A Virtual Ward to Reduce Readmissions After Hospital Discharge
1 other identifier
interventional
1,928
1 country
5
Brief Summary
The purpose of this study is to see whether a Virtual Ward reduces readmissions after hospital discharge.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2010
Longer than P75 for not_applicable
5 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 13, 2010
CompletedFirst Posted
Study publicly available on registry
April 21, 2010
CompletedStudy Start
First participant enrolled
June 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2014
CompletedDecember 9, 2013
December 1, 2013
3 years
April 13, 2010
December 6, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
Composite of readmission to hospital or death.
A binary outcome variable for each patient, representing either readmission to hospital or death within 30 days of hospital discharge. A research assistant blinded to the assignment will ascertain this information via telephone using a standardized script. Second, we may also ascertain this information by linking the data we collect to administrative databases housed at the Institute for Clinical Evaluative Sciences.
30 days after hospital discharge
Secondary Outcomes (20)
Composite of readmission or death
90 days after discharge
Composite of readmission or death
6 months after discharge
Composite of readmission or death
One year after discharge
Emergency department visits
30 days after discharge
Emergency department visits
90 days after discharge
- +15 more secondary outcomes
Study Arms (2)
Usual Care
ACTIVE COMPARATORVirtual Ward
EXPERIMENTALInterventions
A multidisciplinary team to optimize medical and social care for patients residing in their own homes
Eligibility Criteria
You may qualify if:
- Discharge from medical service
- LACE score greater than or equal to 10
- Age greater than or equal or 18
- Resident in Toronto Central Local Health Integration Network catchment area
- Patient or designate able to speak English well enough for follow up telephone calls
You may not qualify if:
- Previously enrolled in study
- Discharged to a rehabilitation or complex continuing care facility
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Unity Health Torontolead
- Canadian Institutes of Health Research (CIHR)collaborator
- Toronto Central Local Health Integration Networkcollaborator
- Ontario Ministry of Health and Long Term Carecollaborator
- Toronto Central Community Care Access Centrecollaborator
- Women's College Hospitalcollaborator
- University Health Network, Torontocollaborator
- Sunnybrook Health Sciences Centrecollaborator
Study Sites (5)
St. Michael's Hospital
Toronto, Ontario, M5B 1W8, Canada
Sunnybrook Health Sciences Centre
Toronto, Ontario, Canada
Toronto Central Community Care Access Centre
Toronto, Ontario, Canada
University Health Network
Toronto, Ontario, Canada
Women's College Hospital
Toronto, Ontario, Canada
Related Publications (2)
van Walraven C, Dhalla IA, Bell C, Etchells E, Stiell IG, Zarnke K, Austin PC, Forster AJ. Derivation and validation of an index to predict early death or unplanned readmission after discharge from hospital to the community. CMAJ. 2010 Apr 6;182(6):551-7. doi: 10.1503/cmaj.091117. Epub 2010 Mar 1.
PMID: 20194559BACKGROUNDDhalla IA, O'Brien T, Morra D, Thorpe KE, Wong BM, Mehta R, Frost DW, Abrams H, Ko F, Van Rooyen P, Bell CM, Gruneir A, Lewis GH, Daub S, Anderson GM, Hawker GA, Rochon PA, Laupacis A. Effect of a postdischarge virtual ward on readmission or death for high-risk patients: a randomized clinical trial. JAMA. 2014 Oct 1;312(13):1305-12. doi: 10.1001/jama.2014.11492.
PMID: 25268437DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Irfan Dhalla, MD, MSc
St. Michael's Hospital/University of Toronto
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Staff Physician & Scientist
Study Record Dates
First Submitted
April 13, 2010
First Posted
April 21, 2010
Study Start
June 1, 2010
Primary Completion
June 1, 2013
Study Completion
June 1, 2014
Last Updated
December 9, 2013
Record last verified: 2013-12