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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01439477
Other study ID # TuftsU-9289
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2013
Est. completion date November 2015

Study information

Verified date April 2024
Source Tufts University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardiovascular disease (CVD) is the leading cause of death for women in the United States. CVD disproportionately affects underserved populations, specifically low-income, minority, and rural women who have higher obesity rates and experience other health disparities. There is a need for replicable, evidence-based programs that target women, particularly midlife and older women who represent an increasing proportion of the U.S. population, to reduce their CVD risk . StrongWomen - Healthy Hearts is a 12-week, community-based program that has demonstrated effectiveness at improving CVD risk factors, including body weight, diet quality, and physical activity in a controlled, randomized trial conducted with midlife and older overweight and obese subjects in Arkansas and Kansas. The central objective is to rigorously evaluate dissemination of the StrongWomen - Healthy Hearts Program using the RE-AIM framework to achieve maximal public health impact. Expanded dissemination will occur through the Cooperative State Research, Education and Extension Service (CSREES) This partnership will leverage a long and successful collaboration between Tufts University and CSREES that provides strength training programs to older women in 41 states.


Recruitment information / eligibility

Status Completed
Enrollment 763
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years and older
Eligibility Inclusion Criteria: - Greater than 40 years of age - Female - BMI greater than 24 - sedentary (not doing any type of exercise more than once per week) Exclusion Criteria: - unstable medical condition that would preclude participation in an exercise program - current participation in another lifestyle modification program - cognitive impairment - pregnancy.

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tufts University

Outcome

Type Measure Description Time frame Safety issue
Other Adherence 9/2014-7/2015
Other Retention 9/2014-7/2015
Other Satisfaction with Intervention 4/2014-7/2015
Primary Body Weight 9/2014-7/2015
Secondary Waist circumference 9/2014-7/2015
Secondary Percent Body Fat 9/2014-7/2015
Secondary Diet (24-hour recall) 9/2014-7/2015
Secondary Physical Activity (IPAQ) 9/2014-7/2015
Secondary Physical Activity (accelerometer) 9/2014-7/2015
Secondary Cardiorespiratory Fitness (1-Mile Walk Test) 9/2014-7/2015
Secondary Blood Pressure 9/2014-7/2015
Secondary Self-Regulation 9/2014-7/2015
Secondary Collective Efficacy 9/2014-7/2015
Secondary Perceived Stress 9/2014-7/2015
Secondary Self-Efficacy 9/2014-7/2015
Secondary Perceived Social Support 9/2014-7/2015
Secondary Civic Engagement 9/2014-7/2015
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