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Clinical Trials/NCT01346462
NCT01346462CompletedNot Applicable

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

University of Pennsylvania1 site in 1 country513 target enrollmentStarted: May 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
513
Locations
1
Primary Endpoint
Completion of Follow-up Appointment with PCP

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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

Exclusion Criteria

  • •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.

Arms & Interventions

PaCT

Experimental

The Patient-Centered Transition Arm

Intervention: 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.

Outcomes

Primary Outcomes

Completion of Follow-up Appointment with PCP

Time Frame: 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.

Secondary Outcomes

  • Morisky Medication Adherence scale.(14 days post-discharge)
  • Patient Activation Measure(14 days post discharge)
  • Self-rated Health(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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shreya Kangovi

Philadelphia Veterans Affairs Medical Center Special Fellow

University of Pennsylvania

Study Sites (1)

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