Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Dando Pasos Juntos: An Integrative Group Program for Type 2 Diabetes Mellitus
This is an open, randomized, controlled trial to determine the impact of an integrative group program on metabolic control and wellbeing perception of patients with T2DM. The integrative group program consists of 6 in-person sessions directed by a health coach and occurring every other week, and 6 asynchronous educative sessions during a period of 12 weeks.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | July 2024 |
Est. primary completion date | July 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - T2DM diagnosis of less than 5 years - Age 18 to 80 years - Current residence in Nuevo León, México - Availability to attend in-person sessions - Provides written informed consent - Able to read and write Exclusion Criteria: - Currently under insulin treatment - T2DM diagnosis more than 5 years ago - Comorbidities such as active cancer, acquired immunodeficiency (HIV+, AIDS), liver, cardiovascular, renal, pulmonary or thyroid disease. - History of severe neurologic or psychiatric disease (current or past diagnosis) - Currently pregnant or intention of pregnancy in the following 3 months - Males that consume more than 4 alcoholic beverages daily or 14 weekly - Females that consume more than 3 alcoholic beverages daily or 7 weekly - Consumption of any illicit drug |
Country | Name | City | State |
---|---|---|---|
Mexico | Centro Médico Zambrano Hellion, Fundación Santos y de la Garza Evia I.B.P, TecSalud | San Pedro Garza Garcia | Nuevo León |
Mexico | Centro de Salud Integral, Fundación Santos y de la Garza Evia I.B.P, TecSalud | Santa Catarina | Nuevo León |
Lead Sponsor | Collaborator |
---|---|
Hospital San Jose Tec de Monterrey | Fundación Santos y de la Garza Evia I.B.P, TecSalud |
Mexico,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | HbA1c levels (%) | Baseline to 12 weeks | ||
Secondary | HbA1c levels (%) | Baseline to 12 weeks and 36 weeks | ||
Secondary | Fasting insulin (mU/mL) | Baseline to 12 weeks and 36 weeks | ||
Secondary | Fasting glucose (mg/dL) | Baseline to 12 weeks and 36 weeks | ||
Secondary | Homeostatic Model Assessment (HOMA index) | Baseline to 12 weeks and 36 weeks | ||
Secondary | High-sensitivity C-reactive protein (hs-CRP, mg/dL) | Baseline to 12 weeks and 36 weeks | ||
Secondary | Change in lifestyle instrument | Instrument to measure diabetic lifestyles (IMEVID) total score | Baseline to 12 weeks and 36 weeks | |
Secondary | Subjective sense of wellbeing instrument | Positive emotion, Engagement, Relationships, Meaning, and Accomplishment (PERMA-profiler) score | Baseline to 12 weeks and 36 weeks | |
Secondary | Adherence to pharmacological interventions for T2DM | Adherence to Refill and Medication Scale (ARMS) score | Baseline to 12 weeks and 36 weeks | |
Secondary | Change in dose of pharmacological interventions for T2DM | Baseline to 12 weeks and 36 weeks |
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