Lifestyle Intervention for Type 2 Diabetes in Primary Care (CREDOenAP)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorParc Sanitari Pere Virgili

About this trial

The purpose of this clinical trial is to determine whether an intensive lifestyle intervention can achieve remission of type 2 diabetes mellitus (T2DM) in adult patients treated in primary care. The main questions the study seeks to answer are:

* What proportion of participants achieve diabetes remission after 6 months of intervention? * How many participants maintain remission 12 months after completing the program (18 months total)?

Participants will:

* Follow a personalized dietary plan with carbohydrate restriction. * Engage in moderate, accessible physical activity. * Implement strategies to improve circadian rhythm regularity. * Receive psychological counseling and support.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Signed informed consent.

Men and women aged 18-80 years, inclusive.

Confirmed diagnosis of T2DM according to recognized diagnostic criteria

Most recent recorded hemoglobin A1c (HbA1c) > 6.5%.

Disqualifiers

Failure to meet the diagnostic criteria for T2DM in the screening laboratory tests.

Being dependent for basic activities of daily living (Barthel score ≤ 90 points).

Lack of willingness to cooperate with the follow-up of the lifestyle intervention plan.

Presence of serious or terminal comorbidities significantly worsening short- to medium-term prognosis (active cancer, terminal chronic diseases, myocardial infarction within the last 6 months, acute heart failure or NYHA stage ≥ III, etc.).

Trial design

Design model

Parallel

Treatments tested in this trial

  • CREDOenAP intervention

    Behavioral

    Intervention program with intensive lifestyle counseling, added to standard pharmacological treatment subsequently adjusted according to clinical needs and outcomes. The intervention will last 6 months and consists of biweekly in-person and telephone visits. Patients will follow a personalized dietary plan with carbohydrate restriction, based on the recommendations of the American Diabetes Association; engage in moderate and accessible physical activity; implement circadian rhythm regularization; and receive psychological counseling and support.

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Presence of T2DM remission

Glycated hemoglobin (HbA1c): T2DM remission will be considered if HbA1c is \< 6.5% after 6 months of intervention and at least 3 months without antidiabetic medication. HbA1c will be determined by blood analysis after a minimum of 8 hours of fasting Fasting plasma glucose: T2DM remission will be considered if fasting venous plasma glucose is \< 126 mg/dL after 6 months of intervention and at least 3 months without antidiabetic medication. Fasting plasma glucose will be measured by venous blood analysis after a minimum of 8 hours of fasting

Time frame
After 6 months of intervention and 12 months after the intervention

Secondary outcomes

1

Blood pressure

Blood pressure will be measured three times after the participant has been seated at rest for 10 minutes with uncrossed legs. The mean of the last two measurements will be used for statistical analysis. Systolic and diastolic blood pressure will be reported in mmHg using a brachial cuff sphygmomanometer.

Time frame
After 6 months of intervention and 12 months after the intervention.
2

Total cholesterol

Measured in mg/dL via blood analysis.

Time frame
After 6 months of intervention and 12 months after the intervention
3

HDL cholesterol

High-density lipoprotein (HDL) cholesterol measured in mg/dL via blood analysis.

Time frame
After 6 months of intervention and 12 months after the intervention
4

LDL cholesterol

Low-density lipoprotein (LDL) cholesterol measured in mg/dL via blood analysis.

Time frame
After 6 months of intervention and 12 months after the intervention

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: