Tailoring Mobile Health Technology to Reduce Obesity and Improve Cardiovascular Health in Resource-Limited Neighborhood Environments
Obesity
About this trial
This is an interventional basic science trial for Obesity focused on measuring Community-Based Participatory Research, Obesity, Cardiovascular Disease Risk, Social Determinants of Health
Eligibility Criteria
- INCLUSION CRITERIA:
Individuals eligible for this protocol are overweight or obese (BMI greater than or equal to 25 kg/m2) African American women aged 21-75 years who live in Washington, DC Wards 5,7, or 8 and neighboring areas of Prince George s County, MD. Eligible participants
should also have access to a smartphone compatible with the mobile app for the protocol that they can use for the study. Eligible participants must be able to provide informed consent independently and also speak and read English at the 8th grade level.
EXCLUSION CRITERIA:
- Medical condition, including recent unintentional weight loss, that might prohibit safe participation in the intervention
- Heart disease as indicated by history of myocardial infarction, documented obstructive coronary artery disease on coronary angiography, coronary artery stent placement, congestive heart failure, significant structural heart disease (e.g. hypertrophic or dilated cardiomyopathy, valvular heart disease)
- Physically unable to perform the physical activity for any reason
- Pregnant women due to large hormonal changes during pregnancy that affect study variables and potential pregnancy-related restrictions on exercise. Self-reported pregnancy status will be accepted.
Pilot Study INCLUSION CRITERIA:
- Must be an African-American female
- Must be within the age of 21-75 years old
- Must be overweight or obese (Body Mass Index (BMI) greater than or equal to 25 kg/m <=)
- Must live in Washington DC Wards (5, 7, or 8) or live in Prince George s County, Maryland.
- Must have a smartphone that is compatible with the study software (mobile app)
- Must be willing to use the software on personal smartphone for the study
- Must be able to provide consent
- Must be willing to wear the wrist-worn physical activity device for the study
- Must not be pregnant
Sites / Locations
- National Institutes of Health Clinical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Other
Other
Group 2 Label: PA monitor with standard remote coaching (SRC)
Group 1 Label: PA monitor with remote coaching tailored to place
African American women who are at risk for cardiovascular outcomes in resource-limited communities in the Washington D.C. area.
African American women who are at risk for cardiovascular outcomes in resource-limited communities in the Washington D.C. area.