Strong Hearts for New York is a research study which aims to reduce cardiovascular disease (CVD), improve quality of life, and reduce CVD related health care costs in rural communities. Our aim is to better understand how changes in lifestyle can affect the health of rural women and others in their communities.
There are notable cardiovascular disease (CVD) disparities among people living in rural settings, particularly medically underserved rural areas. Complex factors such as socioeconomic disadvantage, social and cultural dynamics, geographic distances/barriers, and limited access to healthcare, healthy foods, and/or physical activity opportunities contribute to the issue. The objective of Strong Hearts, Healthy Communities (SHHC) is to reduce rural CVD disparities through civic engagement and implementation of a community-based intervention in 11 underserved New York communities. SHHC builds upon a long-standing collaboration with National Institute of Food and Agriculture cooperative extension educators, who will implement the project. There is limited knowledge about how programs and services can move beyond commonly used individual-level approaches-which have limitations in terms of cost, impact, reach, and sustainability-to effectively reduce rural CVD health disparities using an integrated, multi-level, community-engaged approach. The objective of Strong Hearts, Healthy Communities (SHHC) is to address this gap in knowledge and practice by working with residents, practitioners, health educators, local leadership, and other stakeholders in 11 medically underserved rural communities in New York to test a comprehensive program designed to: a) improve diet and physical activity behaviors, b) promote local built environment resources, and c) shift social norms about active living and healthy eating through civic engagement, capacity building, and community based programming. RANDOMIZED INTERVENTION AND DELAYED INTERVENTION: In the current phase of the project, the efficacy of the SHHC program curriculum will be evaluated in a 24-week delayed intervention trial. The investigators will compare changes in CVD-related anthropometric, physiologic, behavioral, and psychosocial parameters between subjects in 5 intervention and 6 delayed communities in New York State. In addition, changes in behavior, attitudes, and knowledge among SHHC intervention subjects' "social network" will be evaluated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
182
The investigators will evaluate the efficacy of the SHHC curriculum in a 24-week community-based randomized delayed intervention trial. They will compare changes in CVD-related anthropometric, physiologic, behavioral, and psychosocial parameters between subjects in 5 intervention and 6 delayed intervention communities. In addition, the investigators will evaluate changes in behavior, attitudes, and knowledge among SHHC intervention subjects' "social network".
The investigators will evaluate the efficacy of the SHHC curriculum in a 24-week community-based randomized delayed intervention trial. They will compare changes in CVD-related anthropometric, physiologic, behavioral, and psychosocial parameters between subjects in 5 intervention and 6 delayed intervention communities. In addition, the investigators will evaluate changes in behavior, attitudes, and knowledge among SHHC intervention subjects' "social network".
Clyde
Clyde, New York, United States
Cobleskill
Cobleskill, New York, United States
Cooperstown
Cooperstown, New York, United States
Change in body weight
Time frame: Baseline to 24 weeks
Changes in body weight
Time frame: Baseline to 48 weeks
Changes in blood pressure
Time frame: Baseline to 24 weeks, 48 weeks
Changes in blood lipids
Time frame: Baseline to 24 weeks, 48 weeks
Changes in c-reactive protein
Time frame: Baseline to 24 weeks, 48 weeks
Changes in hemoglobin A1C
Time frame: Baseline to 24 weeks, 48 weeks
Changes in waist circumference
Time frame: Baseline to 24 weeks, 48 weeks
Changes in hip circumference
Time frame: Baseline to 24 weeks, 48 weeks
Changes in 7 day accelerometry
Time frame: Baseline to 24 weeks, 48 weeks
Changes in 7 day dietary recall
Time frame: Baseline to 24 weeks, 48 weeks
Changes in healthy eating self-efficacy assessed by questionnaire
Time frame: Baseline to 24 weeks, 48 weeks
Changes in exercise self-efficacy assessed by questionnaire
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Dolgeville and Little Falls
Dolgeville, New York, United States
Hamilton
Hamilton, New York, United States
Hartwick
Hartwick, New York, United States
Herkimer, Mohawk and Ilion
Herkimer, New York, United States
Ithaca
Ithaca, New York, United States
Seguin Research Lab, Cornell University
Ithaca, New York, United States
Milford
Milford, New York, United States
...and 3 more locations
Time frame: Baseline to 24 weeks, 48 weeks
Changes in healthy eating attitudes of social network of participants assessed by questionnaire
Time frame: Baseline to 24 weeks, 48 weeks
Changes in exercise attitudes of social network of participants assessed by questionnaire
Time frame: Baseline to 24 weeks, 48 weeks
Changes in healthy eating self-efficacy of social network of participants assessed by questionnaire
Time frame: Baseline to 24 weeks, 48 weeks
Changes in exercise self-efficacy of social network of participants assessed by questionnaire
Time frame: Baseline to 24 weeks, 48 weeks