The Educational ARDS Diagnosis Study (READS)
3. september 2014 opdateret af: Eddy Fan, University of Toronto
Randomized Educational ARDS Diagnosis Study (READS)
Without rigorous, high-quality training materials, the results of the LUNG-SAFE study examining the global incidence and outcomes of severe lung failure (acute respiratory distress syndrome [ARDS]) could be confused by either under-recognition of patients with, or misclassification of patients without, ARDS.
This problem has been previously identified with the use of the prior ARDS definitions, particularly in patients with milder severity of illness.
Importantly, the chest x-ray criteria in the ARDS definition has demonstrated only moderate reliability when applied by experts, although this can be improved through the use of training radiographs (as will be used in this educational module).
The investigators hypothesize that the training from the educational module will allow more accurate diagnosis of ARDS by data collectors/study coordinators participating in the LUNG-SAFE study.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
In this LUNG-SAFE sub-study, the investigators will evaluate the effect of a brief online educational module on correctly identifying patients (i.e., standardized cases) with ARDS according to the Berlin Definition.
The investigators hypothesize that the training from the educational module will allow more accurate diagnosis of ARDS according to the Berlin Definition by participating data collectors/study coordinators.
Data collectors and study coordinators from ICUs participating in LUNG-SAFE would be randomized (by simple random number generator) to one of the following online educational streams:
- Educational module completion followed by evaluation
- Evaluation followed by educational module completion
Limited demographic data will be collected from the respondents, along with their responses to the 15 multiple choice test questions. Time spent viewing the educational module will also be collected.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
600
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Ontario
-
Toronto, Ontario, Canada
- SunnyBrook Health Sciences Centre
-
Toronto, Ontario, Canada
- University Health Network
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Study coordinators/data collectors for the LUNG-SAFE study
Exclusion Criteria:
- No informed consent to participate
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Diagnostisk
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Educational Module First
Respondents will complete the online educational module first, followed by the evaluation
|
A descriptive video detailing the diagnosis of ARDS according to the Berlin Definition, along with online educational materials available for review.
|
|
Placebo komparator: Evaluation First
Respondents will complete the the evaluation first, followed by the online educational module
|
The respondents will view the descriptive video detailing the diagnosis of ARDS according to the Berlin Definition, along with online educational materials available for review only after they have completed the evaluation.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
ARDS Diagnosis
Tidsramme: up to 4 weeks
|
The number of correct responses to the evaluation component (15 multiple choice questions) of the educational module (in aggregate).
|
up to 4 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
ARDS Diagnosis
Tidsramme: up to 4 weeks
|
Number of correct responses to the evaluation component of the educational modules, separated by question type (vignettes vs. chest x-rays)
|
up to 4 weeks
|
|
Time
Tidsramme: up to 4 weeks
|
Amount of time spent completing the educational module
|
up to 4 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Eddy Fan, MD, PhD, University Health Network and Mount Sinai Hospital
- Ledende efterforsker: Gordon Rubenfeld, MD, MSc, SunnyBrook Health Sciences Centre
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. februar 2014
Primær færdiggørelse (Faktiske)
1. august 2014
Studieafslutning (Faktiske)
1. september 2014
Datoer for studieregistrering
Først indsendt
31. januar 2014
Først indsendt, der opfyldte QC-kriterier
3. februar 2014
Først opslået (Skøn)
4. februar 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
4. september 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. september 2014
Sidst verificeret
1. september 2014
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- READS1
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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