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Clinical Trials/NCT01975181
NCT01975181
Terminated
Not Applicable

Cardiovascular Health Program Registry

Walter Reed National Military Medical Center1 site in 1 country1,164 target enrollmentDecember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Disease
Sponsor
Walter Reed National Military Medical Center
Enrollment
1164
Locations
1
Primary Endpoint
Improvement in Cardiovascular Risk Score
Status
Terminated
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to establish a registry that uses observational study methods to collect uniform data (clinical, lifestyle and other) to evaluate specific outcomes and to enable research on patients at risk for cardiovascular disease (CVD).

This is a descriptive, observational registry study. All data for participants in the WRNMMC Integrative Cardiac Health Project (ICHP) Cardiovascular Health Program (CHP) will be entered into a single, secure information management system (IMS) for subjects at risk for CVD. At periodical intervals, the IMS will be queried to define the effect of an integrative therapeutic lifestyle change (TLC) program on CVD risk over time. This protocol outlines collection, storage, and handling of data, describes specific data elements and lays the foundation for future research questions.

Detailed Description

The CHP registry consists of uniform data to evaluate the outcomes of military beneficiaries at CVD risk. These uniform data include variables (clinical, lifestyle, traditional, non-traditional, objective and subjective) that are used to assess a CVD risk profile and the effects of TLC. All data are collected in the course of the clinical CHP. Data are comprised of demographic information; past and intercurrent medical history including risk factors of CVD such as coronary artery disease (CAD), carotid disease, peripheral arterial disease, aortic aneurysm hypertension, diabetes and sleep apnea; smoking, alcohol and drug use history; family history of CVD and other chronic diseases; deployment history, injuries and occupational exposures; mental health history including PTSD, depression and anxiety; lifestyle information comprised of self-reported dietary patterns, exercise activities, stress levels, and sleep habits; physical examination including vital signs, body mass index, waist circumference and per cent body fat; laboratory data routinely requested by the CHP for risk assessment of all patients entering the program is comprised of total cholesterol, cholesterol fractions, fasting glucose, fasting insulin, hemoglobin A1C, highly sensitive C-reactive protein, and vitamin D levels; and CV diagnostic tests such as EKG, echocardiogram, cardiac stress testing; and sleep testing. Data are measured at baseline (CHP enrollment), completion of onsite CHP (6 months) and after follow-up of the telephonic coaching phase (approximately 1 year). Data may also be collected annually for up to 5 years if available.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
August 24, 2017
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Any adult military, DEERS eligible, beneficiary who is participating in the CHP.
  • Subjects who present to the CHP for evaluation and participation may be self-referred or be referred by a provider.
  • Must have working email address and access to the internet.
  • Participants elect to enroll in order to learn about healthy lifestyle choices that can help prevent the development of cardiovascular disease.

Exclusion Criteria

  • Less than 18 years of age.
  • Individuals unable or unwilling to participate or give informed consent will be excluded from registry enrollment.
  • Subjects who were part of the retrospective CHP cohort cannot be enrolled in the prospective study.

Outcomes

Primary Outcomes

Improvement in Cardiovascular Risk Score

Time Frame: 8 months

A cardiovascular risk score is calculated using the Framingham Risk Score PLUS other factors including family history, body mass index, diastolic blood pressure, high sensitivity C-reactive protein, low-density lipoprotein, triglyceride and lipoprotein (a).

Secondary Outcomes

  • Improvement in Dietary Score using the Rate-Your Plate Dietary Assessment Tool(8 months)
  • Improvement in Perceived Stress Scale(8 months)
  • Improvement in Exercise(8 months)
  • Improvement in Pittsburgh Sleep Quality Index (PSQI)(8 months)

Study Sites (1)

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