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NCT07850531Not yet recruiting

Precision Nutrition for Obesity and Prediabetes Prevention in Under-supported Communities

Building Capacity in Precision Nutrition to Address Obesity and Diabetes in Underserved Communities

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

This randomized controlled trial will evaluate the effectiveness of a culturally sensitive precision nutrition intervention for improving obesity- and diabetes-related outcomes among African American and Hispanic/Latino adults who are overweight, obese, or have prediabetes. Participants will be randomized to either a precision nutrition intervention group or a control group receiving standard nutrition counseling and educational materials. The intervention incorporates individualized dietary recommendations based on participant characteristics, including dietary habits, physical activity, socioeconomic factors, psychosocial factors, phenotype, and genotype. Outcomes will be assessed at baseline, 6 weeks, and 12 weeks and will include body weight, diet quality, fasting blood glucose, hemoglobin A1C, body composition, physical activity, blood pressure, and metabolic biomarkers. Feasibility, acceptability, and sustainability of the intervention will also be evaluated.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
14 Sept 2026
Start date
1 Oct 2026
Primary completion date
31 Aug 2027
Lead sponsor
Prairie View A&M University
Diseases
Obesity
NCT number
NCT07850531

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 1 Oct 2026 to the primary completion date, 31 Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Following a prescribed diet for any reason, including weight loss, within the previous 3 months

Other illness

  • Diagnosed diabetes mellitus
  • Cardiovascular disease
  • Eating disorders
  • Lung disease
  • Liver disease
  • Thyroid disease
  • Crohn's disease

Other

  • Do not meet the inclusion criteria
  • Pregnant
  • Lactating

Who the study is looking for

  • Adults aged 18 to 65 years
  • African American or Hispanic/Latino adults
  • Residents of Texas
  • Body mass index (BMI) ≥ 25 kg/m² and/or fasting blood glucose levels of 100-125 mg/dL
  • Hemoglobin A1C (HbA1C) between 5.7% and 6.4%
  • Daily access to a cell phone and the internet
  • Able to participate in moderate-to-vigorous physical activity
  • Able and willing to provide informed consent

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
integrated Nutrition Intervention for Community and Health Enhancement Laboratory (iNICHE Lab)
Coordinator of this site? Confirm its status
Prairie ViewUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.