- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01859286
Improving Signout Accuracy and Information Delivery in the Emergency Department (SAID-ED)
17. maj 2013 opdateret af: Justin Mazzillo, The University of Texas Health Science Center, Houston
Improving Transfer of Care Accuracy and Information Delivery in the Emergency Department
The investigators sought to determine if implementing a standardized sign out process would reduce the amount of medical errors related to patient sign out.
The standardized process included the following interventions: implementation of a data resident to review patients lab values, vital signs, radiologist results, and orders in real time, conducting sign out in a standardized location and using the attending physician as an "interruption manager."
The investigators defined medical errors related to sign out as any piece of information was incorrectly reported or omitted during sign out that caused a change in treatment or disposition discussed during sign out.
The investigators hypothesis was that implementing a standardized sign out process would lead to a decrease in the amount of sign out related errors.
Studieoversigt
Status
Afsluttet
Intervention / Behandling
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
321
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Texas
-
Houston, Texas, Forenede Stater, 77030
- Memorial Hermann Hospital - Texas Medical Center
-
-
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
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
ED Physicians.
We looked at the amount of errors due to signout that ED Physicians commit with standard signout procedure and then with a revised signed out process
Beskrivelse
Inclusion Criteria:
- ED transfers of care occurring at 0700 or 1900.
Exclusion Criteria:
- Attending only handovers (1500, 2300)
- Handovers including midlevel providers (Thursday 0700, 1300).
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
regular sign out process
|
The intervention phase included was the introduction of a standardized TOC (transfer of care) process, which occurred during April and May of 2012.
TOC was done at a predefined location in each section of the emergency department (Medicine and Trauma).
All participating residents were given a diagram detailing the central location and seating arrangement.
The outgoing attending was designated to handle all distractions or disturbances that occurred during sign out.
The most senior resident coming on to shift was designated the data resident.
The data resident's role was to operate a centralized computer with the ED tracking board and EMR and review pending orders, vital signs and resulted labs and radiology reports after each patient was signed out.
A brief pause was implemented to allow the oncoming team to ask any questions regarding that patient's care or course.
The post TOC data form and protocol were identical to that of the control phase.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Sign out related errors
Tidsramme: 4 months
|
4 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
perception of sign out
Tidsramme: 1 year after implementation of revised sign out process
|
1 year after implementation of revised sign out process
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Nnaemeka G Okafor, MD, UT Houston Health Sciences Center at Houston Department of Emergency Medicine
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 2012
Primær færdiggørelse (Faktiske)
1. maj 2012
Datoer for studieregistrering
Først indsendt
27. april 2013
Først indsendt, der opfyldte QC-kriterier
17. maj 2013
Først opslået (Skøn)
21. maj 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. maj 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
17. maj 2013
Sidst verificeret
1. maj 2013
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- HSC-MS-11-0655
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 .