CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 182 enrolled
Drug / intervention
Group 1 (Intervention) +1 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03059472
NCT03059472N/ACompleted
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Strong Hearts for New York: A Rural Community CVD Prevention Program

Cornell University·interventional·Posted Feb 23, 2017·Updated Jan 5, 2022

In Brief

A clinical study evaluating Group 1 (Intervention) and Group 2 (Delayed intervention) for Heart Disease and 4 related conditions. Completed, enrolled 182 participants across 13 sites.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHeart Disease, Cardiovascular Disease, Sedentary Lifestyle, Overweight, Obesity
CountriesUnited States
CollaboratorsMontana State University, Tufts University, Bassett Healthcare, Cornell Cooperative Extension

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedFeb 23, 2017
Enrollment StartMar 31, 2017
Primary CompletionFeb 28, 2019
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 9.4 years ago

Interventions

Group 1 (Intervention)behavioral

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".

Group 2 (Delayed intervention)behavioral

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".