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Comparing Remote Interpreter Modalities in the Pediatric Emergency Department

18. maj 2015 opdateret af: K. Casey Lion, Seattle Children's Hospital

Impact of Remote Interpreter Modality on Comprehension, Communication Quality, and Consistency of Interpreter Use in the Pediatric Emergency Department

Professional interpretation improves quality of care for patients with limited English proficiency (LEP). However, many health care settings lack access to professional interpreters, and even in locations with good access, logistical factors and perceived barriers have limited their widespread use. Remote methods of professional interpretation, including telephone and video, hold great promise for expanding access, but only limited data exist on the relative impacts of these modalities on patient care and provider uptake. Comparing how these modalities impact multiple aspects of health care quality, including family comprehension, provider communication, and consistency of provider interpreter use will inform dissemination of strategies for delivery of safe, efficient, and equitable care to LEP families.

Aim 1: To determine whether randomly assigned remote interpreter modality (telephone versus video) impacts parent-reported quality of communication and interpretation, diagnosis comprehension, and length of stay (LOS) among LEP Spanish-speaking families seen in a pediatric Emergency Department (ED).

Hypothesis 1: Parent-reported quality of communication and interpretation and parent diagnosis comprehension will be higher among families assigned to video interpretation compared to telephone interpretation.

Hypothesis 2: LOS will not differ between families assigned to video and telephone interpretation.

Aim 2: To determine whether assigned interpreter modality is associated with provider decision to communicate without professional interpretation.

Hypothesis 3: Parent-reported provider communication without professional interpretation (e.g. using the patient or a family member to interpret for some part of the visit) will be lower for families assigned to video interpretation compared to telephone interpretation.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

208

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Washington
      • Seattle, Washington, Forenede Stater, 98105
        • Seattle Children's Hospital Emergency Department

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

1 dag til 18 år (Barn, Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Preferred language for medical care of Spanish
  • At least one primary caregiver requires interpretation
  • Presenting to Seattle Children's ED during recruiting hours

Exclusion Criteria:

  • Triage level 1 (life-threatening illness)
  • No parent or legal guardian present
  • Reason for visit is concern for abuse
  • reason for visit is primary behavioral or psychiatric complaint

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Telephone Interpretation
These families will be assigned to use telephone interpretation throughout the ED visit.
Professional interpretation provided over the phone by a national network of certified medical interpreters
Eksperimentel: Video Interpretation
These families will be assigned to use video interpretation throughout the ED visit.
Professional interpretation provided over video by a national network of certified medical interpreters

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Communication Quality
Tidsramme: Once, 1-7 days after the ED visit
We will use the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Child Visit Survey 2.0 communication composite, which includes 5 items.
Once, 1-7 days after the ED visit
Interpretation Quality
Tidsramme: Once, 1-7 days after ED visit
Interpretation quality will be measured with the Interpreter Satisfaction Survey (7 items).
Once, 1-7 days after ED visit
Diagnosis Comprehension
Tidsramme: Once, 1-7 days after ED visit
Parents will be asked to name their child's diagnosis. Clinician-recorded diagnosis will be obtained from chart review for comparison. Responses will be classified as correct, incorrect, or vague/incomplete, using a method we have employed previously.
Once, 1-7 days after ED visit
Consistency of Interpreter Use
Tidsramme: Once, 1-7 days after ED visit
Parents will be asked to report on the frequency with which providers used each of a list of potential communication methods (e.g. telephone interpreter, family or friend, spoke in English without an interpreter present). Response options are never, sometimes, frequently, or always.
Once, 1-7 days after ED visit

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Length of ED stay
Tidsramme: Once, after ED visit
Time from arrival in Emergency Department to discharge home or admission to the hospital.
Once, after ED visit

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: K. Casey Lion, MD, MPH, Seattle Children's Hospital

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

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. august 2014

Datoer for studieregistrering

Først indsendt

11. november 2013

Først indsendt, der opfyldte QC-kriterier

15. november 2013

Først opslået (Skøn)

18. november 2013

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

20. maj 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

18. maj 2015

Sidst verificeret

1. maj 2015

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 14647

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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