Comprehensive 12-week Lifestyle Change Program in Elderly Patients With Heart Failure
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 34
- 试验地点
- 2
- 主要终点
- Functional status as measured by handgrip strength.
研究概览
简要总结
Summary
Chronic heart failure continues to be one of the highest economic burdens in the United States, heavily influenced by frequent readmissions to the hospital. This study will examine whether patients 65 years and older, who have NYHA class II and III heart failure, will improve their symptoms after participating in a comprehensive 12-week lifestyle change program. The investigators will recruit potential subjects primarily from the Scripps Clinic heart failure clinic at the Torrey Pines campus. Qualifying subjects will be randomized to medical treatment as usual or the lifestyle program. The investigators will enroll 17 subjects into each group which will provide 80% power and an alpha of 0.05.
The lifestyle change program consists of classes conducted three times a week for 12 weeks at the Scripps Center for Integrative Medicine. Each day participants will spend about four to five hours in a variety of classes such as monitored exercise, group support, mindful-yoga and meditation, vegetarian cooking classes, music-centered wellness, mind-body lectures, and resiliency training.
The primary outcomes will focus on determining functional status and physical agility using the 6-minute walk test, handgrip strength, and NYHA class categories. In addition, the investigators will capture subjective physical status with a self-reported questionnaire. Cognitive assessment will be performed using the Montreal Cognitive Assessment tool. To capture the subject's overall self-reported improvement the investigators will use a quality of life and a depression questionnaire. Secondary endpoints include hospital admission rates and all-cause mortality.
详细描述
The investigators Research Question and Hypothesis is as follows:
Comprehensive, evidence-based lifestyle and psychosocial interventions over a 12-week period (Lifestyles Change Program) can improve various objectives (6-minute walk distance, Left Ventricular Ejection Fraction (LVEF), New York Heart Association Class, grip strength, and cognitive function) as well as subjective (Quality of life, depression and functional screening) measures in patients with chronic heart failure. Secondary endpoints would include data such as hospital admission rates and all-cause mortality.
Background/ Gaps in Knowledge Chronic heart failure continues to be one of the highest economic burdens in the United States, heavily influenced by frequent readmissions. As a measure of performance quality, the Center of Medicare and Medicaid Services (CMS) began publically reporting hospital risk-standardized 30-day all-cause readmission rates, among fee-for-service beneficiaries discharged after hospitalization for heart failure from all the US acute care hospitals (1). Previous reported averages for hospital readmission in patients with chronic heart failure averages 25% to 30%, with some studies showing a readmission rate of up to 45% at 6 months.
There has been significant research examining various methods to reduce hospital admissions and improve functional capacity for patients with heart failure. Aside from published data on patient factors associated with readmission (age, sex, race, education, diabetes, renal disease, history of stroke, cognitive impairment, New York Heart Association (NYHA) class level, and serum markers [blood urea nitrogen, creatinine, C-reactive protein], etc), there have been many prospective studies evaluating readmission rates in CHF using interventions including: specialized multi-disciplinary teams (CHF nursing staff, pharmacists, physicians, etc), telephonic home monitoring, implantable device monitoring, various exercise programs (intermittent vs. continuous), meditation and spirituality, and early hospital follow-up.
Attempts at creating valid statistical models to predict patients at the highest risk for readmission used heterogeneous approaches and found substantial inconsistencies regarding which patient characteristics were predictive. From a policy perspective, as of 2009, a validated risk-standardized model to accurately profile hospitals using readmission rates is unavailable in the published English-language literature to date (3). Essentially, the identification of patients at high risk for heart failure readmission remains difficult with no validated objective assessment. Therefore, the strategy to reduce readmissions of heart failure patients is evolving to become a more personalized, patient-centered approach based on specific needs of each patient. For example, studies evaluating patient vs physician and healthcare staff perceptions for the causes of heart failure readmissions (using standardized questionnaires), shows discrepancy in the physician's opinion vs the patient's opinion about what factors influenced the readmission.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
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
- 否
入选标准
- •Male or female, over 18
- •Able to commit to participating in the Lifestyle Change Program:
- •4 -5 hours per day
- •3 days per week
- •for a total of 12-weeks
- •History of CHF with systolic dysfunction (EF <45%) OR History of heart failure with preserved ejection fraction (HFpEF)
- •Must have had one previous admission for acute decompensated heart failure within the past year at time of enrollment.
- •New York Heart Association (NYHA) Class II - III symptoms:
- •Class II: Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity.
- •Class III: Marked limitation in activity due to symptoms, even during less-than- ordinary activity, e.g. walking short distances (20-100 m). Comfortable only at rest.
- •Labs: Complete Blood Count, Comprehensive Metabolic Panel must have been stable within the last 3 month.
- •Exercise: must be able to do some gentle exercises
- •Severe medical condition(s) that preclude participation in the Lifestyle Change Program
- •Unable to travel to the Scripps Center for Integrated Medicine Gym 3 times a week for 12 weeks
- •Severe cognitive, language, and psychosocial disabilities that prevent participation in the Lifestyle Change Program
- •Unsafe to participate in the exercise program based on the American College of Sports Medicine safety criteria such as:
- •Refractory chest pain
- •poorly controlled arrhythmias causing hemodynamic symptoms
- •high degree Atrioventricular block
- •pacemakers which do not permit adequate heart rate response to exercise
- •significant uncorrected primary vascular disease
- •isolated pulmonary hypertension
- •poorly controlled symptomatic postural hypotension
- •obstructive cardiomyopathies
- •Severe untreated anemia.
- •Participation in another research study in the last month
排除标准
- 未提供
结局指标
主要结局
Functional status as measured by handgrip strength.
时间窗: After 12-weeks
Subjects randomized to the intervention group will receive a 12-week Lifestyle Change program intervention
Functional status as measured by the 6-minute walk test.
时间窗: After 12-weeks
Subjects randomized to the intervention group will receive a 12-week Lifestyle Change program intervention
Functional status as measured by New York Heart Association class categories.
时间窗: After 12-weeks
Subjects randomized to the intervention group will receive a 12-week Lifestyle Change program intervention
次要结局
- all-cause mortality(for 1 year after completing the intervention)
- Hospital Admission Rates(During the intervention period of 12 weeks and for 1 year after completing the program.)
研究者
Eva Stuart, RN
Christopher Suhar, MD
Scripps Center for Integrative Medicine