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临床试验/NCT02045147
NCT02045147已完成不适用

Home Based Care Transitions Tailored by Cognition and Patient Activation: A Prudent Use of Transitional Care Resources

University of Nebraska1 个研究点 分布在 1 个国家目标入组 263 人开始时间: 2013年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
263
试验地点
1
主要终点
Health Care Utilization

研究概览

简要总结

There is overwhelming evidence that patients with multiple chronic illnesses need better self-management skills. Discharge from the hospital may not be the most opportune time to be teaching patients these self-management skills. There are several different care transition models being used across the country; however we know that not every patient needs the same type or amount of an intervention. The purpose of this pilot study is to study the impact delivering a home based care transitions intervention (HBCTI) with four different groups tailored on cognition and level of patient activation compared to usual care (UC) resulting in 8 study arms on the outcomes of health care utilization (HCU) and health outcomes: patient-reported health status, assessment of care for chronic conditions, and health related quality of life in adult patients with multiple chronic diseases dismissed to home from an acute care facility. Our working hypothesis is that patients in the HBCTI groups compared to the UC groups will have lower HCU and improved outcomes (patient-reported health status, assessment of care for chronic conditions, and health related quality of life).

详细描述

One in five Medicare patients discharged from the hospital experience readmission within 30 days. Too often, hospital readmissions result from inadequate transition from hospital to home at discharge. Care transitions are complicated because of high patient acuity, multiple comorbidities, decreased length of stay, and multiple clinician involvement increasing the number of handoffs. With decreased length of stay, many patients do not comprehend or feel confident with instructions for discharge, thus management of their chronic illnesses are difficult. Most formal care transition programs are standardized and every patient receives similar strategies or interventions. However, it has been well documented that patients with cognitive problems and decreased activation are at high risk for re-hospitalization related to impaired self-management. We believe that assessment of cognition and patient activation during the patient's hospitalization will provide valuable information for discharge interventions. Data related to cognition and activation can be used to tailor discharge planning and help determine what type and how many resources are needed for individual patients after hospital discharge. The purpose of this feasibility study is to examine the impact of delivering a home based care transitions interventions (HBCTIs) with four different groups tailored on cognition and level of patient activation compared to usual care (UC) on the outcomes of health care utilization (HCU) and health outcomes: patient-reported health status, assessment of care for chronic conditions, and health related quality of life in adult patients with multiple chronic diseases discharged to home from the hospital.

We will test our intervention with the following aims: Aim 1.To evaluate the impact of HBCTIs on health care utilization. We will measure HCU (number of emergency department(ED) visits and number of readmissions) at 6 months after discharge. Our working hypothesis is that patients in the HBCTI groups compared to the UC groups will have lower HCU over time (6 months); Aim 2. To evaluate the impact of HBCTIs on the following health outcomes: patient-reported health status (PROMIS-29), assessment of care for chronic conditions (PACIC), and quality of life (EuroQol). Our working hypothesis is that patients in the HBCTI groups compared to the UC group will have improved patient-reported health status, assessment of care for chronic conditions, and quality of life (EuroQol) at 6 months after discharge.

The findings from this study have the potential to change this paradigm in three ways: 1) we will gain a better understanding of the role of cognition and patient activation in promoting self-management to enhance outcomes; 2). our innovative approach, which considers the unique needs of patients based on their level of cognition and patient activation will advance new concepts in care transition programs; 3) we will have a better understanding of varying intensities of visits, level of providers, and type and amount of strategies administered. This practical model for care transitions could serve as a model within the larger health care delivery system that could result in significant cost savings.

研究设计

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

入排标准

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

入选标准

  • •Adult Patients (age 19 and older) being discharged from the hospital with three or more chronic diseases;
  • •Have a score greater than 17 on the Montreal Cognitive Assessment (dementia);
  • •Reside within a 35 mile radius of Lincoln, Ne.; and
  • •Able to hear, speak and read English.

排除标准

  • •Patients will be excluded if they:
  • •have a terminal illness;
  • •have a score of less than 17 on the Montreal Cognitive Assessment (dementia);
  • •are under the care of The Physicians Network (TPN) at St. Elizabeth Regional Medical Center (SERMC).

研究组 & 干预措施

Grp 1a: Low Cognition, Low Activation

Experimental

Subjects will receive an 8 week care transition intervention with an Advanced Practice Registered Nurse-Nurse Practitioner (APRN-NP) and Certified Nursing Assistant (CNA). The APRN-NP will guide the care transition intervention. This group will receive the most intense intervention.

干预措施: Grp 1a Low Cognition, Low Activation Intervention (Behavioral)

Grp 2a: Low Cognition, High Activation

Experimental

Subjects will receive an 8 week care transition intervention with an APRN-NP and CNA. The APRN-NP will guide the care transition intervention. This group will receive an intense intervention.

干预措施: Grp 2a Low Cognition, High Activation Intervention (Behavioral)

Grp 3a: Normal Cognition, Low Activation

Experimental

Subjects will receive an 4 week care transition intervention with a Registered Nurse (RN) Coach. This group will be evaluated at four weeks, if the patient activation levels are still low, they will be referred to the 4 week APRN-NP and CNA.

干预措施: Grp 3a Normal Cognition, Low Activation Intervention (Behavioral)

Grp 4a: Normal Cognition, High Activation

Experimental

Subjects will receive the least intensive intervention delivered by a RN coach.

干预措施: Grp 4a Normal Cognition, High Activation Intervention (Behavioral)

Grp 1b: Low Cognition, Low Activation Usual Care

No Intervention

Comparison group to 1a intervention group

Grp 2b Low Cognition, High Activation Usual Care

No Intervention

Comparison group to 2a intervention group

Grp 3b: Normal Cognition, Low Activation Usual Care

No Intervention

Comparison group to 3a intervention group

Grp 4b: Normal Cognition, High Activation Usual Care

No Intervention

Comparison group to 4a intervention group

结局指标

主要结局

Health Care Utilization

时间窗: 6 months

Patient report of number of Emergency Department Visits and number of re-admissions to the hospital within a 6 month time period was measured. Validation data was obtained from the clinical sites.

次要结局

  • EQ-5D Visual Analog Scale (VAS)(6 months)
  • Patient-Reported Outcomes Measurement Information System - Pain Interference(6 months)
  • Patient-Reported Outcomes Measurement Information System-Physical Functioning(6 months after intervention)
  • Patient-Reported Outcomes Measurement Information System-Satisfaction With Social Roles(6 months)
  • Patient-Reported Outcomes Measurement Information System- Anxiety(6 months)
  • Patient-Reported Outcomes Measurement Information System-Fatigue(6 months)
  • Patient-Reported Outcomes Measurement Information System- Depression(6 months)
  • Patient-Reported Outcomes Measurement Information System-Sleep Deprivation(6 months)
  • Patient Assessment of Chronic Illness Care(6 months)
  • Health Related Quality of Life EuroQol-5D (EQ-5D)(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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