Online Mindfulness-terapi for pandemisk tretthet og motstandskraft hos COVID-19 sykepleiere
23. mai 2024 oppdatert av: Chimei Medical Center
Evaluering av effekten av online mindfulness-terapi på pandemisk tretthet og motstandskraft blant sykepleiere i COVID-19-karanteneavdelinger
Denne studien evaluerer online mindfulness-terapis innvirkning på pandemisk tretthet og motstandskraft hos sykepleiere i COVID-19-karanteneavdelingen.
60 sykepleiere ble delt inn i forsøks- og kontrollgrupper, hvor forsøksgruppen fikk et 6-ukers online mindfulness-kurs.
Studieoversikt
Status
Fullført
Intervensjon / Behandling
Detaljert beskrivelse
Denne studien evaluerer effektiviteten av online mindfulness-terapi for å redusere pandemisk tretthet og øke motstandskraften blant sykepleiere i COVID-19-karanteneavdelinger.
Ved å bruke et kvasi-eksperimentelt design med gjentatte tiltak ble 60 sykepleiere delt inn i eksperimentelle og kontrollgrupper.
Eksperimentgruppen deltok på et 6-ukers online mindfulness-kurs.
Resultatene ble målt ved hjelp av spørreskjemaer om pandemisk utmattelse og motstandskraft ved pre-testen, tre uker og etter seks uker.
Studietype
Intervensjonell
Registrering (Faktiske)
60
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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其他（非美國）
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Tainan City, 其他（非美國）, Taiwan, 71004
- Chi Mei Medical Center
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inklusjonskriterier:
- Over 20 år gammel.
- Sykepleiere ved dedikerte covid-19-avdelinger og dedikerte intensivavdelinger.
Ekskluderingskriterier:
- Vanskeligheter med å delta
- mindre enn 80 % av det totale antallet online mindfulness-terapiøkter
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: Eksperimentgruppen vil gjennomgå et 6-ukers online mindfulness-kurs
Eksperimentgruppen fikk et 6-ukers online mindfulness-kurs, en gang i uken i 90 minutter hver økt.
Deltakerne fylte ut spørreskjemaer før kurset, i uke 3 og uke 6.
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Eksperimentgruppen fikk et 6-ukers online mindfulness-kurs, en gang i uken i 90 minutter hver økt.
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Ingen inngripen: Kontrollgruppe
Generell rutinemessig omsorg
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Pandemisk tretthet
Tidsramme: 6 uker
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Bruk Lockdown/Pandemic Fatigue Scale (LFS) mål pandemisk tretthet.
Skalaen med totalt 10 punkter måler pandemisk tretthet.
Omfanget av totalskåre på skalaen er 10-50.
Den viser at pandemisk tretthet øker etter hvert som de totale punkter på skalaen øker.
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6 uker
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Motstandsdyktighet
Tidsramme: 6 uker
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Bruk Connor-Davidson Resilience Scale (CD-RISC) mål individuell motstandskraft.
Skalaen med totalt 25 punkter måler motstandskraft.
Skalaens totale poengsum er 0-100.
Den viser at motstandskraften øker ettersom de totale punkter på skalaen øker.
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6 uker
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
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Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
1. oktober 2022
Primær fullføring (Faktiske)
31. mai 2023
Studiet fullført (Faktiske)
31. mai 2023
Datoer for studieregistrering
Først innsendt
23. mai 2024
Først innsendt som oppfylte QC-kriteriene
23. mai 2024
Først lagt ut (Faktiske)
29. mai 2024
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
29. mai 2024
Siste oppdatering sendt inn som oppfylte QC-kriteriene
23. mai 2024
Sist bekreftet
1. mai 2024
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 11112-001
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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