Study Stopped
Feasibility (barriers to implantation within the institution)
The WikiTrauma Interrupted Time Series Protocol
WikiTrauma
Implementation and Evaluation of a Wiki Involving Multiple Stakeholders Including Patients in the Promotion of Best Practices in Trauma Care: the WikiTrauma Interrupted Time Series Protocol
1 other identifier
interventional
6
1 country
1
Brief Summary
The purpose of this study is to study the combined effect of WikiTrauma, a free collaborative database of clinical decision support tools, and Wiki101, a training course teaching participants how to use WikiTrauma, on the quality of care in four trauma centers in Quebec. The hypothesis that the theory-based intervention (Wiki101), in combination with use of WikiTrauma, will result in better adoption of best practices in trauma care, safer care (less complications), improved patient outcomes and less costly care in Canada.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2016
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2016
CompletedFirst Submitted
Initial submission to the registry
January 18, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2018
CompletedFirst Posted
Study publicly available on registry
July 29, 2019
CompletedJuly 29, 2019
July 1, 2019
2.4 years
January 18, 2018
July 26, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Composite performance indicator score (change is assessed)
Composite performance indicator score based on 15 process performance indicators found in the Quebec Trauma Registry
30 months prior to implementation and up to 12 months later
Secondary Outcomes (4)
Rate of complications (change is assessed)
30 months prior to implementation and up to 12 months later
Mortality rate (change is assessed)
30 months prior to implementation and up to 12 months later
Length of stay (change is assessed)
30 months prior to implementation and up to 12 months later
Functional Independence Measure (FIM) (change is assessed)
30 months prior to implementation and up to 12 months later
Study Arms (1)
Wiki101 and WikiTrauma
EXPERIMENTALWiki101, a theory-based continuing professional development (CPD) program, will train participants at the selected trauma centers to use WikiTrauma effectively and safely to create and share different types of Knowledge Transfer (KT) tools (e.g., care protocols, order sets, patient decision aids). Participants will receive Wiki101 training and then gain access to WikiTrauma with editing rights to the knowledge implementation tools (e.g. care protocols, order sets, care pathways) found in the wiki. WikiTrauma is the wiki we created to promote best practices in trauma care and will be implemented in four trauma centers in Quebec during 12 months. During this period, we will continue to measure the impact on the quality of care.
Interventions
Wiki101 is a theory-based continuing professional development course to teach healthcare professionals how to use WikiTrauma. WikiTrauma is a wiki containing implementation tools built upon the Google Sites platform.
Eligibility Criteria
You may qualify if:
- decision makers (eg, trauma program coordinators) or,
- health care professionals (eg, emergency physicians, critical care physicians, trauma surgeons, nurses, respiratory therapists, physiotherapists, or pharmacists).
- Patient representatives will be selected without any restrictions or limitations with regard to the qualifications.
- Health care professional students and trainees (eg, residents, medical students, and nursing students) will have the same access to WikiTrauma and Wiki101 as fully certified professionals.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Laval Universitylead
- Canadian Medical Protective Associationcollaborator
Study Sites (1)
Pascal Y Smith
Lévis, Quebec, G6V 3Z1, Canada
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Patrick M Archambault, MD MSc FRCPC
CISSS Chaudières-Appalaches (Hôtel-Dieu de Lévis)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
January 18, 2018
First Posted
July 29, 2019
Study Start
May 1, 2016
Primary Completion
October 1, 2018
Study Completion
December 20, 2018
Last Updated
July 29, 2019
Record last verified: 2019-07