CClinicalTrials.gg
TerminatedNCT04035772WikiTraumaUpdated Jul 29, 2019

The WikiTrauma Interrupted Time Series Protocol

An interventional study of Wiki101 and WikiTrauma in Trauma, sponsored by Laval University. Terminated at 1 site in Canada. Per ClinicalTrials.gov, last updated 2019-07-29.

Sponsored by Laval University · Not applicable, Interventional, and Health services research

Why this study was terminated
Feasibility (barriers to implantation within the institution)

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled May 2016, registered Jan 2018).
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Not applicable
Sex
All
01

Study 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.

Read the detailed description

Trauma is the most common cause of mortality among people between the ages of 1 and 45 years, costing Canadians 19.8 billion dollars a year (2004 data), yet half of all patients with major traumatic injuries do not receive evidence-based care, and significant regional variation in the quality of care across Canada exists. Accordingly, the goal of this study is to lead a research project in which stakeholders themselves will adapt evidence-based trauma care knowledge tools to the varied institutional contexts and cultures. This will be done by developing and assessing the combined impact of WikiTrauma, a free collaborative database of clinical decision support tools, and Wiki101, a training course teaching participants how to use WikiTrauma. WikiTrauma has the potential to ensure that all stakeholders (eg, patients, clinicians, and decision makers) can all contribute to, and benefit from, evidence-based clinical knowledge about trauma care that is tailored to the needs and clinical setting.

The main goal will be to study the combined effect of WikiTrauma and Wiki101 on the quality of care in four trauma centers in Quebec.

First, the wiki will be pilot-tested with potential users to create a version ready to test in practice. A rapid, iterative prototyping process with 15 health professionals from nonparticipating centers will allow to identify and resolve usability issues prior to finalizing the definitive version for the interrupted time series. Second, an interrupted time series will be performed to measure the impact of the combined intervention on the quality of care in four trauma centers that will be selected;one level I, one level II, and two level III centers. Participants will be health care professionals working in the selected trauma centers. Also, five patient representatives will be recruited to participate in the creation of knowledge tools destined for the use (eg, handouts). All participants will be invited to complete the Wiki101 training and then use, and contribute to, WikiTrauma for 12 months. The primary outcome will be the change over time of a validated, composite, performance indicator score based on 15 process performance indicators found in the Quebec Trauma Registry.

The project was funded in November 2014 by the Canadian Medical Protective Association. The trial will start in early 2015 and preliminary results should be available in June 2016. Two trauma centers have already agreed to participate and two more will be recruited in the next months.

This study is expected to add important and unique evidence about the effectiveness, safety, and cost savings of using collaborative platforms to adapt knowledge implementation tools across jurisdictions.

02

Conditions studied

  • Trauma

Browse trials for

Keywords

  • interrupted time series
  • wiki
  • quality improvement
  • knowledge translation
  • trauma care
  • stakeholder engagement
  • adaptating knowledge tools
03

In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's enrollment of 6 is below the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Laval University is the lead sponsor of 371 studies on the registry; 68 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
6 participants (actual)

Study arms

  • Experimental
    Wiki101 and WikiTrauma

    Wiki101, 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.

    Other: Wiki101 and WikiTrauma

Interventions

  • OtherWiki101 and WikiTrauma

    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.

06

What researchers measure

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

    Time frame: 30 months prior to implementation and up to 12 months later

Secondary outcomes

  1. Rate of complications (change is assessed)

    Rate of complication in the trauma center

    Time frame: 30 months prior to implementation and up to 12 months later

  2. Mortality rate (change is assessed)

    Mortality rate in the trauma center

    Time frame: 30 months prior to implementation and up to 12 months later

  3. Length of stay (change is assessed)

    Length of stay in the trauma center

    Time frame: 30 months prior to implementation and up to 12 months later

  4. Functional Independence Measure (FIM) (change is assessed)

    an 18-item of physical, psychological and social function

    Time frame: 30 months prior to implementation and up to 12 months later

07

Study locations

1 site
  • Pascal Y Smith
    Lévis, Quebec G6V 3Z1, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04035772
Lead sponsor
Laval University
Collaborators
Canadian Medical Protective Association
Responsible party
Patrick Archambault (Associate Professor, Laval University) — Principal investigator
First posted
Jul 29, 2019
Start date
May 2016
Primary completion
Oct 2018
Completion
Dec 20, 2018
Last update
Jul 29, 2019

Study contacts

Patrick M Archambault, MD MSc FRCPC
principal investigator · CISSS Chaudières-Appalaches (Hôtel-Dieu de Lévis)

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jul 2019. 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