Home › Prediabetes › NCT06482944
Whole Food for Families: A Pilot RCT of a Dietary Guidelines-Based Intervention to Prevent Type 2 Diabetes
Who can join
Ages 6 to 59 · All sexes
Full eligibility criteria
For this study, eligible adults with prediabetes will be those that: 1. are 25 to 59 years of age at time of initial screen and identify as a parent to at least one offspring 6-26 years or identify as a spouse/partner to an adult 25-64 years; 2. have a body mass index of between ≥23kg/m2 to ≤45kg/m2; 3. have prediabetes (based on American Diabetes Association criteria of either fasting plasma glucose of ≥100 mg/dL, HgbA1c 5.7-6.4%, or 2-hour plasma glucose during 75-g oral glucose tolerance test \[OGTT\] 140 mg/dL to 199 mg/dL) with recent lab values reported within the prior 6-12 months and confirmed by an HbA1c A1cNow+ collected prior to enrollment (\*see comment below); 4. have no special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages; 5. are English speaking; 6. reside in Greater Nashville Tennessee and willing to come to Vanderbilt campus and Vanderbilt University Medical Center for required study visits; 7. are without medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis; history of or active eating disorder); 8. are able to participate in a 12-week dietary program that requires home preparation/cooking for meals and snacks; For this study, eligible offspring will be those that: 1. Are 6-26 years at time of initial screen; 2. Have an index parent with prediabetes that is actively enrolled in the program; 3. have body mass index ≥5th percentile for age and gender on standardized CDC growth curves; 4. have no special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages; 5. have parental commitment to participate in a 12-week research study 6. are English speaking; 7. reside in the Greater Nashville Tennessee area and live at home with their index parent during the duration of 12- week study; 8. are without medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis, history or active eating disorder); 9. are able to participate in a 12-week dietary program that includes at least dinner and snacks provided during after-school hours; For this study, eligible spouse/partner will be those that: 1. Are 25-64 years at time of initial screen; 2. Be considered a spouse/partner of an adult with prediabetes that is actively enrolled in the program; 3. have no special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages; 4. are English speaking; 5. reside in the Greater Nashville Tennessee area and live in the home of the enrolled adult with prediabetes during the duration of 12- week study; 6. are without medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis, history or active eating disorder); Adult with prediabetes exclusion criteria include: 1. Adults whose HbA1c test is outside of the HbA1c range during screening\* (see details related to screening results) 2. adults outside the specified age range of \<25 years or \>64 years; 3. adults whose body mass index is \<23kg/m2 or those with a body mass index ≥46kg/m2 as that degree of morbid obesity represents a different phenotype where dietary behavioral intervention alone may not be sufficient to achieve weight loss); 4. receiving care by a healthcare provider (i.e., MD, NP, PA) for a complicated diagnosis of prediabetes that requires routine glycemic monitoring or frequent healthcare visits for management/treatment; 5. adults actively participating in any type of weight loss program (dietary or physical activity) 6. adults with a prior history of type 2 diabetes; 7. adults who are not English speaking or have limited English-language proficiency; 8. adults with special dietary restrictions, food allergies, or medical conditions that prohibit participation in a diet-related study; 9. adults with serious mental or neurologic illness that impairs the ability to consent/participate; 10. women who are pregnant or nursing due to increased metabolic state requiring greater energy requirements; 11. adults currently taking medications to treat diabetes or to promote weight loss; 12. adults living outside Greater Nashville Tennessee or who are unwilling to travel to Vanderbilt for study visits; 13. adults who do not otherwise meet the eligibility criteria listed in sections above as determined by pre-screen; Offspring exclusion criteria include: 1. offspring outside the specified age range of \<6 years or \>26 years; 2. offspring (under 18 years) whose body mass index is \<5th percentile for age and gender on standardized CDC growth curves; 3. offspring who do not have an eligible index parent participating in the study; 4. children (under 18 years) who do not have parental commitment to participate consistently for 12-weeks 5. offspring who are not English speaking or have limited English-language proficiency; 6. offspring with special dietary restrictions, food allergies, or medical conditions that prohibit participation in a diet-related study; 7. offspring with active or history of eating disorder; 8. children/adolescents (under 18 years) who display dissenting behaviors during baseline data collection; 9. offspring who do not otherwise meet the eligibility criteria listed in sections above as determined by pre-screen; Spouse/partner exclusion criteria include: 1. Spouse/partner outside the specified age range \<25 year or ≥65 years; 2. Does not identify as a spouse/partner of the adult with prediabetes that plans to be enrolled in the program; 3. Spouse/partner with special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages; 4. Spouse/partner who are not English speaking or have limited English-language proficiency; 5. Spouse/partner who does not reside in the Greater Nashville Tennessee area and/or does not live in the home of the enrolled adult with prediabetes during the duration of 12- week study; 6. Spouse/partner with medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis, history or active eating disorder);
About the study
This study will address the following aims:
Aim 1 (primary): Conduct a pilot RCT to evaluate the feasibility, acceptability, enrollment, and retention rates of adult-offspring pairs or adult-spouse/significant other pairs after a 12-week family-centered, non-calorie restricted whole foods diet.
Aim 2: Conduct a pilot RCT to evaluate the preliminary effectiveness of a non-calorie restricted whole foods diet on adult HbA1c at 12-weeks and adult/offspring or adult/spouse or significant other diet quality during the 12-week intervention.
Aim 2a: Evaluate intervention effects on HbA1c measures in adults with prediabetes.
Aim 2b: Evaluate intervention effects on the diet quality (via the 2020 HEI) of adults and offspring.
Aim 3: Conduct family focus groups to understand how SDOH and individual/family needs and preferences may be perceived barriers or facilitators of diet adherence.
What is being tested
- Whole Foods for Families (behavioral)
Sponsor: Vanderbilt University · Participants: 30 · Started: Oct 13, 2025
Contact the study team
- Nadia M. Sneed, PhD, MSN · Phone: 615-343-1542
Official record on ClinicalTrials.gov — NCT06482944
Locations in the U.S.
| Tennessee | Vanderbilt University School of Nursing, Nashville |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.