Status:
RECRUITING
Whole Food for Families: A Pilot RCT of a Dietary Guidelines-Based Intervention to Prevent Type 2 Diabetes
Lead Sponsor:
Vanderbilt University
Collaborating Sponsors:
Vanderbilt University Medical Center
Conditions:
PreDiabetes
Diet, Healthy
Eligibility:
All Genders
6-59 years
Phase:
NA
Brief Summary
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-child pairs after a 12-week famil...
Detailed Description
This dietary program is based on empirical evidence showing that a diet pattern that favors minimally processed and whole foods (e.g., whole grains, fruits, vegetables, nuts) in contrast to diet patte...
Eligibility Criteria
Inclusion
- For this study, eligible adults will be those that:
- are 25 to 59 years of age at time of initial screen and identify as a parent to at least one child or adolescent 6-18 years;
- have a body mass index of between ≥23kg/m2 to \<40kg/m2;
- 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);
- have no special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages;
- are English speaking;
- reside in Greater Nashville Tennessee and willing to come to Vanderbilt campus and Vanderbilt University Medical Center for required study visits;
- are without medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis);
- 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:
- Are 6-18 years at time of initial screen;
- Have an index parent with prediabetes that is actively enrolled in the program;
- have body mass index ≥5th percentile for age and gender on standardized CDC growth curves;
- have no special dietary restrictions or food allergies that would prohibit consumption of a variety of foods/beverages;
- have parental commitment to participate in a 12-week research study
- are English speaking;
- reside in the Greater Nashville Tennessee area and live at home with their index parent during the duration of 12- week study;
- are without medical conditions that would limit participation in a diet-related study (e.g., tube feeding, dysphagia, severe food allergy causing anaphylaxis);
- are able to participate in a 12-week dietary program that includes at least dinner and snacks provided during after-school hours;
Exclusion
- Adult exclusion criteria include:
- Adults who's HbA1c test is outside of the HbA1c range during screening\* (see details related to screening results)
- adults outside the specified age range of \<25 years or \>59 years;
- adults whose body mass index is \<23kg/m2 or those with a body mass index ≥40kg/m2 as that degree of morbid obesity represents a different phenotype where dietary behavioral intervention alone may not be sufficient to achieve weight loss);
- 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;
- adults actively participating in any type of weight loss program (dietary or physical activity)
- adults with a prior history of type 2 diabetes;
- adults who are not English speaking or have limited English-language proficiency;
- adults with special dietary restrictions, food allergies, or medical conditions that prohibit participation in a diet-related study;
- adults with serious mental or neurologic illness that impairs the ability to consent/participate;
- women who are pregnant or nursing due to increased metabolic state requiring greater energy requirements;
- adults currently taking medications to treat diabetes or to promote weight loss;
- adults living outside Greater Nashville Tennessee or who are unwilling to travel to Vanderbilt for study visits;
- adults who do not otherwise meet the eligibility criteria listed in sections above as determined by pre-screen;
- Offspring (child\[ren\] and adolescent\[s\]) exclusion criteria include:
- children/adolescents outside the specified age range of \<6 years or \>18 years;
- children/adolescents whose body mass index is \<5th percentile for age and gender on standardized CDC growth curves;
- children/adolescents who do not have an eligible index parent participating in the study;
- children who do not have parental commitment to participate consistently for 12-weeks
- children/adolescents who are not English speaking or have limited English-language proficiency;
- children/adolescents with special dietary restrictions, food allergies, or medical conditions that prohibit participation in a diet-related study;
- children/adolescents who display dissenting behaviors during baseline data collection;
- children/adolescents actively participating in any type of weight loss program (medical or lifestyle);
- children/adolescents who do not otherwise meet the eligibility criteria listed in sections above as determined by pre-screen;
Key Trial Info
Start Date :
October 13 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2027
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT06482944
Start Date
October 13 2025
End Date
June 30 2027
Last Update
October 21 2025
Active Locations (1)
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1
Vanderbilt University School of Nursing
Nashville, Tennessee, United States, 37240