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Patient Perception on the Role of Anesthesiologists

1 de abril de 2019 actualizado por: Stessel Björn, Jessa Hospital

Patient Perception on the Role of Anesthesiologists: a Survey on the Belgian Perspective

Previous studies showed that the role of the anesthesiologist, their education and role within the hospital is not known by the general public. The lack of knowledge about anesthesia can be an important factor in patients' fear before the planned surgery and can therefore impact patient's general satisfaction. By means of a survey in patients planned for elective surgery, the investigators want to investigate the perception of patients regarding the anesthesiologist, their education and role within the hospital, the general knowledge of the patient regarding anesthesia and possible pre-operative fears and concerns.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

Introduction:

Previous studies, mainly performed in the USA and a few in Europe, showed that the role of the anesthesiologist, their education and role within the hospital is not known by the general public (1). Other studies questioned the expectations as well as fear of patients with respect to anesthesia (2). The lack of knowledge about the anesthesia can be an important factor in patients' fear before the planned surgery and can therefore impact patient's general satisfaction. While studies have been performed in several countries, not a single study as far as the investigators know, has been performed in Belgium. Given the fact that the anesthesiologist plays an important role during all stages of surgery (pre-, per-, post-operative), it is important to know how patients experience anesthesia and the role of the anesthesiologist. In this way, possible points of attention can be explored which can lead to a better patient satisfaction in the future.

Outcome measures:

With this study, the investigators want to investigate the perception of patients regarding the anesthesiologist, their education and role within the hospital, the general knowledge of the patient regarding anesthesia and possible pre-operative fears and concerns.

The investigators will determine these outcome measures by performing a survey (standardized questions) which will investigate the following 8 parts:

  • Patient demographics
  • The perception of the role and educational training of the anesthesiologist
  • The role of the anesthesiologist in the hospital
  • General knowledge of anesthesia
  • Trust in medical specialist and anesthesiologist
  • Fear and concerns about anesthesia
  • Patients' expectation regarding recovery and postoperative pain
  • Information for the anesthesiologist and possible points of improvement

Design:

In this monocentric, investigator-initiated, observational, cohort-study, the investigators will perform a survey in all patients that are planned to undergo elective surgery, both ambulatory as well as inpatient surgery. This study will be performed according to the Declaration of Helsinki and will be approved by the Ethical Committee of the Jessa Hospital before the start of the study. A written informed consent will be obtained before participation in the study.

Study Procedures:

Patients that are planned for elective surgery, both ambulatory and inpatient surgery, will be contacted by a researcher prior to the surgery and asked to participate in the study. After a written informed consent is obtained, the survey will be performed by a single researcher, to minimize inter-individual variability. During the survey, family or other people present in the hospital room are not allowed to help the patient. In hospital rooms where more than 1 patient is present, the survey will be performed only once.

Statistical analysis:

Based on previous, comparable studies (1,3,4), 350 patients will be included in this study. Descriptive statistics will be presented as frequencies and percentages of the total amount of patients for categorical variables, while numerical variables will be presented as mean ± SD. Multiple linear regression analysis and correlations will be calculated (depending on normality). A p-value <0.05 is considered statistical significant, while p<0.10 is considered a tendency.

Tipo de estudio

De observación

Inscripción (Actual)

350

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Hasselt, Bélgica, 3500
        • Jessa Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

All patients from the Jessa Hospital, that are planned for elective surgery (both ambulatory and inpatient surgery)

Descripción

Inclusion Criteria:

  • Males and females ≥ 18 years of age
  • American Society of Anesthesiology (ASA) physical status classification: 1-3
  • Patients planned to undergo surgery (both ambulatory and inpatient surgery)
  • Patients that speak Dutch, French or English

Exclusion Criteria:

  • Patients that don't speak Dutch, French or English

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The role and educational training of the anesthesiologist
Periodo de tiempo: max 1 hour per survey
The patients' perception of the work and educational training of the anesthesiologist
max 1 hour per survey

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Patient demographics
Periodo de tiempo: max 1 hour per survey
Gender, age, highest education level, nationality, language, medical condition
max 1 hour per survey
The role of the anesthesiologist in the hospital
Periodo de tiempo: max 1 hour per survey
The patients' perception of the workplace of an anesthesiologist in the hospital
max 1 hour per survey
General knowledge of anesthesia
Periodo de tiempo: max 1 hour per survey
The patients' perception of anesthesia in general
max 1 hour per survey
Trust in medical specialist and anesthesiologist
Periodo de tiempo: max 1 hour per survey
The patients' trust in the medical specialist and anesthesiologist
max 1 hour per survey
Fear and concerns about anesthesia
Periodo de tiempo: max 1 hour per survey
The patients' fear and concerns before the surgery
max 1 hour per survey
Recovery and postoperative pain
Periodo de tiempo: max 1 hour per survey
Several questions regarding the patients' expectation of recovery and postoperative pain
max 1 hour per survey
Information for the anesthesiologist and possible points of improvement
Periodo de tiempo: max 1 hour per survey
Possible points of improvement for the anesthesiologist
max 1 hour per survey

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Björn Stessel, MD, PhD, Jessa Hospital, Dep. of Anesthesiology

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

29 de enero de 2018

Finalización primaria (Actual)

30 de diciembre de 2018

Finalización del estudio (Actual)

30 de diciembre de 2018

Fechas de registro del estudio

Enviado por primera vez

11 de enero de 2018

Primero enviado que cumplió con los criterios de control de calidad

19 de enero de 2018

Publicado por primera vez (Actual)

26 de enero de 2018

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de abril de 2019

Última actualización enviada que cumplió con los criterios de control de calidad

1 de abril de 2019

Última verificación

1 de abril de 2019

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 18.04/anesth18.01

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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