Thérapie de pleine conscience en ligne pour la fatigue et la résilience pandémiques chez les infirmières COVID-19
23 mai 2024 mis à jour par: Chimei Medical Center
Évaluation des effets de la thérapie de pleine conscience en ligne sur la fatigue et la résilience pandémiques parmi les infirmières des services de quarantaine COVID-19
Cette étude évalue l'impact de la thérapie de pleine conscience en ligne sur la fatigue et la résilience pandémiques chez les infirmières des services de quarantaine COVID-19.
Soixante infirmières ont été divisées en groupes expérimentaux et témoins, le groupe expérimental recevant un cours de pleine conscience en ligne de 6 semaines.
Aperçu de l'étude
Statut
Complété
Intervention / Traitement
Description détaillée
Cette étude évalue l'efficacité de la thérapie de pleine conscience en ligne pour réduire la fatigue pandémique et améliorer la résilience des infirmières dans les services de quarantaine COVID-19.
En utilisant une conception quasi-expérimentale à mesures répétées, 60 infirmières ont été divisées en groupes expérimentaux et témoins.
Le groupe expérimental a participé à un cours de pleine conscience en ligne de 6 semaines.
Les résultats ont été mesurés à l'aide de questionnaires sur la fatigue et la résilience pandémiques au pré-test, à trois semaines et après six semaines.
Type d'étude
Interventionnel
Inscription (Réel)
60
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
其他（非美國）
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Tainan City, 其他（非美國）, Taïwan, 71004
- Chi Mei Medical Center
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Critère d'intégration:
- Plus de 20 ans.
- Infirmières des services dédiés au COVID-19 et des unités de soins intensifs dédiées.
Critère d'exclusion:
- Difficulté à y assister
- moins de 80 % du nombre total de séances de thérapie de pleine conscience en ligne
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Le groupe expérimental suivra un cours de pleine conscience en ligne de 6 semaines
Le groupe expérimental a reçu un cours de pleine conscience en ligne de 6 semaines, une fois par semaine pendant 90 minutes à chaque séance.
Les participants ont rempli des questionnaires avant le cours, à la semaine 3 et à la semaine 6.
|
Le groupe expérimental a reçu un cours de pleine conscience en ligne de 6 semaines, une fois par semaine pendant 90 minutes à chaque séance.
|
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Aucune intervention: Groupe de contrôle
Soins généraux courants
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Fatigue pandémique
Délai: 6 semaines
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Utilisez l’échelle de fatigue pandémique/confinement (LFS) pour mesurer la fatigue pandémique.
L’échelle composée de 10 éléments au total mesure la fatigue liée à la pandémie.
La plage des scores totaux de l’échelle est de 10 à 50.
Il montre que la lassitude face à la pandémie augmente à mesure que le nombre total de points de l’échelle augmente.
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6 semaines
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Résilience
Délai: 6 semaines
|
Utilisez l’échelle de résilience Connor-Davidson (CD-RISC) pour mesurer la résilience individuelle.
L'échelle avec un total de 25 éléments mesure la résilience.
La plage des scores totaux de l’échelle est de 0 à 100.
Il montre que la résilience augmente à mesure que le nombre total de points de l’échelle augmente.
|
6 semaines
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
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Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 octobre 2022
Achèvement primaire (Réel)
31 mai 2023
Achèvement de l'étude (Réel)
31 mai 2023
Dates d'inscription aux études
Première soumission
23 mai 2024
Première soumission répondant aux critères de contrôle qualité
23 mai 2024
Première publication (Réel)
29 mai 2024
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
29 mai 2024
Dernière mise à jour soumise répondant aux critères de contrôle qualité
23 mai 2024
Dernière vérification
1 mai 2024
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 11112-001
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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