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Completed

NCT Number: NCT01831921

Latinos Combating Diabetes

The investigators plan to test two different strategies for weight loss and diabetes prevention in the Latino community in and around Forsyth County, North Carolina. The study is designed to test the hypothesis that a lifestyle weight-loss program implemented within the Latino community will have a more beneficial and clinically meaningful impact on hemoglobin A1c (HbA1c), insulin metabolism, and markers of the metabolic syndrome when compared to an enhanced usual care condition. This lifestyle intervention will include group-based sessions promoting healthy eating, increased physical activity and weight loss. These sessions will be delivered by lay community members, known as Latino Health Advisors (LHAs). The enhanced usual care group will consist of individual counseling with are registered dietitian and uses existing community resources to assist participants in making healthier lifestyle choices.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Wake Forest School of Medicine

Winston-Salem, North Carolina, 27157, United States

About this study

Type 2 diabetes mellitus is a major health concern in the United States, accounting for 90 to 95% of the more than 25 million diagnosed cases of diabetes in 2010. Racial and ethnic minorities are disproportionately affected by the diabetes epidemic, specifically African Americans, Latinos, and Native Americans. Although the cumulative evidence suggests that lifestyle interventions to prevent diabetes can be implemented across a variety of settings with diverse personnel, numerous barriers to widespread dissemination in minority populations still exist. Latinos Combatiendo la Diabetes (La Comunidad) is a 225-participant randomized trial designed to test the hypothesis that a community-based lifestyle weight-loss intervention implemented within the accountability and structure of existing Latino communities will have a more beneficial and clinically meaningful impact on HbA1c, insulin metabolism, and markers of the metabolic syndrome when compared to an enhanced usual care condition. An economic evaluation will also be conducted to determine costs and cost-effectiveness. One trial arm will consist of a group-based intensive lifestyle intervention promoting healthy eating, increased physical activity and modest, yet achievable (5-7%) weight loss delivered in an early 6-month intensive phase followed by an 18-month maintenance phase. Latino Health Advisors (LHAs) will be utilized in the intensive intervention arm. The control arm will consist of an individual educational intervention that incorporates existing community resources that are available to assist residents in making healthier lifestyle choices.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women 18 years and older who reside in or near Forsyth County, North Carolina
  • Self-identified as Hispanic or Latino
  • Evidence of pre-diabetes: Hemoglobin A1c of 5.7-6.5%
  • Body Mass Index (BMI): 25-45 kg/m2
  • Potential participants must be willing to accept randomization to either the intensive lifestyle intervention or the comparison usual care condition

Exclusion criteria

  • Currently involved in a supervised program for weight loss
  • Clinical history of diabetes or newly diagnosed diabetes at screening
  • Clinical history of cardiovascular disease (CVD) occurring within the past 6 months, including myocardial infarction, angina, coronary revascularization, stroke, transient ischemic attack (TIA), carotid revascularization, peripheral arterial disease, congestive heart failure. All persons with recent CVD should be participating in cardiac rehabilitation (with appropriate supervision as indicated) to reduce their risk of recurrence; hence, randomization might raise ethical concerns.
  • Uncontrolled high blood pressure (BP): BP > 160/100. Potential participants can be re-screened after control has been achieved.
  • Pregnancy, breast feeding, or planning pregnancy within 2 years
  • Other chronic disease likely to limit lifespan to less than 2-3 years, including any cancer requiring treatment in past 5 years except non-melanoma skin cancer
  • Chronic use of medicine known to significantly affect glucose metabolism (e.g., corticosteroids, protease inhibitors)
  • Conditions/criteria likely to interfere with participation and acceptance of randomized assignment, including the following: inability/unwillingness to give informed consent, another household member already randomized to La Comunidad, major psychiatric or cognitive problems (schizophrenia, dementia, self-reported active illegal substance or alcohol abuse), participation in another research study that would interfere with La Comunidad.

Treatment and study plan

Lifestyle Weight Loss

Behavioral

Changing diet, physical activity, and self-regulatory behaviors to promote weight loss.

Counseling

Behavioral

Individual nutrition counseling will be delivered by a registered dietitian.

Primary outcomes

  1. Hemoglobin A1c

    Time frame: 6, 12, 18, and 24 months

    Mean hemoglobin A1c in both treatment groups at 6, 12, 18, and 24 months will be assessed.

Secondary outcomes

  1. Body Weight

    Time frame: 6, 12, 18, and 24 months

    Mean body weight in both treatment groups at 6, 12, 18, and 24 months will be assessed.

  2. Systolic Blood Pressure

    Time frame: 6, 12, 18, and 24 months

    Mean systolic blood pressure in both treatment groups at 6, 12, 18, and 24 months will be assessed.

  3. Diastolic Blood Pressure

    Time frame: 6, 12, 18, and 24 months

    Mean diastolic blood pressure in both treatment groups at 6, 12, 18, and 24 months will be assessed.

  4. Fasting Glucose

    Time frame: 6, 12, 18, and 24 months

    Mean fasting plasma glucose in both treatment groups at 6, 12, 18, and 24 months will be assessed.

  5. Total Cholesterol

    Time frame: 12, and 24 months

    Mean total cholesterol in both treatment groups at 12 and 24 months will be assessed.

  6. High Density Lipoprotein (HDL)

    Time frame: 12, and 24 months

    Mean HDL in both treatment groups at 12 and 24 months will be assessed.

  7. Low Density Lipoprotein (LDL)

    Time frame: 12, and 24 months

    Mean LDL in both treatment groups at 12 and 24 months will be calculated.

  8. Triglycerides

    Time frame: 12, and 24 months

    Mean triglycerides in both treatment groups at 12 and 24 months will be calculated.

Other outcomes

  1. Fasting Insulin

    Time frame: 6, 12, and 24 months

    Mean change in fasting insulin from baseline between treatment groups at 6, 12, and 24 months will be assessed.

  2. Homeostasis Model of Insulin Resistance (HOMA IR)

    Time frame: 6, 12, and 24 months

    Mean change in the HOMA IR model from baseline between treatment groups at 6, 12, and 24 months will be assessed.

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

Registry information

Official study title

Latinos Combatiendo la Diabetes (Latinos Combating Diabetes)

Acronym: La Comunidad

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Apr 15, 2013
Registry last updated
Aug 28, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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