- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07572448
The Relationship Between Nurses' Perception Of Safety Culture And Patients' Sense Of Safety
An Investigation Of The Relationship Between Day Surgery Nurses' Perception Of Safety Culture And Patients' Level Of Feeling Safe During Surgery
This study will be conducted to determine the relationship between the perception of safety culture among healthcare professionals working in an outpatient surgical unit and the level of safety patients feel during surgery performed under local anesthesia.
The study population consists of healthcare professionals (N = 140) working in the Day Surgery Unit of Bursa Uludağ University Faculty of Medicine Hospital and patients undergoing procedures. The sample size calculation for the healthcare professionals to be included in the study was determined using the known population sampling method. Using the Raosoft sampling method, with a 5% margin of error and a 95% confidence interval, the minimum required sample size (n) was calculated to be 103. It was decided that the study would include healthcare professionals and patients in a 1:1 ratio. Therefore, the total sample size was calculated to be 206.
Data will be collected using the Hospital Survey on Patient Safety Culture (Version 2.0) and the Feeling Safe During Surgery Scale.
Aperçu de l'étude
Statut
Les conditions
Type d'étude
Inscription (Estimé)
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Currently working as a healthcare professional in an outpatient surgical unit,
- No visual, auditory, or psychological impairments that would prevent them from completing the questionnaires and scales,
- At least a graduate of a vocational high school for healthcare professions,
- Patients scheduled for elective surgery under local anesthesia,
- Patients and nurses who voluntarily agreed to participate in the study.
Exclusion Criteria:
- Refusal to voluntarily participate in the study,
- Presence of any visual, auditory, or psychological impairments that would prevent the completion of questionnaires and scales,
- Individuals who are not healthcare professionals.
- Patients undergoing emergency surgical procedures or those under general anesthesia.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Nurses' level of patient safety culture
Délai: From the registration phase to the end of the approximately 52-week data collection process
|
It will be calculated using scores from the sub-dimensions of the Hospital Survey on Patient Safety Culture (Version 2.0).
|
From the registration phase to the end of the approximately 52-week data collection process
|
|
Patients' Sense of Safety
Délai: From the registration phase to the end of the approximately 52-week data collection process
|
The score range on the Patient Safety During Surgery Scale is 13-130 points.
|
From the registration phase to the end of the approximately 52-week data collection process
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- 2026-6
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .