participants. Led by Ohio State University, it is expected to complete by March 1, 2029. The latest data from ClinicalTrials.gov was last updated on February 23, 2026.
Brief Summary
Food and Fitness with Medicine (FFWM) is a 24-week randomized controlled trial (RCT) enrolling 200 post-menopausal women (PMW) with stage 2 cardio-kidney metabolic (CKM) syndrome and type-2 diabetes (T2D) within 6 weeks of initiating glucagon-like peptide-1 receptor agonist (GLP-1RAs) to: 1. Examine discontinuation rates of GLP-1RAs (primary outcome); 2. Compare change in American Heart Association (AHA) PREVENT scor...Show More
Official Title

Food and Fitness With Medicine

Conditions
Cardiovascular Kidney Metabolic SyndromeType 2 Diabetes
Other Study IDs
  • FFWM
  • STUDY20250193
NCT ID Number
Start Date (Actual)
2026-01-14
Last Update Posted
2026-02-23
Completion Date (Estimated)
2029-03
Enrollment (Estimated)
200
Study Type
Interventional
PHASE
N/A
Status
Recruiting
Keywords
Food is Medicine
Cardiovascular-kidney-metabolic
Exercise is Medicine
Post-menopausal Women
Medically Tailored Groceries
Type 2 Diabetes
Glucagon-like Peptide 1 Receptor Agonists
Nutrition
Behavior
GLP-1
Weight
Fitness
Primary Purpose
Supportive Care
Design Allocation
Randomized
Interventional Model
Parallel
Masking
None (Open Label)
Arms / Interventions
Participant Group/ArmIntervention/Treatment
ExperimentalFFWM+
Intervention Group receives medically tailored groceries and culinary training, fitness education and training, behavioral reinforcers, and access to a secure web portal.
Exercise is Medicine (EIM)
During Phase 1 (Weeks 1-12), participants are enrolled in a comprehensive 12-week fitness education and training program.
Culinary Education
During Phase 1 \& 2, participants receive monthly hybrid cooking demonstrations with culinary training.
Food is Medicine
During Phase 1 (Weeks 1-12), participants receive bi-weekly medically tailored grocery vouchers.
Nutrition Counseling
During Phase 1 (Weeks 1-12), participants engage in weekly behavioral nutrition counseling.
Participant Website
During Phases 1 and 2, participants will receive digital behavioral reinforcers and access to a secure web portal that provides evidence-based resources.
No InterventionStandard Care
Control Group - access to optional cooking demos
N/A
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
GLP-1 RA discontinuation rates
GLP-1RA discontinuation rates will be captured using the electronic medical record to obtain medication name and formulation, dosage and frequency, prescription start and end dates, prescribing provider, refill information and prescription status (active, discontinued, completed), clinic notes or medication reconciliation fields confirming ongoing use or discontinuation, pharmacy records indicating medication pick-up (when available).
0, 12, and 24 weeks
Secondary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
American Heart Association (AHA) PREVENT Scores
The AHA PREVENT scores are used in cardiovascular research to estimate the risk of future cardiovascular disease (CVD) based on factors such as BMI, age, sex, cholesterol, blood pressure, smoking, eGFR, diabetes, medication use, UACR, zip, and HbA1c. Scores are reported as a percent risk for CVD using the following scale: low (\<5%), borderline (5% to 7.4%), intermediate (7.5% to 19.9%), and high (\>20%).
0, 12, and 24 weeks
Metabolites
Stool and urine samples will be collected from participants to analyze metabolites at 3 study time points. Participants will collect samples and return within 7 days of a clinic visit. Samples will be processed and stored under strict biosafety protocols to maintain integrity.
0, 12, and 24 weeks
Life's Essential 8 Scores
The Life's Essential 8 Survey is a combination of questions used to assess and needed to accurately collect data to determine Life's essential 8 (LE8 scores for participants). Questions collect data on lifestyle health behaviors such as sleep patterns and smoking status. The Life's Essential 8 (LE8) is scored on a scale of 0 to 100. The LE8 score is used to assess and track an individual's overall cardiovascular health based on 8 key factors with a higher score indicating better cardiovascular health.
0, 12, and 24 weeks
Blood Lipids
Trained phlebotomists will perform a venous blood draw. The total amount of blood that will be collected for lipids (total cholesterol, high density lipoprotein (HDL), low density lipoprotein (LDL)) for this entire research study (3 time points over 24 weeks) is less than 2.5 mL (\<1 teaspoon).
0, 12, and 24 weeks
Body Composition
We will look at body composition to monitor shifts in muscle mass, body fat, and visceral fat throughout the intervention. Participants will be weighed, wearing light clothing and without shoes, on a calibrated bioelectrical impedance scale (seca mBCA Ultra) capable of analyzing body composition including visceral fat, total body fat percentage, lean body mass, and resting energy expenditure.
0, 12, and 24 weeks
Dietary Patterns
The National Cancer Institute's Dietary History Questionnaire (DHQIII) will be used to assess dietary patterns. The DHQIII tool is validated and assesses dietary intake of 134 foods and beverages in the past 30 days using the Healthy Eating Index score. Scores range 0-100 with higher scores indicating better overall diet quality.
0, 12, and 24 weeks
Hip Circumference
Hip circumference will be measured with a measuring tape following the current NHANES Anthropometry Procedures Manual.
0, 12, and 24 weeks
Dermal Carotenoid Scores
Resonance Raman spectroscopy (RRS) is a non-invasive, validated method of measuring dermal carotenoids as a biomarker of fruit and vegetable intake. The Pharmanex NuSkin Biophotonic Scanner (model S3) uses a standardized RSS protocol intended for nutritional purposes and will not be used to diagnose any disease or medical condition. The scan involves passing a safe LED light across the surface of the skin for approximately 2 minutes. 2-3 measures will be obtained at each time point.
0, 12, and 24 weeks
Blood Pressure
Blood pressure including both systolic and diastolic blood pressure measures will be checked via an automated oscillometric sphygmomanometer (Omron 7 series).
0, 12, and 24 weeks
Nutrition Security
The Center for Nutrition and Health Impact Nutrition Security Screener will be used to assess nutrition security. The Center for Nutrition and Health Impact developed a four-item nutrition security screening tool. Three questions ask about household consumption and concerns around foods thought by the respondent to be good (or not) for health and well-being, and a fourth question asks about food variety.
0, 12, 24 weeks.
Social and Emotional Wellbeing
The De Jon Gierveld Social Isolation Scale will be used to asses social and emotional wellbeing. This short form, 6-item scale can be used as a reliable and valid measurement instrument for overall, emotional, and social loneliness. For this scale each item is assigned a score of 0 or 1 with the total possible score ranging form 0 to 6 with high scores indicating higher rates of loneliness.
0, 12, and 24 weeks
Social Needs
Centers for Medicare and Medicaid Services Accountable Health Communities Health-Related Social Needs Screening Tool will be used to identify needs. Tested by the CMS Innovation, this tool addresses the critical gap between clinical care and community services in the current health care delivery system by testing whether systematically identifying and addressing the health-related social needs of Medicare and Medicaid beneficiaries impacts their total health care costs and improves health. The questionnaire includes 26 questions addressing living situation, food security, transportation, utilities, safety, financial strain, employment, family and community support, education, physical activity, substance abuse, mental health and disabilities. This screening tool is not scored on a standardized scale rather participants screening positive for unmet social needs will be referred to available and free community resources (e.g., Health Impact Ohio, SNAP, MidOhio Food Farmacy, etc).
0, 12, and 24 weeks
HbA1c
Trained phlebotomists will perform a venous blood draw. The total amount of blood that will be collected for HbA1c for this entire research study (3 time points over 24 weeks) is less than 2.5 mL (\<1 teaspoon).
0, 12, and 24 weeks
Waist Circumference
Waist circumference will be measured with a measuring tape following the current NHANES Anthropometry Procedures Manual.
0, 12, and 24 weeks
Food Noise
The Food Noise Questionnaire (FNQ) is a 5-item instrument to assess the frequency and intensity of intrusive food-related thoughts, urges, and preoccupations. Each item is scored 0-5, with a total score range of 0-20. Higher scores indicate greater perceived food noise.
0, 12, 24 and weeks
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
Female
  • Diagnosis of at least one of the following conditions: hypertension, type 2 diabetes, hyperlipidemia, chronic kidney disease, and/or metabolic syndrome.
  • At least 18 years of age at the time of signing consent.
  • Participants must have reliable transportation to attend Exercise is Medicine sessions.
  • Access to an internet-enabled device.
  • No objections to online grocery shopping, home food deliveries, or nutrition counseling.
  • Residence meets Instacart delivery requirements (e.g., non-institutionalized).
  • Participant is willing to use a personal credit card for Instacart back-up payments.
  • Participants must speak English to be able to consent and engage in FIM and EIM programs.
  • Participant has been clinically prescribed GLP-1RA's.

  • Conditions that impact digestion, metabolism, or food intake (e.g. surgical loss of esophagus, stomach, or colon, pancreatic dysfunction, bariatric surgery, brain surgery that alters cognition, etc.).
  • Participants with uncontrolled mental illness disorders (e.g., schizophrenia, bipolar disorder, major depression, etc.) that are not well-managed or controlled through treatment, as determined by the study team.
  • Familial history of certain cancers (e.g., multiple endocrine neoplasia, medullary thyroid carcinoma, etc.).
  • Active digestive illnesses (i.e., Celiac disease, irritable bowel syndrome, chronic malabsorption).
  • Comorbidities such as psychiatric or general illness that may put the subject at risk as determined by the investigator/s.
  • Renal impairment, eGFR < 60 ml/min/1.73m2
  • Factor which, in the investigator's opinion, is likely to compromise the subject's ability to participate in the study.
  • Recent participation (e.g., 3 months) in other behavioral nutrition trials or programs (i.e., bariatric programs, diabetes education programs).
  • Currently pregnant or planning to become pregnant during the study.
  • Participant is not willing to provide a urine, blood, or stool sample.
Ohio State University logoOhio State University456 active studies to explore
American Heart Association logoAmerican Heart Association
Study Responsible Party
Colleen Spees, PhD, RD, FAND, FAHA, Principal Investigator, Professor of Medical Dietetics and Director of Hope Lab, Ohio State University
Study Central Contact
Contact: Jenna N Hauben, BS, 9083344689, [email protected]
Contact: Cara L Chase, BS, 5032789721, [email protected]
4 Study Locations in 1 Countries

Ohio

Ohio State Healthy Community Center, Columbus, Ohio, 43062, United States
Active, not recruiting
Ohio State East Hospital, Columbus, Ohio, 43203, United States
Luiza Reopell, MBA, Contact, 614-572-9191, [email protected]
Not yet recruiting
Martha Morehouse, Columbus, Ohio, 43221, United States
Jenna Hauben, Contact, 908-334-4689, [email protected]
Recruiting
Ohio State Outpatient Care Upper Arlington, Upper Arlington, Ohio, 43221, United States
Active, not recruiting