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临床试验/NCT01975181
NCT01975181终止不适用

Cardiovascular Health Program Registry

Walter Reed National Military Medical Center1 个研究点 分布在 1 个国家目标入组 1,164 人开始时间: 2014年12月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
1,164
试验地点
1
主要终点
Improvement in Cardiovascular Risk Score

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

Improvement in Cardiovascular Risk Score

时间窗: 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).

次要结局

  • 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)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (1)

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