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NCT07598773Enrolling by invitation

BETA: Study in Prediabetes Type 2 Diabetes

Beta-cell Evaluation Through Data-driven Assessments (BETA): Study in Prediabetes Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

This study is testing the feasibility of using non-invasive, remote digital tools including continuous glucose monitors (CGMs) and the Oura Ring to predict the function of beta-cells, the cells in the pancreas that secrete insulin. This study is being done in individuals with prediabetes or Type 2 diabetes. The aim is to develop remote digital tools that can predict the health and functioning of the pancreas in people with prediabetes or Type 2 diabetes, allowing personalized treatment approaches to preserve insulin secretion.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
130 (estimated)
First submitted
14 May 2026
Start date
25 Mar 2026
Primary completion date
1 Feb 2027
Lead sponsor
4YouandMe
NCT number
NCT07598773

What you commit to

  • Study type: Observational
  • Planned participants: 130
  • From 25 Mar 2026 to the primary completion date, 1 Feb 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

  • Using any of the following medications: Glucocorticoids, Non-Selective Beta Blockers (e.g., propranolol), Thiazide Diuretics
  • Currently using tobacco products (cigarettes, vapes, chew, dip, etc.)

Other illness

  • Dairy or soy allergy
  • Diagnosed with Type 1 diabetes or MODY (Maturity-Onset Diabetes of the Young)
  • History of pancreatic disease (other than diabetes) or pancreatic transplantation
  • Have any active malignancy within the last 12 months

Lab values

  • History of bariatric / other gastrointestinal surgery anticipated to affect glucose metabolism / cause gastroparesis
  • History of systemic disease (hepatic, cardiovascular, other) likely to interfere with glucose metabolism or study participation

Other

  • Using any Abbott CGM (prescribed or OTC)
  • BMI \<18 kg/m2 or \>40 kg/m2
  • Currently pregnant or breastfeeding
  • Using an insulin pump
  • Hospitalized overnight for any reason in the last 3 months

Who the study is looking for

  • 18+ years old
  • Have an established diagnosis of Prediabetes or Type 2 diabetes
  • Have a glycated hemoglobin (HbA1c) below 8% (64 mmol/mol) and a body mass index (BMI) between 18-40 kg/m2 that will be determined from your height and weight
  • Are willing to use an Abbott FreeStyle Libre 3/3+ Continuous Glucose Monitor (CGM) supplied by the study and provide the study investigators access to the CGM data
  • Are willing to use the study wearable devices (e.g., Oura Ring)
  • Are able to read, write, and speak in English
  • If you use long-acting insulin, you must be on a prescribed regimen where you administer it at bedtime only and no other time of day (bolus short-acting may be used at any time as needed)
  • All medication regimens must have a minimum of 30 days supply, and no new medications started within 30 days of enrollment
  • Weight must be stable (± 10 pounds) for 2 months prior to enrollment
  • Must have a personally owned iPhone 6s or newer (iOS 16.4+) or Android smartphone (version 12 or newer) and use this phone to download and use the study app and use the provided study devices
  • Must have a personally owned computer or tablet or have access to these devices at home
  • Must reside in the North San Francisco Bay area and be willing to travel to Novato, CA to attend two morning clinic assessments at the Buck Institute

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Buck Institute for Research on Aging
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

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