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Testing the Re-Engineered Hospital Discharge

This study has been completed.
Information provided by (Responsible Party):
Brian Jack, Boston University Identifier:
First received: November 10, 2005
Last updated: February 27, 2017
Last verified: February 2017
Results First Received: February 10, 2009  
Study Type: Interventional
Study Design: Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Single (Outcomes Assessor);   Primary Purpose: Prevention
Condition: All
Intervention: Behavioral: Re-Engineered Hospital Discharge

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
All participants were recruited between January 1, 2006 and October 16, 2007, from the general medical floors at Boston Medical Center.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
The baseline interview was conducted after enrollment and prior to group assignment, but it did not affect this assignment or lead to exclusion from the study for any participant. All participants who gave consent and agreed to be in the study were assigned to a group

Reporting Groups
Re-engineered Hospital Discharge Participants received the "Re-Engineered Hospital Discharge", a set of 11 discrete, mutually reinforcing components provided by a Discharge Advocate and re-enforced by a telephone call 2-4 days after discharge by a clinical pharmacist.
Standard Hospital Discharge Participants received the routine, standard hospital discharge.

Participant Flow:   Overall Study
    Re-engineered Hospital Discharge   Standard Hospital Discharge
STARTED   373   376 
COMPLETED   370   368 
Withdrawal by Subject                2                5 
Death                1                2 
Participant previously enrolled                0                1 

  Baseline Characteristics

  Outcome Measures

1.  Primary:   Total Number of Rehospitalizations (Emergency Department Visits Plus Hospital Admissions) in the 30 Days After Discharge.   [ Time Frame: 30 days after discharge ]

  Serious Adverse Events

  Other Adverse Events

  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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