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临床试验/NCT05562037
NCT05562037已完成不适用

Stepped Care vs Center-based Cardiopulmonary Rehabilitation for Older Frail Adults Living in Rural MA

Peter Lindenauer, MD4 个研究点 分布在 1 个国家目标入组 139 人开始时间: 2022年9月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
139
试验地点
4
主要终点
Adherence

研究概览

简要总结

This feasibility trial will focus on older adults 60+ who are candidates for cardiac or pulmonary rehabilitation and who are vulnerable, mildly or moderately frail. The investigators will randomize older frail adults living in rural regions of the county to Treatment as usual (TAU) or Stepped care (SC). TAU refers to center-based rehabilitation (CBR). Patients randomized to SC will be enrolled in traditional CBR and based on prespecified non-response criteria, will step up to three services: 1) Transportation-subsidized CBR, 2) Home-based telerehabilitation (TR), and 3) Community health worker-(CHW) supported home-based TR.

详细描述

Cardiac rehabilitation (CR) decreases mortality and both CR and pulmonary rehabilitation (PR) improve function, quality of life, and decrease readmission rates. Despite their proven efficacy, both programs are grossly underutilized, with fewer than 20% of eligible persons participating. Patients with heart and lung disease living in rural communities have even lower rates of participation.

The objective of this proposal is to test the feasibility of performing a full-scale randomized controlled trial (RCT) to compare the effectiveness and value of a stepped care (SC) model versus treatment as usual (TAU) in older frail adults living rural counties. TAU refers to center-based rehabilitation (CBR). The SC model includes initial enrollment into CBR followed by possible step up to three interventions based on prespecified non-response criteria: 1) Transportation-subsidized CBR, 2) Home-based telerehabilitation (TR), and 3) Community health worker-(CHW) supported home-based TR. Unlike traditional SC models, the initial treatment in this model, i.e. CBR, is not the least resource intensive. CBR was chosen as the initial option because it is currently considered the standard of care.

The investigators will conduct a parallel, 2-arm, randomized controlled feasibility trial. Eligible participants will be randomized to TAU (CBR) or SC. Because of the urgent need to address underuse of both CR and PR in rural regions, the proposed feasibility trial will enroll patients referred to either CR or PR. Both arms include an in-person intake evaluation conducted by a certified rehabilitation nurse in the rehabilitation center to determine exercise tolerance and design a tailored 8-week rehabilitation program. Patients randomized to TAU participate in two weekly sessions at the center and are encouraged to exercise at home in between sessions. Patients randomized to the SC arm will also be enrolled in the CBR program. Those who meet prespecified non-response criteria will be stepped up to transportation-subsidized CBR. Providing transportation may not be sufficient for frail older adults who are reluctant to leave their homes in the winter, unfamiliar with exercising, or do not want to exercise in a group setting. Thus, non-responders, will be stepped up to home-based TR. Home-based rehabilitation will be supported by Chanl Health, a virtual platform that supports education and self-management, remote monitoring, and coaching by rehabilitation specialists. Non-responders will be stepped up to CHW-supported home-based TR. The CHW will be help participants use the mobile app, access educational materials, clarify educational content, and exercise during biweekly in-person visits.

Purpose: Heart and lung disease are the first and third leading causes of mortality in the US, respectively. Cardiac rehabilitation (CR) decreases mortality and both CR and pulmonary rehabilitation (PR) improve function, quality of life, and decrease readmission rates. Despite their proven efficacy, both programs are grossly underutilized, with fewer than 20% of eligible persons participating. Patients living in rural communities have even lower rates of participation. Home-based CR and PR has been developed with the goal of improving uptake, and low to moderate strength evidence indicates that these programs are as effective as center-based programs. Further work is needed, however, to examine how best to increase utilization of CR and PR in rural communities. While several studies have examined approaches to improve referral and enrollment, there is little evidence on how to optimize adherence to CR, and no evidence how to optimize adherence to PR.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

