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NCT07376226Not yet recruiting

Effects of Whole Fruit on Blood Sugar in People With Type 2 Diabetes

Effects of Whole Fruit on Glycemic Control, Liver Fat, and Cardiovascular Disease Risk Factors in Adults With Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 7 Jul 2026

Brief summary (registry, in English)

This study will determine the effects of consuming whole fruit on blood sugar control, liver fat, and cardiovascular health in adults with type 2 diabetes who are not treated with insulin.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
25 (estimated)
First submitted
22 Jan 2026
Start date
Sept 2026
Primary completion date
Oct 2027
Lead sponsor
Harvard School of Public Health (HSPH)
NCT number
NCT07376226

What you commit to

  • Study type: Interventional
  • Planned participants: 25
  • From Sept 2026 to the primary completion date, Oct 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

  • On weight loss medication, including GLP-1 receptor agonists (e.g., semaglutide, dulaglutide)
  • Change in the dosage of a chronic medication that may affect study endpoints within the past 3 months

Other illness

  • Evidence of latent autoimmune diabetes (LADA) or maturity-onset diabetes of the young (MODY)
  • Heart attack in the past 6 months or severe/unstable heart failure
  • Significant gastrointestinal disease, major gastrointestinal surgery, or gallstones
  • Significant cardiovascular, renal, cardiac, liver, lung, adrenal, or nervous system disease that might compromise participant safety or data validity
  • Evidence of cancer (other than non-melanoma skin cancer) within the last 5 years
  • Major psychiatric condition that would affect the ability to participate in the study
  • Not able to eat the provided study meals (e.g., food allergies)

Lab values

  • Estimated glomerular filtration rate (eGFR) \<45 ml/min per 1.73 m²
  • Clinically significant laboratory abnormality (e.g., abnormal hemoglobin levels)

Other

  • On insulin
  • Lost or gained more than 5 lbs (or more than 2% of body weight if the patient weighs \>250 lbs) of weight in the past 2 months
  • Pregnant, planning to become pregnant in the next 6 months, or breastfeeding
  • Behavioral factors or circumstances that may impede adherence to the dietary intervention
  • Not able to undergo the MRI scan (e.g., due to claustrophobia, implanted metal objects, or body girth ≥60 cm)

Who the study is looking for

  • Aged ≥18 years
  • Diagnosed with type 2 diabetes
  • HbA1c between 6.5-12.0%
  • Fasting C-peptide level ≥0.5 ng/ml, indicating the patient does not have beta-cell failure, as measured at screening

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Harvard T.H. Chan School of Public Health
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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