CClinicalTrials.gg
CompletedNCT00550264Updated Jun 28, 2011

Study of Physician Awareness of and Communication About Patient Readmissions to the Hospital

An interventional study of Automatic notification of readmissions in Hospital Readmission, sponsored by Brigham and Women's Hospital. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2011-06-28.

Sponsored by Brigham and Women's Hospital · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
500
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Patients admitted to inpatient medicine services often require early hospital readmission, and often they are readmitted to different physician or team, potentially without the knowledge of the prior physician or team. Thus, physicians may lose the opportunity to share valuable information about readmitted patients, which may be detrimental to continuity of care and patient safety. The purpose of this study is to determine baseline awareness and communication rates among physicians regarding readmissions, and then measure the effect of automatic notification on these rates.

02

Conditions studied

  • Hospital Readmission

Keywords

  • Hospital Readmission
  • Continuity of Care
  • Quality of Health Care
03

In context

Lead sponsor

Brigham and Women's Hospital is the lead sponsor of 1,236 studies on the registry; 224 are open to participants now.

Of its 116 completed or terminated interventional studies of FDA-regulated products, 64 (55%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • All patients admitted to the general medicine service at two academic medical centers, and unexpectedly readmitted within 14 days.

Exclusion criteria

Exclusion Criteria:

  • Patients readmitted to the same physician(s), or those whose readmission was planned
05

Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
500 participants (estimated)

Study arms

  • Experimental
    1

    Other: Automatic notification of readmissions

  • No intervention
    2

Interventions

  • OtherAutomatic notification of readmissions

    The experimental group physicians will receive automatic e-mail notification when a patient is readmitted, including contact information for the readmitting team.

06

What researchers measure

Primary outcomes

  1. Physician Awareness and Communication Rates

    Time frame: Within 24 hours of readmission time

07

Study locations

1 site
  • Brigham & Women's Hospital
    Boston, Massachusetts 02115, United States
08

References and documents

Publications

  • Roy CL, Kachalia A, Woolf S, Burdick E, Karson A, Gandhi TK. Hospital readmissions: physician awareness and communication practices. J Gen Intern Med. 2009 Mar;24(3):374-80. doi: 10.1007/s11606-008-0848-x. Epub 2008 Nov 4. PubMed 18982395 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 28, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00550264
Lead sponsor
Brigham and Women's Hospital
Collaborators
Harvard Risk Management Foundation
First posted
Oct 29, 2007
Start date
Feb 2007
Primary completion
Jan 2008
Completion
Jan 2008
Last update
Jun 28, 2011

Study contacts

Christopher L Roy, MD
principal investigator · Brigham and Women's Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2011. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion