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临床试验/NCT01346462
NCT01346462已完成不适用

A Randomized Controlled Trial of a Novel Community Health Worker Care Transitions Intervention.

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 513 人开始时间: 2011年5月最近更新:
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
513
试验地点
2
主要终点
Completion of Follow-up Appointment with PCP

研究概览

简要总结

The investigators propose a pilot randomized controlled trial of a care transitions intervention in which trained Community Health Workers will act as supports for socioeconomically vulnerable patients who are being discharged from the Hospital of the University of Pennsylvania and Presbyterian Hospital. CHWs or IMPaCT Partners will help patients to overcome the challenges of transition, including arranging primary care provider (PCP) follow-up, filling medication prescriptions and obtaining referrals to community-based social services. As our primary outcome, the investigators will examine the effect of the IMPaCT intervention on rates of primary care follow-up. The investigators will also examine the effect of IMPaCT on secondary outcome variables including patients' satisfaction with the experience of transition, quality of discharge communication, medication adherence, self- rated health, and inpatient readmission within 30 days after discharge.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participant admitted to the General Medicine services of the Hospital of the University of Pennsylvania (HUP), or Presbyterian Hospital during the enrollment period
  • Participant uninsured or insured by Medicaid at the time of discharge from the hospital
  • Participant is 18-65 years old
  • Participant is willing to participate and be contacted at 14 days post-discharge by telephone or through a home visit by research personnel (if no functioning telephone is present in the household)
  • Participant resides in one of the following zip codes: 19104, 19131, 19139, 19143,
  • These zip codes have the highest frequency of readmissions to HUP and Presbyterian Hospital
  • Participant is English speaking

排除标准

  • Patients with insurance other than Medicaid will be excluded as they are outside of the population of interest for this intervention targeted specifically at socioeconomically vulnerable patients. Dual eligible patients (Medicaid and Medicare) will be excluded. Patients older than 65 are eligible for the Transitional Care Model Intervention, which is a separate intervention offered at Penn Medicine hospitals.
  • Non-English speaking participants will be excluded because in this pilot study, the study only has English-speaking PaCT personnel. In future studies, it will be important to study the effect of PaCT in non-English speaking populations.
  • Patients outside of the target zipcodes are being excluded for feasibility reasons during this pilot study: with only two PaCT Partners, we are choosing to focus our resources on a geographic area that has the highest rates of readmissions in order to facilitate home visits.

研究组 & 干预措施

PaCT

Experimental

The Patient-Centered Transition Arm

干预措施: Patient-Centered Transition Intervention (Behavioral)

Control

No Intervention

Control group patients will receive routine care from the admitting hospital, including routine patient management, and discharge planning.

结局指标

主要结局

Completion of Follow-up Appointment with PCP

时间窗: 14 days post discharge

We hypothesize that compared to patients who receive usual discharge planning, PaCT patients will have a higher proportion of follow-up to PCP within two weeks post-discharge, compared with usual discharge planning.

次要结局

  • Morisky Medication Adherence scale.(14 days post-discharge)
  • Self-rated Health(14 days post-discharge)
  • Patient Activation Measure(14 days post discharge)
  • Patient Satisfaction Questionnaire(14 days post discharge)
  • Acute Care Reutilization(30 days post-discharge)
  • Quality of Discharge Planning(14 days post-discharge)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shreya Kangovi

Philadelphia Veterans Affairs Medical Center Special Fellow

University of Pennsylvania

研究点 (2)

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