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- Klinische proef NCT04035772
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
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.
Studie Overzicht
Gedetailleerde beschrijving
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.
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Quebec
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Lévis, Quebec, Canada, G6V 3Z1
- Pascal Y Smith
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Onderzoek naar gezondheidsdiensten
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: 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. |
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.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Composite performance indicator score (change is assessed)
Tijdsspanne: 30 months prior to implementation and up to 12 months later
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Composite performance indicator score based on 15 process performance indicators found in the Quebec Trauma Registry
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30 months prior to implementation and up to 12 months later
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Rate of complications (change is assessed)
Tijdsspanne: 30 months prior to implementation and up to 12 months later
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Rate of complication in the trauma center
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30 months prior to implementation and up to 12 months later
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Mortality rate (change is assessed)
Tijdsspanne: 30 months prior to implementation and up to 12 months later
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Mortality rate in the trauma center
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30 months prior to implementation and up to 12 months later
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Length of stay (change is assessed)
Tijdsspanne: 30 months prior to implementation and up to 12 months later
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Length of stay in the trauma center
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30 months prior to implementation and up to 12 months later
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Functional Independence Measure (FIM) (change is assessed)
Tijdsspanne: 30 months prior to implementation and up to 12 months later
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an 18-item of physical, psychological and social function
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30 months prior to implementation and up to 12 months later
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Medewerkers en onderzoekers
Sponsor
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Patrick M Archambault, MD MSc FRCPC, CISSS Chaudières-Appalaches (Hôtel-Dieu de Lévis)
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- Wiki Implementation 1415-041
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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Klinische onderzoeken op Trauma
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University Hospital, AngersWerving
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Chang, Steve S., M.D.Santa Barbara Cottage Hospital; Accumetrics, Inc.VoltooidHoofdletsel Trauma BluntVerenigde Staten
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Humacyte, Inc.Actief, niet wervendTrauma | Trauma letsel | Trauma, meerdere | Trauma botOekraïne
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Assistance Publique - Hôpitaux de ParisFrancophone Pediatric Resuscitation and Emergency Group (GFRUP)Voltooid
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Centre Hospitalier Annecy GenevoisBeëindigd
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University Hospital, ToulouseNog niet aan het werven
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Marmara UniversityVoltooid
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Rabin Medical CenterIsraeli Ministry of SecurityOnbekend
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Phoenix Children's HospitalOnbekendVerwaarlozing, kind | Hoofd trauma | Niet-toevallig trauma | Niet-accidenteel letsel aan kind
Klinische onderzoeken op Wiki101 and WikiTrauma
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University of LincolnNottinghamshire Healthcare NHS TrustWerving
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University of HertfordshireVoltooidHartinfarct | Multiple sclerose | Hersenletsel | Ziekte van ParkinsonVerenigd Koninkrijk
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Dalarna UniversityUppsala University; The Swedish Research CouncilWervingDementie | Milde cognitieve stoornis | Dementie, gemengd | Dementie van het Alzheimer-type | Subjectieve cognitieve stoornissen | Dementie SenielZweden
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GlaxoSmithKlineVoltooidTetanus | Difterie | Acellulaire kinkhoestVerenigde Staten
-
University of CalgaryWervingDepressie | Verslaving | Huiselijk geweld | ArmoedeCanada
-
Stanford UniversityNational Institute of Mental Health (NIMH); Washington University School of MedicineVoltooidEet stoornissenVerenigde Staten
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University of Illinois at Urbana-ChampaignOnbekendVal letsel | Valpreventie | Val veiligheid
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USDA Grand Forks Human Nutrition Research CenterCalifornia Polytechnic State University-San Luis ObispoVoltooidInname van groenten en fruit | Voeding voor kinderen | Keuze voor gezonde voeding | Gezonde voedselbereidingVerenigde Staten
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University Hospital MuensterVoltooidTandheelkundige fobieDuitsland
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Fondazione Don Carlo Gnocchi OnlusCatholic University of the Sacred Heart; EMDR EuropeNog niet aan het wervenDepressie | Multiple sclerose