Terapia consapevole online per l'affaticamento pandemico e la resilienza negli infermieri COVID-19
23 maggio 2024 aggiornato da: Chimei Medical Center
Valutazione degli effetti della terapia di consapevolezza online sull’affaticamento pandemico e sulla resilienza tra gli infermieri nei reparti di quarantena COVID-19
Questo studio valuta l’impatto della terapia di consapevolezza online sull’affaticamento pandemico e sulla resilienza negli infermieri del reparto di quarantena COVID-19.
Sessanta infermieri sono stati divisi in gruppi sperimentali e di controllo, con il gruppo sperimentale che ha ricevuto un corso online di consapevolezza di 6 settimane.
Panoramica dello studio
Stato
Completato
Intervento / Trattamento
Descrizione dettagliata
Questo studio valuta l’efficacia della terapia di consapevolezza online nel ridurre l’affaticamento pandemico e nel migliorare la resilienza tra gli infermieri nei reparti di quarantena COVID-19.
Utilizzando un disegno quasi sperimentale a misure ripetute, 60 infermieri sono stati divisi in gruppi sperimentali e di controllo.
Il gruppo sperimentale ha partecipato a un corso di consapevolezza online di 6 settimane.
I risultati sono stati misurati utilizzando questionari sulla fatica pandemica e sulla resilienza prima del test, tre settimane e dopo sei settimane.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
60
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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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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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
Criterio di inclusione:
- Più di 20 anni.
- Infermieri dei reparti dedicati al COVID-19 e delle unità di terapia intensiva dedicate.
Criteri di esclusione:
- Difficoltà a partecipare
- meno dell’80% del numero totale di sessioni di terapia di consapevolezza online
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Il gruppo sperimentale sarà sottoposto a un corso di consapevolezza online di 6 settimane
Il gruppo sperimentale ha seguito un corso online di consapevolezza di 6 settimane, una volta alla settimana per 90 minuti ogni sessione.
I partecipanti hanno completato i questionari prima del corso, alla settimana 3 e alla settimana 6.
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Il gruppo sperimentale ha seguito un corso online di consapevolezza di 6 settimane, una volta alla settimana per 90 minuti ogni sessione.
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Nessun intervento: Gruppo di controllo
Cure di routine generali
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Stanchezza pandemica
Lasso di tempo: 6 settimane
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Utilizzare la scala Lockdown/Pandemic Fatigue Scale (LFS) per misurare la fatica pandemica.
La scala con un totale di 10 elementi misura la fatica pandemica.
L'intervallo dei punteggi totali della scala è 10-50.
Mostra che la fatica pandemica aumenta all’aumentare dei punti totali della scala.
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6 settimane
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Resilienza
Lasso di tempo: 6 settimane
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Utilizzare la Connor-Davidson Resilience Scale (CD-RISC) per misurare la resilienza individuale.
La scala con un totale di 25 elementi misura la resilienza.
L'intervallo dei punteggi totali della scala è 0-100.
Mostra che la resilienza aumenta all’aumentare dei punti totali della scala.
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6 settimane
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Pubblicazioni generali
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Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
1 ottobre 2022
Completamento primario (Effettivo)
31 maggio 2023
Completamento dello studio (Effettivo)
31 maggio 2023
Date di iscrizione allo studio
Primo inviato
23 maggio 2024
Primo inviato che soddisfa i criteri di controllo qualità
23 maggio 2024
Primo Inserito (Effettivo)
29 maggio 2024
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
29 maggio 2024
Ultimo aggiornamento inviato che soddisfa i criteri QC
23 maggio 2024
Ultimo verificato
1 maggio 2024
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 11112-001
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .