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An Incitative Multifaceted PROcedure for Pneumococcal Vaccination at the Emergency Department (IMPROVED)

22 de enero de 2020 actualizado por: Centre Hospitalier Princesse Grace

An Incitative Multifaceted PROcedure for Pneumococcal Vaccination at the Emergency Department; A Multicenter Prospective Randomized Open Trial The IMPROVED Project

Background :

Community-acquired pneumonia (CAP) is a threat in industrialized countries. It represents the 6th cause of death. CAP also frequently associates with other disorders responsible for admission and death. Among bacteria responsible for CAP, Streptococcus pneumonia is a major pathogen that is commonly involved and frequently leads to severe infection and admission. Categories at risk for this pathogen have been determined, and can be proposed anti-pneumococcal vaccination (APV) that efficiently and safely protects from this microorganism.

In the context of US health services, monocenter pilot experiences have reported improvement of pneumococcal prophylaxis implementing vaccination procedure at ED. A study that set in New Mexico (2003) reported a significant increase in APV (from 18% to 84%) when patients at risk were proposed vaccination at ED. To obtain these results, medical students were specifically trained and dedicated to screen and vaccinate against St. pneumoniae. Another single center trial (Tennessee, 2007) for APV at ED obtained an improvement (from 38.8 to 45.4%) when physicians were alerted for pneumococcal risk by the software they usually utilized at bedside. However these experiences remain sparse as additional dedicated resources are required or patients and attending ED physicians can be reluctant to proceed to vaccination at ED.

Mobile phone and derived communication modalities are current vectors to deliver information in several fields including education and medicine. Initially used in developing countries, short-message services (SMS) have improved behaviour of patients in various medical areas. In France, the investigators have observed that most patients above 50 years of age admitted after ED visit are equipped with mobile phone and can receive alerts by SMS.

These observations prompt us to propose a multifaceted procedure to improve APV after ED visit in at-risk patients, combining structured oral interview, written information and SMS as reminders.

Purpose : The investigators hypothesized that

  • a multifaceted intervention to promote anti-pneumococcal vaccination combining a structured oral interview, a written information to patient and his/her general practitioner, and a series of 3 SMS,
  • improves anti-pneumococcal vaccination at 6 months,
  • in at-risk patients (65+ years) visiting the emergency department. In order to answer this question, the investigators designed an interventional prospective multicenter randomized study (cluster).

Descripción general del estudio

Estado

Terminado

Tipo de estudio

De observación

Inscripción (Actual)

1475

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

      • Clermont-ferrand, Francia, 63003
        • Centre Hospitalier Universitaire de Clermont-Ferrand
      • Issoire, Francia, 63503
        • Centre Hospitalier Paul Ardier
      • Marseille, Francia, 13015
        • AP-HM - Hôpital Nord
      • Marseille, Francia, 13385
        • AP-HM - La Timone
      • Marseille, Francia, 13915
        • Hia Laveran
      • Menton, Francia, 06507
        • Centre Hospitalier La Palmosa
      • Nice, Francia, 06003
        • Centre Hospitalier Universitaire De Nice
      • Orange, Francia, 84106
        • Centre Hospitalier Louis Giorgi
      • Paris, Francia, 75010
        • Hôpital Lariboisière
      • Paris, Francia, 75679
        • Hôpital Cochin
      • Paris, Francia, 75020
        • Hôpital Tenon
      • Paris, Francia, 75018
        • Hôpital Bichat-Claude Bernard
      • Paris, Francia, 75013
        • Hôpital Pitié-Salpêtrière
      • Saint-denis, Francia, 93200
        • Centre Hospitalier de Saint-Denis
      • Vaison-la-romaine, Francia, 84110
        • Centre Hospitalier de Vaison-la-Romaine
      • Valreas, Francia, 84600
        • Centre Hospitalier Jules Niel
      • Vichy, Francia, 03207
        • Centre Hospitalier Jacques Lacarin
      • Monaco, Mónaco, 98000
        • Centre Hospitalier Princesse Grace

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

65 años y mayores (Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra de probabilidad

Población de estudio

patient aged 65 years or over who is not vaccinated against pneumoccocus virus during consultation with medical emergencies

Descripción

Inclusion Criteria:

  • patients 65-year old and above,
  • benefit from French or Monaco social security a social security.

Exclusion Criteria:

  • refuse to participate,
  • no possibility to receive SMS,
  • impaired cognitive functions and mental status precluding understanding of the study,
  • anticipated barriers precluding adequate follow-up (ex. homeless),
  • previous APV,
  • contraindication to APV,
  • do not understand/read French.

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

Cohortes e Intervenciones

Grupo / Cohorte
Multifaceted
  • brief structured interview with the physician about pneumococcal risk and vaccination,
  • information sheet delivered to patients with explanation about risk and benefit of APV,
  • letter given to patient for his/her general practitioner stating that the patient is at-risk for pneumococcal infection and could benefit of APV,
  • 3 SMS every 2 weeks to remind patients talking of pneumococcal risk with general practitioner.
Control
  • information sheet delivered to patients with explanation about the aim of the study,
  • brief interview with the physician about study.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Impact of a multifaceted procedure at ED visit on anti-pneumococcal vaccination. (APV) at 6-month. Evaluation criteria : Δ percentage (%) of APV vaccination at 6-month
Periodo de tiempo: 6 month
6 month

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
On Flu vaccination at 6-month Δ percentage (%)
Periodo de tiempo: 6 month
number of patients receiving vaccination against flu at 6-month. This issue will be collected by phone (patient, relative or general practioner). This will be a declarative data
6 month
On episodes of respiratory tract infections requiring antibiotics or admission at 6-month Δ (absolute number of events)
Periodo de tiempo: 6 month
number of patients who experienced respiratiory tract infection requiring antibiotics or admission. This issue will be collected by phone at 6-month (patient, relative or general practioner). This will be a declarative data
6 month
On death at 6- and 12-month (absolute number of events)
Periodo de tiempo: 6 month
6 month
On death related to infection at 6- and 12-month (absolute number of events)
Periodo de tiempo: 6 month
6 month
Psychosocial evaluation of patients and acceptance / refusal of vaccination
Periodo de tiempo: 6 month
The patient will fil a Psychosocial evaluation questionnaire during the ED visit. To achieve this issue, we will use the socio-economic indicators mobilized in investigations in social epidemiology: sex, age, education, occupation, housing, income and household size. This composite questionnaire will be used for qualitative analysis.
6 month

Colaboradores e Investigadores

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

Investigadores

  • Director de estudio: Yann-Erick CLAESSENS, MD-PhD, Centre Hospitalier Princesse Grace
  • Director de estudio: Xavier DUVAL, MD-PHD, Groupe Hospitalier Bichat Claude-Bernard
  • Director de estudio: José LABARERE, MD, University Hospital, Grenoble
  • Director de estudio: Jocelyn RAUDE, PHD, Ecole des Hautes Etudes en Santé Publique

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)

1 de noviembre de 2015

Finalización primaria (Actual)

1 de octubre de 2016

Finalización del estudio (Actual)

1 de octubre de 2017

Fechas de registro del estudio

Enviado por primera vez

4 de julio de 2013

Primero enviado que cumplió con los criterios de control de calidad

11 de julio de 2013

Publicado por primera vez (Estimar)

15 de julio de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

23 de enero de 2020

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

22 de enero de 2020

Última verificación

1 de octubre de 2017

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

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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