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Testing an Education Program for Blood Sugar Control in Type 2 Diabetes

Tests the Ask Me 3® education program in adults with type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Glycemic Control and the Ask Me 3® Educational Program

Key facts

Where
San Nicolás de los Garza, MexicoSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07678671, who can take part

Where in Mexico

  • Hospital Clinica Nova de MonterreySan Nicolás de los Garza, MexicoNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Maria Elena Romero Ibarguengoitia
Trial code
NCT07678671
Record updated
17 September 2026
Original description
The goal of this clinical trial is to determine whether the Ask Me 3® educational program improves glycemic control in adults with type 2 diabetes mellitus receiving care at a metabolic clinic. The main questions it aims to answer are:Read full original descriptionShow less

Difference in Glycemic Control Among Patients With Type 2 Diabetes Mellitus Receiving the Ask Me 3® Educational Program: A 3-Month Follow-Up Study

The goal of this clinical trial is to determine whether the Ask Me 3® educational program improves glycemic control in adults with type 2 diabetes mellitus receiving care at a metabolic clinic. The main questions it aims to answer are:

Does participation in the Ask Me 3® educational program improve glycated hemoglobin (HbA1c) and fasting plasma glucose levels after a 3-month follow-up?

Researchers will compare participants who receive the Ask Me 3® educational program with those who receive standard medical care alone to determine whether the educational intervention improves glycemic control.

Participants will:

Provide written informed consent and undergo eligibility assessment. Be randomly assigned to either the intervention group or the control group. Complete baseline assessments, including demographic information, anthropometric measurements, medical history, dietary habits, physical activity, diabetes education, and nutritional counseling history.

Have baseline HbA1c and fasting plasma glucose values collected from their medical records.

Receive either the Ask Me 3® educational program (intervention group) or standard care (control group).

Attend routine follow-up visits over a 3-month period. Complete a final evaluation, including repeat clinical measurements and collection of HbA1c and fasting plasma glucose values to assess changes in glycemic control.

Inclusion: Adults aged 18 years or older; Beneficiaries of Hospital Clínica Nova; Male and female participants; Confirmed diagnosis of type 2 diabetes mellitus according to the institution's established clinical practice guidelines; Patients receiving care at the Metabolic Clinic.

Exclusion: Patients receiving palliative care; Patients with autoimmune, immunological, or oncological comorbidities; Patients with cognitive or psychiatric conditions that impair their ability to provide informed consent independently (e.g., delirium, schizophrenia, or similar conditions); Pregnant women.

ClinicalTrials.gov NCT07678671