Improving Heart Health in Appalachia (HeartHealth)
Primary Purpose
Obesity, Hypertension, Hyperlipidemia
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-care CVD risk reduction
Referral to primary care provider for CVD risk management
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring lifestyle change, behavior change, obesity, hypertension, hyperlipidemia, physical inactivity, depression
Eligibility Criteria
Inclusion Criteria:
- residents of eastern Appalachian Kentucky
- do not have a primary care provider
at risk for CVD as reflected by having two or more of the following modifiable risk factors
- clinical diagnosis of hypertension or taking medications diagnosed for hypertension or found to be hypertensive on screening;
- clinical diagnosis of hyperlipidemia or taking medication for treating abnormal lipid levels, or any lipid abnormality found on screening that indicates hyperlipidemia;
- diagnosis of type 2 diabetes or HgA1c > 7% found on screening;
- overweight or obese (body mass index ≥ 25 kg/m2);
- waist circumference > 40 inches in men or > 35 inches in women;
- clinical diagnosis of depression, on medications for depression or found to have depressive symptoms (score of > 9 on the Patient Health Questionnaire-9) by baseline screening;
- sedentary lifestyle meaning that the individual does not engage in at least 30 minutes of moderate activity for at least 4 days per week
Exclusion Criteria:
- known coronary artery disease, cerebrovascular disease, history of acute coronary syndrome or peripheral arterial disease;
- taking medications (e.g., protease inhibitors) that interfere with lipid metabolism;
- cognitive impairment that precludes an individual from understanding the consent process, answering questionnaires, or participating in the intervention;
- chronic drug abuse;
- end-stage renal or liver or pulmonary disease;
- current active cancer (i.e., undergoing active treatment for cancer) other than isolated skin cancer treatable by simple excision;
- gastrointestinal disease that requires special diets (e.g., Crohn's disease; celiac disease)
Sites / Locations
- University of Kentucky
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Self-care CVD risk reduction
Referral to primary care provider
Arm Description
A patient-centered, culturally appropriate lifestyle approach to promoting self-care in high risk patients.
The study team provides a primary care provider for the patient, makes the referral and sends appropriate CVD risk reduction guidelines to the provider.
Outcomes
Primary Outcome Measures
cardiovascular risk factor selected by patient
Patient selects their own risk reduction goal from the following:
smoking, blood pressure, lipid profile, body mass index, hemoglobin-A1c for diabetics, depression, physical activity level, waist circumference
cardiovascular risk factor selected by patient
Patient selects their own risk reduction goal from the following:
smoking, blood pressure, lipid profile, body mass index, hemoglobin-A1c for diabetics, depression, physical activity level, waist circumference
Secondary Outcome Measures
all CVD risk factors of each patient
All CVD risk factors that each patient has are secondary outcomes
all CVD risk factors of each patient
All CVD risk factors that each patient has are secondary outcomes
Full Information
NCT ID
NCT01884246
First Posted
June 14, 2013
Last Updated
March 7, 2017
Sponsor
Debra Moser
Collaborators
University of Kentucky Center for Excellence in Rural Health-Hazard
1. Study Identification
Unique Protocol Identification Number
NCT01884246
Brief Title
Improving Heart Health in Appalachia
Acronym
HeartHealth
Official Title
Reducing Health Disparities in Appalachians With Multiple Cardiovascular Disease Risk Factors
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
August 1, 2013 (Actual)
Primary Completion Date
December 31, 2016 (Actual)
Study Completion Date
December 31, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Debra Moser
Collaborators
University of Kentucky Center for Excellence in Rural Health-Hazard
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Individuals in Appalachian Kentucky are vulnerable to cardiovascular disease (CVD) by virtue of having high rates of multiple CVD risk factors. There is a critical need to develop and test CVD risk reducing interventions that are appropriate and effective in Appalachia. In the absence of such interventions, the dramatic CVD disparities seen in this area will continue to rise.
Lifestyle interventions reduce CVD risk by 44%. The investigators and others have demonstrated that lifestyle change is most effective when patients are given the tools to engage in effective self-care, and that interventions individualized to patients' specific needs and barriers are more effective than interventions that are not. The central hypothesis is that to be successful in Appalachia, CVD risk reducing interventions must focus on patient-centered lifestyle change that increase individuals' abilities to engage in self-care, must be culturally appropriate, and must have components that overcome barriers faced by individuals living in Appalachia.
