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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05888454
Other study ID # Dando pasos juntos
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 24, 2023
Est. completion date July 2024

Study information

Verified date February 2024
Source Hospital San Jose Tec de Monterrey
Contact Regina Moreno, MD
Phone +52 33 367 668 77
Email regina.moreno@tecsalud.mx
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Integrative Group Program
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.
Conventional treatment for T2DM
Conventional medical treatment for T2DM

Locations

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

Sponsors (3)

Lead Sponsor Collaborator
Hospital San Jose Tec de Monterrey Fundación Santos y de la Garza Evia I.B.P, TecSalud

Country where clinical trial is conducted

Mexico, 

Outcome

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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