盲法说明

Outcome measures will be obtained by a blinded research assistant over the phone within 1 week of completing the 8 week rehabilitation program

入排标准

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

入选标准

  • Older adults (greater than 60 years of age)
  • Live in a Level 1 or 2 state designated rural area in Berkshire County
  • Has a condition qualifying for reimbursement (by government or private insurance) for cardiac or pulmonary rehabilitation
  • Score of 4, 5 or 6 on the Clinical Frailty Scale(24) (corresponding to vulnerable, mildly frail, and moderately frail)

排除标准

  • Attended pulmonary or cardiac rehabilitation within the previous two years
  • Resting pulse oximetry < 85% on room air or while breathing the prescribed level of supplemental oxygen
  • Unstable asthma with hospital admission or ED visit within previous three months
  • Severe exercise-induced hypoxemia, not correctable with oxygen supplementation
  • Acute systemic illness or fever
  • Complex ventricular arrhythmias
  • Resting systolic blood pressure greater than 200mmhg
  • Resting diastolic blood pressure greater than 100mmhg
  • Orthostatic blood pressure (BP) drop of >20 mm Hg with symptoms
  • History of arrhythmia with syncope
  • Severe symptomatic valvular disease
  • Unstable angina
  • Uncontrolled atrial or ventricular arrhythmias
  • Uncontrolled sinus tachycardia (>120 BPM)
  • Uncompensated congestive heart failure
  • Third degree heart block without a pacemaker
  • Active pericarditis or myocarditis
  • Acute cor pulmonale, severe pulmonary hypertension
  • Resting ST displacement > 2mm
  • Uncontrolled diabetes (resting blood glucose >400 mg/dl)
  • Conditions other than pulmonary or cardiac that prohibit exercise (e.g., arthritis, severe neurologic, hepatic or renal disease)
  • Planned surgery or transplantation
  • Hearing impairment limiting ability to participate in data collection by telephone
  • Life expectancy less than one year
  • Significant cognitive deficit and/or psychiatric illness that interferes with ability to provide consent, follow directions, or adhere to study procedures
  • referral to cardiac rehab after coronary artery bypass graph (CABG) and valvular surgery

结局指标

主要结局

Adherence

时间窗: 8 weeks

Proportion of older frail adults randomized to SC attending prescribed rehabilitation sessions

Burden of Data Collection

时间窗: 8 weeks

Baseline Measurement Completion- The investigators need to reach \>80% of baseline data to move forward with this study

Recruitment

时间窗: 3 years

Average number of eligible patients randomized per month

Retention

时间窗: 8 weeks

Proportion in SC arm completing outcome measures

次要结局

  • PROMIS Dyspnea severity(1 week prior to start and 1 week after completion of rehabilitation)
  • PASE(1 week prior to start and 1 week after completion of rehabilitation)
  • Short Physical Performance Battery (SPPB)(1 week prior to start and 1 week after completion of rehabilitation)
  • PROMIS Physical function(1 week prior to start and 1 week after completion of rehabilitation)
  • PROMIS Dyspnea functional limitation(1 week prior to start and 1 week after completion of rehabilitation)
  • Smoking(1 week prior to start and 1 week after completion of rehabilitation)
  • PROMIS Social isolation(1 week prior to start and 1 week after completion of rehabilitation)
  • PROMIS anxiety(1 week prior to start and 1 week after completion of Rehabilitation)
  • EuroQol (EQ-5D-5L)(1 week prior to start and 1 week after completion of rehabilitation)
  • 6 Minute walk test (6-MWT)(1 week prior to start and 1 week after completion of rehabilitation)
  • PROMIS Depression/Sadness(1 week prior to start and 1 week after completion of rehabilitation)

研究者

发起方
Peter Lindenauer, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Peter Lindenauer, MD

Principal Investigator

Baystate Medical Center

研究点 (4)

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