The investigators propose a randomized, controlled comparative effectiveness trial with 300 individuals from Appalachian Kentucky who do not have a primary care provider and who are at risk for CVD by virtue of having two or more modifiable CVD risk factors. The investigators will compare (1) a patient-centered, culturally appropriate, self-care CVD risk reduction intervention (HeartHealth) designed to improve multiple CVD risk factors while overcoming barriers to success with (2) referral of patients to a primary care provider for management of their CVD risk factors. The investigators propose the following specific aims to be tested at 4 months and 1 year after baseline. To compare the short and long-term impact of the interventions on:
1) the risk factor selected by patients (i.e., tobacco use, blood pressure, lipid profile, hemoglobin-A1c (HgA1c) for diabetics, body mass index, waist circumference, depressive symptoms, or physical activity level); 2) all of the CVD risk factors of each patient; 3) quality of life; 4) patient and healthcare provider satisfaction; 5) desirability and adoptability by assessing adherence to recommended CVD risk reduction measures, and retention of recruited individuals. The investigators hypothesize that in comparison to the referral strategy, the multifaceted patient-centered, self-care intervention will engender more favorable outcomes across all measures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Hypertension, Hyperlipidemia, Depression
Keywords
lifestyle change, behavior change, obesity, hypertension, hyperlipidemia, physical inactivity, depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
330 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Self-care CVD risk reduction
Arm Type
Experimental
Arm Description
A patient-centered, culturally appropriate lifestyle approach to promoting self-care in high risk patients.
Arm Title
Referral to primary care provider
Arm Type
Active Comparator
Arm Description
The study team provides a primary care provider for the patient, makes the referral and sends appropriate CVD risk reduction guidelines to the provider.
Intervention Type
Behavioral
Intervention Name(s)
Self-care CVD risk reduction
Other Intervention Name(s)
HeartHealth
Intervention Description
A patient-centered, culturally appropriate lifestyle approach to promoting self-care in high risk patients.
Intervention Type
Other
Intervention Name(s)
Referral to primary care provider for CVD risk management
Intervention Description
The study team provides a primary care provider for the patient, makes the referral and sends appropriate CVD risk reduction guidelines to the provider.
Primary Outcome Measure Information:
Title
cardiovascular risk factor selected by patient
Description
Patient selects their own risk reduction goal from the following:
smoking, blood pressure, lipid profile, body mass index, hemoglobin-A1c for diabetics, depression, physical activity level, waist circumference
Time Frame
4 months
Title
cardiovascular risk factor selected by patient
Description
Patient selects their own risk reduction goal from the following:
smoking, blood pressure, lipid profile, body mass index, hemoglobin-A1c for diabetics, depression, physical activity level, waist circumference
Time Frame
12 months
Secondary Outcome Measure Information:
Title
all CVD risk factors of each patient
Description
All CVD risk factors that each patient has are secondary outcomes
Time Frame
4 months
Title
all CVD risk factors of each patient
Description
All CVD risk factors that each patient has are secondary outcomes
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
quality of life
Time Frame
4 months
Title
quality of life
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
residents of eastern Appalachian Kentucky
do not have a primary care provider
at risk for CVD as reflected by having two or more of the following modifiable risk factors
clinical diagnosis of hypertension or taking medications diagnosed for hypertension or found to be hypertensive on screening;
clinical diagnosis of hyperlipidemia or taking medication for treating abnormal lipid levels, or any lipid abnormality found on screening that indicates hyperlipidemia;
diagnosis of type 2 diabetes or HgA1c > 7% found on screening;
overweight or obese (body mass index ≥ 25 kg/m2);
waist circumference > 40 inches in men or > 35 inches in women;
clinical diagnosis of depression, on medications for depression or found to have depressive symptoms (score of > 9 on the Patient Health Questionnaire-9) by baseline screening;
sedentary lifestyle meaning that the individual does not engage in at least 30 minutes of moderate activity for at least 4 days per week
Exclusion Criteria:
known coronary artery disease, cerebrovascular disease, history of acute coronary syndrome or peripheral arterial disease;
taking medications (e.g., protease inhibitors) that interfere with lipid metabolism;
cognitive impairment that precludes an individual from understanding the consent process, answering questionnaires, or participating in the intervention;
chronic drug abuse;
end-stage renal or liver or pulmonary disease;
current active cancer (i.e., undergoing active treatment for cancer) other than isolated skin cancer treatable by simple excision;
gastrointestinal disease that requires special diets (e.g., Crohn's disease; celiac disease)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Debra K Moser, DNSc, RN
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Kentucky
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40535
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Improving Heart Health in Appalachia
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