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Feasibility of Reducing Cardiovascular Disease Risk Factors in Hispanics Through a Family-Based Community Intervention

Feasibility of Reducing Cardiovascular Disease Risk Factors in Hispanics Through a Family-Based Community Intervention

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05322876
Enrollment
80
Registered
2022-04-12
Start date
2022-03-22
Completion date
2024-12-31
Last updated
2024-04-03

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

Conditions

Cardiovascular Diseases, Metabolic Syndrome

Keywords

Metabolic Syndrome, Cardiovascular Disease Risk Factors, Community Intervention

Brief summary

The purpose of this study is to evaluate the feasibility of a 6-month family-based community intervention to mitigate cardiovascular disease risk factors in Hispanic families in northern Colorado as measured through biometric screenings, body composition, physical activity, and health knowledge.

Detailed description

The current project aims to leverage the UCHealth Healthy Hearts Family Program to provide a free, non-insurance-based 1-year cardiovascular disease (CVD) prevention and wellness program to Hispanic Colorado families. This program includes an interactive educational class series, baseline and quarterly biometric screenings, and optional consultations with an Exercise Physiologist and a Dietitian. This program takes a novel approach to preventative care by incorporating the family unit with the intention of having the child be the agent of change. The long-term goals of this project are to significantly improve CVD risk factors among participating families and to disseminate study findings to inform developing and current outreach programs to offer effective CVD prevention programs for Hispanic citizens. This work may ultimately lead to more Hispanics being served through new or existing programs, therefore expanding important preventative community health interventions into this underserved population.

Interventions

BEHAVIORALHealthy Hearts Family Program

Participants will participate in a baseline health and knowledge screening, followed by a 6-week once-weekly class series, and 3- and 6-month follow-up health and knowledge screenings.

Sponsors

Fitbit LLC
CollaboratorINDUSTRY
Poudre Valley Health System
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Sample

Eligibility

Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* At least one member of the family unit self-identifies as Hispanic * At least 13 years of age

Exclusion criteria

* Unwilling to wear Fitbit devices daily for 6 months except when charging and sleeping * Cannot read or understand either English or Spanish * Cannot return to screening location to perform the minimum of the baseline, 3-month and 6-month follow-up screenings * Children or adolescents will be excluded from this project without a minimum of one accompanying parent or guardian

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of program through changes in health knowledgeBaseline, post-6 week class series, 3- and 6-month follow-up appointments.Health knowledge gained and retained will be evaluated and compared at baseline, post-6 week class series, 3- and 6-month follow-ups utilizing previously developed and utilized Healthy Hearts knowledge survey. This outcome will be measured by correct responses on the Healthy Hearts knowledge survey.
Efficacy of program through changes in physical health - Body Composition - Fat MassBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBody composition (fat-free mass in pounds) measured with a Tanita MC980Uplus multi-frequency bio-electrical impedance analysis device.
Efficacy of program through changes in physical health - Body Fat PercentageBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBody composition (body fat percentage) measured with a Tanita MC980Uplus multi-frequency bio-electrical impedance analysis device.
Efficacy of program through changes in physical health - Visceral Fat RatingBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBody composition (Tanita visceral fat rating) measured with a Tanita MC980Uplus multi-frequency bio-electrical impedance analysis device.
Efficacy of program through changes in physical health - Daily StepsBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedPhysical activity metrics (daily average steps per month) measured by Fitbit devices
Efficacy of program through changes in physical health - Physical ActivityBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedPhysical activity metrics (daily minutes of light, moderate and vigorous activity per month) measured by Fitbit devices
Efficacy of program through changes in physical health - Blood PressureBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBiometric variables (blood pressure in mmHg)
Efficacy of program through changes in physical health - Lab Value -Lipid ProfileBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBiometric variables - lab values (lipid profile in mg/dL) measured through finger stick blood sampling
Efficacy of program through changes in physical health - Lab Value - TriglyceridesBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBiometric variables - lab values ( triglycerides in mg/dL) measured through finger stick blood sampling
Efficacy of program through changes in physical health - Lab Value - Blood GlucoseBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBiometric variables - lab values (blood glucose all in mg/dL) measured through finger stick blood sampling
Efficacy of program through changes in physical health - Waist CircumferenceBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBody composition (waist circumference in inches)
Efficacy of program through changes in physical health - Body Composition - Muscle MassBaseline, 3-month follow up and 6-month follow up data will be evaluated and comparedBody composition (muscle mass in pounds) measured with a Tanita MC980Uplus multi-frequency bio-electrical impedance analysis device.

Secondary

MeasureTime frameDescription
Adherence to program and utilization of additional resources - Fitbit UtilizationThese variables will be measured and assessed throughout the full 6 month program.Compliance to Fitbit utilization as measured by days worn throughout the 6 month program. The NHANES compliance to wear time of \> 10 hours worn per day will be utilized.
Adherence to program and utilization of additional resources - Resource UtilizationThese variables will be measured and assessed throughout the full 6 month program.Use of Exercise Physiologist and Dietician resources provided will be quantified and reported. This outcome will be reported as the number of consultation appointments requested and utilized throughout the program.
Adherence to program and utilization of additional resources - Program attendance - Percentage of Scheduled Visits AttendedThese variables will be measured and assessed throughout the full 6 month program.Attendance for screenings, classes and other consultations across baseline and follow-up visits. Attendance will be measured as the percentage of scheduled visits (including the 6 week class series and the 3- and 6-month follow-up visits) completed.

Countries

United States

Contacts

Primary ContactVictoria M Bandera, MS
victoria.bandera@uchealth.org7329913081
Backup ContactNaNet Jenkins, MPH
nanet.jenkins@uchealth.org9706245298

Outcome results

None listed

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