Online mindfulness-therapie voor pandemische vermoeidheid en veerkracht bij COVID-19-verpleegkundigen
23 mei 2024 bijgewerkt door: Chimei Medical Center
Evaluatie van de effecten van online mindfulness-therapie op pandemische vermoeidheid en veerkracht onder verpleegkundigen in COVID-19-quarantaineafdelingen
Deze studie evalueert de impact van online mindfulness-therapie op pandemische vermoeidheid en veerkracht bij verpleegkundigen op de COVID-19-quarantaineafdeling.
Zestig verpleegkundigen werden verdeeld in experimentele en controlegroepen, waarbij de experimentele groep een online mindfulnesscursus van zes weken kreeg.
Studie Overzicht
Toestand
Voltooid
Interventie / Behandeling
Gedetailleerde beschrijving
Deze studie evalueert de effectiviteit van online mindfulness-therapie bij het verminderen van pandemische vermoeidheid en het vergroten van de veerkracht onder verpleegkundigen op COVID-19-quarantaineafdelingen.
Met behulp van een quasi-experimenteel ontwerp met herhaalde metingen werden 60 verpleegkundigen verdeeld in experimentele en controlegroepen.
De experimentele groep nam deel aan een online mindfulnesscursus van zes weken.
De resultaten werden gemeten met behulp van vragenlijsten over pandemische vermoeidheid en veerkracht tijdens de pre-test, drie weken en na zes weken.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
60
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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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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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusiecriteria:
- Ruim 20 jaar oud.
- Verpleegkundigen van speciale COVID-19-afdelingen en speciale intensive care-afdelingen.
Uitsluitingscriteria:
- Moeilijkheid om aanwezig te zijn
- minder dan 80% van het totaal aantal online mindfulnesstherapiesessies
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ander
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: De experimentele groep volgt een online mindfulnesscursus van 6 weken
De experimentele groep kreeg een online mindfulnesscursus van zes weken, één keer per week gedurende 90 minuten.
Deelnemers vulden vragenlijsten in vóór de cursus, in week 3 en in week 6.
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De experimentele groep kreeg een online mindfulnesscursus van zes weken, één keer per week gedurende 90 minuten.
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Geen tussenkomst: Controlegroep
Algemene routinezorg
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Pandemische vermoeidheid
Tijdsspanne: 6 weken
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Gebruik de Lockdown/Pandemic Fatigue Scale (LFS) om pandemische vermoeidheid te meten.
De schaal met in totaal 10 items meet pandemische vermoeidheid.
Het bereik van de totaalscores van de schaal is 10-50.
Het laat zien dat pandemische vermoeidheid toeneemt naarmate het totaal aantal punten op de schaal toeneemt.
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6 weken
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Weerstand
Tijdsspanne: 6 weken
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Gebruik de Connor-Davidson Resilience Scale (CD-RISC) om de individuele veerkracht te meten.
De schaal met in totaal 25 items meet veerkracht.
Het bereik van de totaalscores van de schaal is 0-100.
Het laat zien dat de veerkracht toeneemt naarmate het totaal aantal punten op de schaal toeneemt.
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6 weken
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
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Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 oktober 2022
Primaire voltooiing (Werkelijk)
31 mei 2023
Studie voltooiing (Werkelijk)
31 mei 2023
Studieregistratiedata
Eerst ingediend
23 mei 2024
Eerst ingediend dat voldeed aan de QC-criteria
23 mei 2024
Eerst geplaatst (Werkelijk)
29 mei 2024
Updates van studierecords
Laatste update geplaatst (Werkelijk)
29 mei 2024
Laatste update ingediend die voldeed aan QC-criteria
23 mei 2024
Laatst geverifieerd
1 mei 2024
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 11112-001
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .