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Translational Study for Obesity Management in Mexican Adults Using the Group Lifestyle Balance Program

Translational Study for Overweight and Obesity Management in Adults Using the Group Lifestyle Balance Program in Primary Care Clinics and Public Hospitals From Sonora, México

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02537704
Acronym
GLBOMEX
Enrollment
258
Registered
2015-09-02
Start date
2015-09-30
Completion date
2017-04-30
Last updated
2016-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Overweight

Keywords

Obesity, Translational, Diabetes Prevention Program, Group Lifestyle Balance Program

Brief summary

Obesity is the main modifiable risk factor for the development of chronic diseases in Mexico. Several randomized controlled trials have shown that intensive lifestyle programs are efficacious for the management of obesity. These programs include frequent sessions (14 or more contacts in the first 6 months) focused on diet and physical activity and use a behavior change protocol. In Mexico most primary care clinics and public hospitals apply traditional treatments for obesity management, which have limited effect on weight loss. This study would provide scientific evidence for an effective model for obesity management. Objective. The purpose of this study is to evaluate the effectiveness of the Group Lifestyle Balance Program for overweight and obesity management in adults, in primary care clinics and public hospitals from Sonora. This is a translational clinical study. Healthcare providers from the participating clinics will be trained with the Group Lifestyle Balance Program before its implementation. The primary outcome measurement is the change in body weight from baseline to 6 months and 12 months. Changes in body mass index, waist circumference, systolic and diastolic blood pressure, depression, quality of life and stress scales will be measured in patients receiving the program before and 6 and 12 months after starting the program. Additionally, biochemical parameters (fasting glucose, total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides, fasting insulin, Homeostatic Model Assessment- Insulin Resistance (HOMA-IR) and liver enzymes \[Aspartate transaminase (AST), Alanine Aminotransferase (ALT)\] will be evaluated from baseline to 12 months.

Interventions

BEHAVIORALGroup Lifestyle Balance Program

Sponsors

Universidad de Sonora
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults (\>18 years of age and \<65) * Overweight or Obese (BMI \>25 kg/m2 y \<50 kg/m2) * Availability and motivation to attend the intervention program * Patients who would benefit from participating in the program according to the health providers * Signing an informed consent

Exclusion criteria

* Medical conditions affecting body weight significantly * Pregnancy or nursing * Bariatric surgery * Being unable to participate in regular moderate physical activity * Blood pressure \>160 mm/Hg * HbA1c\>9

Design outcomes

Primary

MeasureTime frame
Change in body weightChange in body weight from baseline to 6 months and change in body weight from baseline to 12 months

Secondary

MeasureTime frame
Change in the Short Form-36 Health Survey scoreChange in the Short Form-36 Health Survey score from baseline to 6 months and change in the SF-36 Health Survey score from baseline to 12 months
Change in waist circumferenceChange in waist circumference from baseline to 6 months and change in waist circumference from baseline to 12 months
Change in body fat percentageChange in body fat percentage from baseline to 6 months and change in body fat percentage from baseline to 12 months
Change in the Perceived Stress Scale (PSS) -14 scoreChange in the Perceived Stress Scale (PSS) -14 score from baseline to 6 months and change in the Perceived Stress Scale PSS-14 score from baseline to 12 months
Change in systolic and diastolic blood pressureChange in systolic and diastolic blood pressure from baseline to 6 months and change in systolic and diastolic blood pressure from baseline to 12 months
Change in fasting glucoseChange in fasting glucose from baseline to 12 months
Change in the Beck Depression Inventory scoreChange in the Beck Depression Inventory score from baseline to 6 months and change in in the Beck Depression Inventory score from baseline to 12 months
Change in LDL-cholesterolChange in LDL-cholesterol from baseline to 12 months
Change in HDL-cholesterolChange in HDL-cholesterol from baseline to 12 months
Change in triglyceridesChange in triglycerides from baseline to 12 months
Change in fasting insulinChange in fasting insulin from baseline to 12 months
Change in HOMA-IRChange in HOMA-IR from baseline to 12 months
Change in liver enzymes [AST and ALT]Change in liver enzymes [AST and ALT] from baseline to 12 months
Change in total cholesterolChange in total colesterol from baseline to 12 months

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026