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临床试验/NCT05897710
NCT05897710进行中(未招募)不适用

Virtual World-Based Cardiac Rehabilitation to Improve Cardiovascular Health and Outcomes Among Cardiac Patients

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 2,881 人开始时间: 2023年3月7日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Mayo Clinic
入组人数
2,881
试验地点
2
主要终点
Life's Essential 8 component: Self-Reported smoking status

研究概览

简要总结

The proposed trial is a multiphase, multicenter, non-inferiority, hybrid type 1 effectiveness, randomized controlled trial to test an innovative virtual world-based cardiac rehabilitation (CR) program, "Destination Cardiac Rehab". The primary objectives of this study are to assess the efficacy and adherence of "Destination Cardiac Rehab" compared to traditional center-based CR.

详细描述

The proposed virtual world-based cardiac rehabilitation (VWCR) program provides a novel home-based delivery method of a CR program to address several barriers to care associated with traditional center-based CR (CBCR). This 2-arm, randomized controlled trial (RCT) will rigorously assess adherence and efficacy of VWCR compared to CBCR in a 12-week (36-session) intervention that includes patient education, self-monitoring of physical activity and blood pressure, social support, and weekly telehealth visits with a CR nurse and exercise physiologist. Patients with a CR eligible cardiovascular event will be recruited from 6 geographically diverse CR centers across the United States. We hypothesize that the VWCR, known as "Destination Cardiac Rehab" will be non-inferior to CBCR as assessed by improvement in cardiovascular health and adherence to CR sessions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • Indication for CR according to Centers for Medicare & Medicaid Services (CMS) guidelines: Myocardial infarction within the preceding 12 months; Coronary artery bypass surgery; Current stable angina (chest pain); Heart valve repair or replacement; Percutaneous transluminal coronary angioplasty (PTCA) or coronary stenting; Heart or heart-lung transplant; Stable chronic heart failure
  • Aged ≥18 years
  • Basic Internet navigation skills
  • Active email address

排除标准

  • High risk patients according to the American Association of Cardiovascular and Pulmonary Rehabilitation (AACVPR) risk stratification (e.g., sudden cardiac arrest survivor)
  • Receiving continuous inotropic support
  • Presence of a mechanical circulatory support device
  • Decompensated heart failure
  • Symptomatic valvular heart disease
  • Uncontrolled angina
  • Presence of hemodynamically unstable dysrhythmias (e.g., ventricular tachycardia) given safety concern of unsupervised exercise20
  • Pregnant (due to associated hormonal and weight changes)
  • Non-English-speaking
  • Visual/hearing impairment or mental disability that would preclude independent use of the VW platform

结局指标

主要结局

Life's Essential 8 component: Self-Reported smoking status

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in smoking status using the National Health and Nutrition Examination Survey-Smoking-Cigarette Use Questionnaire (NHANES-SMQ), evaluating current and past smoking habits

Life's Essential 8 component: Cholesterol

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in Non-HDL Cholesterol levels reported as mg/dL

Life's Essential 8 component: Self-reported healthy diet

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in healthy diet using the Mediterranean Eating Patterns for Americans (MEPA), a 16-item questionnaire evaluating accordance with a Mediterranean-like diet pattern

Life's Essential 8 component: Sleep Quality

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in sleep quality (number of hours of sleep nightly) using the Pittsburg Sleep Quality Index (PSQI).

Life's Essential 8 component: Body Mass Index (BMI)

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in BMI as calculated with weight (kg) and height (m), reported as kg/m\^2

Life's Essential 8 component: Blood Glucose

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in Hemoglobin A1c (percent) and fasting blood glucose (mg/dL)

Life's Essential 8 component: Blood Pressure

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in systolic and diastolic blood pressure measurements; average of three sitting readings in mmHg

Life's Essential 8 component: Self-reported physical activity

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in physical activity using the International Physical Activity Questionnaire (IPAQ), a 12-item questionnaire classifying physical activity as "low," "moderate," or "high" intensity physical activity (minutes/day) over the prior week

Life's Essential 8 composite score: Cardiovascular health

时间窗: Baseline, 3 months, and 6 months post-randomization

Changes from baseline in Life's Essential 8 score. Life's Essential 8 composite score is determined as a composite of all components by calculating an unweighted average score on a scale of 0 to 100 points. An overall cardiovascular health score (Life's Essential 8 score) will be considered high (80 to 100 points), moderate (50 to 79 points) or low for (0 to 49 points).

Number of sessions attended by participants

时间窗: Baseline through 12-week program

Optimal adherence defined as completion of 70% or more of weekly visits (in-person or virtual). Attendance measured by CR staff for control group, and by VWCR web administrators, Exercise Physiologists, and Nurse Coaches in the VWCR arm.

次要结局

  • Physical Activity Social Support(Baseline, 3 months, and 6 months post-randomization)
  • MACE (Major Adverse Cardiovascular Events) 3 months post-randomization(3 months and 6 months post-randomization)
  • Functional Capacity(Baseline, 3 months, and 6 months post-randomization)
  • Physical Activity Self-efficacy(Baseline, 3 months, and 6 months post-randomization)
  • Diet Self-efficacy(Baseline, 3 months, and 6 months post-randomization)
  • Exercise Sessions(Baseline through 12-week (36 session) cardiac rehabilitation program)
  • Physical Activity Self-regulation(Baseline, 3 months, and 6 months post-randomization)
  • Diet Self-regulation(Baseline, 3 months, and 6 months post-randomization)
  • Health-related quality of life(Baseline, 3 months, and 6 months post-randomization)
  • Diet Social Support(Baseline, 3 months, and 6 months post-randomization)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

LaPrincess C. Brewer

Associate Professor of Medicine

Mayo Clinic

研究点 (2)

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