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NCT Number: NCT06517459

Cultural Modification of an Evidence Based Healthy Lifestyle Intervention for People Post Stroke Who Identify as Hispanic/Latino

The purpose of this trial is to examine weight loss for Hispanic/Latino people with stroke (CVA) who take part in a healthy lifestyle program that has been culturally modified for Hispanic/Latino people

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Baylor Institute for Rehabilitation

Dallas, Texas, 75246, United States

Location status: Recruiting

Location contact

Alvaro Carrera

CONTACT

[email protected]

4698315321

About this study

Weight gain greatly increases the risk of chronic diseases such as diabetes, metabolic syndrome, pulmonary and heart disease. The Group Lifestyle Balance (GLB) intervention is a 12-month, evidence-based weight-loss program that has been used extensively with the general population and with people after CVA, however, it is not adapted to be linguistically and culturally appropriate for Latino persons post stroke. We will modified the program to meet the needs of Latino people with a CVA (GLB-CVA Latino).

Aims:

  • : To create a modification of the CDC-recognized, evidence-based GLB-CVA to be culturally appropriate to meet the unique needs of people who identify as Hispanic/Latino, available in English and Spanish languages, using a Community-Based Participatory Research approach and AB of key stakeholders (patients, caregivers, clinicians, researchers).
  • : Conduct a single-arm trial to describe the effect of participation in the GLB-CVA Latino on primary and secondary outcomes for 24 individuals who identify as Hispanic/Latino (12 English speakers and 12 Spanish speakers) at 3, 6, and 12 months from baseline.
  • : Evaluate the participant compliance (feasibility) and fidelity (adherence to the DPP GLB content) with the GLB-CVA Latino intervention.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • BMI ≥25
  • Identify as Hispanic or Latino
  • 18-85 years of age
  • All types of stroke
  • Medically able to participate in a weight-loss program
  • Physical Activity Readiness Questionnaire +
  • ≥12 months post first stroke

Exclusion criteria

  • Contraindications for physical activity
  • Low Cognitive Function
  • Residing in hospital, acute rehab, SNF
  • Not fluent in English or Spanish
  • Pre-existing eating disorder
  • Pregnancy

Treatment and study plan

Group Lifestyle Balance

Behavioral

The Group Lifestyle Balance (GLB) program is a self-management intervention that has been shown to result in weight-loss and reduce the risk for Type 2 diabetes through increased physical activity and healthy eating behaviors in the general population. The GLB is a direct adaptation of the Diabetes Prevention Program, both developed at the Diabetes Prevention and Support Center at the University of Pittsburgh. The GLB is designed for delivery in a group-based, community setting,4 and has resulted in weight-loss in a variety of settings, such as community centers, churches, worksites, and healthcare systems.

Primary outcomes

  1. Change in weight

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Weight will be measured during in-person assessments at BSWIR using a Seca 664 scale. Height will be measured using a stadiometer. Weight and height will be used to calculate BMI. A BodyTrace Smart Scale will be provided to participants to facilitate self-weighing in the home, which include cellular connectivity at no cost to participants so weight will be sent directly to the research team.

Secondary outcomes

  1. HbA1c

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Fasting venous sample will be obtained for hemoglobin a1c to assess average blood sugar level over the past 2-3 months. Fasting venous samples will also be collected for fasting blood glucose, HDL/LDL, total cholesterol, and triglyceride level. Coordinators are trained phlebotomists

  2. Fasting blood glucose

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Fasting venous sample will be obtained for hemoglobin a1c to assess average blood sugar level over the past 2-3 months. Fasting venous samples will also be collected for fasting blood glucose, HDL/LDL, total cholesterol, and triglyceride level. Coordinators are trained phlebotomists

  3. Lipid panel

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Fasting venous sample will be obtained for hemoglobin a1c to assess average blood sugar level over the past 2-3 months. Fasting venous samples will also be collected for fasting blood glucose, HDL/LDL, total cholesterol, and triglyceride level. Coordinators are trained phlebotomists

  4. Circumference

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Waist circumference measured at the umbilicus and mid-upper arm circumference following ACSM guidelines.

  5. Height

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Will be collected using a stadiometer and used to calculate BMI

  6. Blood pressure

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Using an automatic cuff (average of three readings, patient seated) diastolic and systolic scores will be recorded

  7. 8-year Diabetes Risk

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    The Framingham Heart Study diabetes risk score83 will be calculated using predictors including age, gender, fasting glucose, BMI, HDL cholesterol and triglyceride levels, blood pressure, and parental history. Risk score calculator and regression model are free and used in GLB weight-loss trials. The age range for this score is 45 years to 64 years, and therefore only individuals within this age will have calculated scores. Furthermore, the minimum cut-off score is 3.

  8. 6 Minute Walk Test (6MWT)

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Assesses distance walked over 6 minutes as a sub-maximal test of aerobic capacity.

  9. 10 Meter Walk Test (10MWT)

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Assesses walking speed in (m/s) which is correlated to mobility in the community, capacity to perform ADLs, risk of falls, re-hospitalization, and risk of cognitive decline.

  10. Behavioral Risk Factor Surveillance System (BRFSS)

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    The BRFSS is a state-based system of health surveys that collects information on health risk behaviors, preventative health practices, and health care access primarily related to chronic disease and injury. The GLB-TBI uses the two subscales of Healthy Eating and Physical Activity from the 2017 version of the BRFSS. It consists of 14 items.

  11. Neighborhood Environment Walkability Scale (NEWS)

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    NEWS assesses participants' perception of neighborhood features related to physical activity and grocery shopping, including residential density, land use mix (including both indices of proximity and accessibility), street connectivity, infrastructure for walking/cycling, neighborhood aesthetics, traffic and crime safety, and neighborhood satisfaction.

  12. Short Assessment of Health Literacy

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Combined word recognition test and comprehension test using multiple-choice questions. Identifies individuals with low health literacy.

  13. Self-Rated Abilities for Health Practice

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Includes 28 items to assess health behaviors among people with disabilities and yields a total Health Practices Score plus 4 subscale scores (Exercise, Nutrition, Health Practices, and Psychological Well Being). Items are rated on a 5-point scale from 0 'not at all' to 4 'completely.' Scores range from 0-28 with higher scores indicating higher self-efficacy for the health behaviors.

  14. Stroke Impact Scale - Quality of Life

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Quality of life will be assessed using the Stroke Impact Scale, which assesses 8 dimensions of health-related quality of life specific to people post stroke including subscales (using a 5pt Likert scale) assessing strength, memory and thinking, emotion, communication, activities of daily living, mobility, hand function, and participation/role function.

  15. Change in Exit Survey

    Time frame: [Time Frame: 12 months]

    Participants will be asked to complete an exit survey at the 12-month assessment, asking about experience in, and satisfaction with, the GLB-CVA Latino (including satisfaction and feasibility with modifications and language translation) and suggestions for improvement.

  16. Brief Acculturation Scale for Hispanics

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    4 item language based measure of acculturation for Hispanic populations.

  17. Social Support for Eating Habits

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Questionnaire that assesses the frequency of support received from others for healthy eating habits over the past 3 months.

  18. Social Support for Physical Activity

    Time frame: [Time Frame: Baseline, 3, 6, and 12 months]

    Questionnaire that assesses the frequency of support received from others for engaging in physical activity over the past 3 months

Study contacts

Contact information is provided by the study sponsor or research team.

Alvaro Carrera

CONTACT

[email protected]

469-831-5321

Sponsors and collaborators

Lead sponsor

Baylor Research Institute

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 24, 2024
Registry last updated
Oct 15, 2025

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

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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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