Optimizing of Waiting - Time in the Anesthesia Admissions Ambulance of the Charité - University Medicine Berlin by Support of a Mobile Application - a Pilot Study
30. juli 2015 opdateret af: Claudia Spies, Charite University, Berlin, Germany
Optimization of Waiting - Time in the Anesthesia Admissions Ambulance Department of Anaesthesia and Intensive Care Medicine CVK/CCM, Charité - University Medicine Berlin by Support of a Mobile Application - a Pilot Study
In this study the investigators measure and optimize the patients waiting time in the preanesthetic assessment by integrating an interactive mobile device.
The aim of this study is to observe whether the patients mean waiting-time is reduced by the use of a special mobile application (Anaest-App) and, as a result , raises patient-satisfaction.
Studieoversigt
Status
Trukket tilbage
Detaljeret beskrivelse
3000 patients as well as medical doctors receive tablet-devices.
The Software (App) installed on these devices coordinates the virtual waiting numbers assigned to each patient-tablet.
The medical doctor can virtually call up the next patient in line for preanesthesiologic assessment.
After the examination both medical doctors and patients complete a brief questionaire regarding educational level, usability and overall satisfaction
Undersøgelsestype
Observationel
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
5 år og ældre (Barn, Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
Male and female patients (aged > 4 years) for elective surgery
Beskrivelse
Inclusion Criteria:
- Male and female patients of all ages
- Elective surgical procedure
Exclusion Criteria:
- Language inabilities (German)
- Severe hearing - loss and visual impairment
- In-Patient care > 24 h
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Waiting time in the anesthesia admissions ambulance
Tidsramme: Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
The waiting time will be measured in hours and minutes
|
Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Study patient satisfaction
Tidsramme: Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
The question "How satisfied is the Patient?" is measured during stay in the anesthesia admissions ambulance.This scale ranges from -3 to +3, contains no "0"(forced-choice).
|
Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
|
Medical doctor statisfaction
Tidsramme: Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 day
|
The question "How satisfied is the medical doctor?" is measured during stay in the anesthesia admissions ambulance.This scale ranges from -3 to +3, contains no "0"(forced-choice).
|
Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 day
|
|
Tablet - acceptance by study patients
Tidsramme: Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
The acceptance is measured by a scale ranges from -3 to +3, contains no "0"(forced-choice).
|
Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 hour
|
|
Tablet - acceptance by medical doctor
Tidsramme: Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 day.
|
The acceptance is measured by a scale ranges from -3 to +3, contains no "0"(forced-choice).
|
Participants will be followed for the duration of ambulation ambulance stay, an expected average of 1 day.
|
|
Duration of examination time
Tidsramme: Participants will be followed for the duration of examinationin the ambulance, an expected average of 1 hour.
|
The duration of examination time will be measured in hours and minutes.
|
Participants will be followed for the duration of examinationin the ambulance, an expected average of 1 hour.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Studieleder: Claudia Spies, MD, Prof., Department of Anesthesiology and Intensive Care Medicine Berlin, Charité - Univeristy Medicine Berlin
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. juni 2015
Primær færdiggørelse (Forventet)
1. september 2015
Studieafslutning (Forventet)
1. oktober 2015
Datoer for studieregistrering
Først indsendt
20. marts 2015
Først indsendt, der opfyldte QC-kriterier
28. maj 2015
Først opslået (Skøn)
29. maj 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
31. juli 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
30. juli 2015
Sidst verificeret
1. juli 2015
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- Anaest-App
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 .