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Innovative Tool to Limit Spread of COVID 19 in Residential Aged Care Facilities

4. marts 2021 opdateret af: The University of Queensland

Innovative Tool to Limit Spread of COVID 19 in Residential Aged Care

This project is a randomised trial in order to determine if "gamification" can result in behaviour change for healthcare workers in the residential aged care setting. The app is for Age Care and care workers at the front line who are working to protect those most vulnerable to COVID-19. There are 2 groups in this trial on group will receive current and accurate information from an app. The other group will receives the app with the addition of a gamification competent, this will include rewarding experiences for staff doing safety behaviours and wellbeing behaviours. The purpose of the gamification is to create a calming and reassuring experience that injects positivity and joy where possible during this stressful time.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

The study design will be a multi- centre cluster randomised control trial, where Age Care facilities are randomised into two groups:

  1. Newsfeed- gets the app with newsfeed only
  2. Gamification group- gets the full gamified app, including the newsfeed Workers in our network of residential aged care facilities will be invited to participate in a study of communication of information regarding COVID-19 and how they will play a role in preventing its spread.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

34

Fase

  • Ikke anvendelig

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

18 år til 90 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Age Health Care Worker

Exclusion Criteria:

-

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Newsfeed
This will provide you with reliable accurate information on the pandemic.
Adfærdsmæssigt: Newsfeed function
This will provide the user with reliable accurate information on the pandemic.
Eksperimentel: Gamification
The gamification function will allow users to earn points for actions completed. The gamification function has links to resources for infection control, watching or completing tasks or playing games to earn points. Points can be viewed at a facility level, state level or national level.
Adfærdsmæssigt: Gamification
This will provide the user with the newsfeed function and the addition of a gamification function

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
To compare the hours of sick leave used over the course of the 4-week period post randomisation for each group
Tidsramme: 4 weeks
Compare the number of sick leave prior to users utilising the app and at the end of the 4 weeks between the arms
4 weeks

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
To compare handwashing behaviour
Tidsramme: 4 weeks
Compare the amount of soap/sanitiser used between the arms
4 weeks
To compare self-testing rates
Tidsramme: 4 weeks
Compare the number of self tests between the two arms
4 weeks
To compare the level of surface wipe down
Tidsramme: 4 weeks
Compare the amount of wipes/disinfectant used between the two arms
4 weeks
To compare number of COVID-19 tests completed in Facilities
Tidsramme: 4 weeks
Compare the number of COVID-19 tests between the two arms
4 weeks
To compare the number of COVID 19 infections in facilities
Tidsramme: 4 weeks
Compare the number of COVID-19 infections between the arms
4 weeks
To compare the other types of outbreaks (Flu, gastroenteritis)
Tidsramme: 4 weeks
Compare the number of flu and gastroenteritis outbreaks between the arms
4 weeks
To compare the awareness of COVID 19 training available to workers in the facilities
Tidsramme: 4 weeks
Compare the COVID 19 training between the two arms, this is via a self reported survey
4 weeks
To compare the awareness of PPE training available to workers in the facilities
Tidsramme: 4 weeks
Compare the awareness of PPE training of the workers in the two arms, this is captured in self reported survey
4 weeks
To compare the levels of PPE material used in
Tidsramme: 4 weeks
Compare the amount of PPE used between the arms
4 weeks
To compare the wellbeing and self-efficacy of the two groups
Tidsramme: 4 weeks
Compare the wellbeing and self-efficacy between the two arms, this is captured in a self reported survey.
4 weeks

Samarbejdspartnere og efterforskere

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

Sponsor

The University of Queensland

Efterforskere

  • Ledende efterforsker: David L Paterson, PhD, The University of Queensland

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 (Faktiske)

6. maj 2020

Primær færdiggørelse (Faktiske)

26. august 2020

Studieafslutning (Faktiske)

26. august 2020

Datoer for studieregistrering

Først indsendt

4. maj 2020

Først indsendt, der opfyldte QC-kriterier

4. maj 2020

Først opslået (Faktiske)

6. maj 2020

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. marts 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

4. marts 2021

Sidst verificeret

1. april 2020

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • Care Collective Study

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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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 .

Kliniske forsøg med Gastroenteritis

Kliniske forsøg med Newsfeed function

Søg i lignende forsøg

Sponsorer og samarbejdspartnere

Medicinske tilstande

Narkotikainterventioner

CROs by country

CROs in Taiwan

Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner