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Clinical Trials/NCT02388711
NCT02388711
Completed
N/A

A Randomized Control Trial of the Coordinated-Transitional Care (C-TraC) Intervention for Dementia Patients

University of Wisconsin, Madison1 site in 1 country584 target enrollmentMarch 2015
ConditionsDementia

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dementia
Sponsor
University of Wisconsin, Madison
Enrollment
584
Locations
1
Primary Endpoint
Change from baseline in rehospitalizations at 14, 30 and 90-days
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The goal of the project is to conduct a prospective, randomized-controlled clinical trial to determine the extent to which the Coordinated-Transitional Care (C-TraC) program impacts transitional care quality, patient cognition/function, caregiver stress and 30-day rehospitalizations in patients with documented diagnoses of dementia discharged from the hospital to the community.

Detailed Description

Patients with dementia often experience poor quality transitions from the hospital to the community. In response, the investigators developed and piloted the Coordinated-Transitional Care (C-TraC) program--a low-cost, telephone-based intervention designed to improve care coordination and outcomes in hospitalized patients with dementia or other high-risk conditions discharged to community settings. A single-blind, prospective, randomized-controlled trial will be used with participants being randomly assigned to receive usual (i.e. standard) care, or usual care plus the C-TraC intervention. Outcomes will be assessed via scheduled phone-calls at 14, 30, and 90 days post-hospitalization. A 45-day phone call will also be conducted to complete a brief satisfaction survey with the caregiver about their post-hospital experience.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
October 11, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • English-speaking
  • Have a working telephone
  • Hospitalized on medical inpatient wards at UWHC
  • A documented pre-hospitalization diagnosis of dementia.
  • Alzheimer's Disease Cooperative Study - Clinical Dementia Rating (ADCS-CDR) score of \> 0
  • Have a family member/informal caregiver who has regular contact with them in the community setting
  • Caregiver Inclusion Criteria:
  • English-speaking
  • Have a working telephone
  • Have contact with patient a minimum of once per week

Exclusion Criteria

  • Discharged to institutional settings
  • No identified caregiver
  • Discharged to hospice
  • Followed by complex case management or any form of intensive case management (e.g. transplant, congestive heart failure, dialysis)
  • Score moderate-high on modified ASSIST tool for alcohol

Outcomes

Primary Outcomes

Change from baseline in rehospitalizations at 14, 30 and 90-days

Time Frame: 14, 30 and 90-days

The presence of any rehospitalization will be assessed through a combination of 14, 30 and 90 day structured phone calls directly to patients/caregivers, a detailed review of medical records associated with any of these caregiver/patient reported rehospitalizations, and a detailed review of the patient's UWHC medical records after all phone calls are completed.

Secondary Outcomes

  • Patient functional maintenance/recovery(14, 30 and 90-days)
  • Increase in patient delirium prevention/resolution(14, 30 and 90-days)
  • Patient falls prevention(14, 30 and 90-days)
  • Decrease caregiver stress(14, 30 and 90-days)

Study Sites (1)

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