- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02703701
Role of Provider-at-Triage on ED Efficiency and Quality of Care (MD at Triage)
Effects of Provider-at-Triage on Emergency Department Efficiency, Information Delivery and Patient Satisfaction
The United States spends over $8,000 per capita annually on health care and its health care system is more expensive than other developed countries. Even with high per capita costs and a high proportion of physician specialists, the US lags in health care performance from patients' perspectives.
The hospital emergency department (ED) is often the portal of entry for patients seeking health care services and is therefore an ideal setting for initiatives to improve efficiency of care delivery and patient satisfaction. Reduction in wait times, enhanced information delivery and ED staff service quality all have a positive influence on patient perception of health care quality and satisfaction.
Prior studies have attempted to increase patient satisfaction by improving staff communication and courtesy, implementing a patient satisfaction team in triage, and delivering information to patients in a timely manner. Another strategy to increase the efficiency of ED operations is adding a physician to triage to perform brief medical screenings and initiate necessary patient testing and treatment. This contrasts to usual practice in which physicians evaluate patients only following registration and nurse assessment of illness or injury severity.
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
This study will assess the impact of early patient assessment by a physician at Emergency Department (ED) triage on patient perception of information delivery, overall patient satisfaction and ED efficiency. ED efficiency will be assessed by ED length of patient stay, ED left-without-being-seen and ED left during treatment rates.
Participants who decide to take part in this study, will be asked questions by research staff, who will document responses on a secure iPAD device. The survey will ask participants how they feel about their health condition, the emergency department wait, the care they received in the emergency department and how satisfied the participant was with the care received.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Florida
-
Gainesville, Florida, Estados Unidos, 32608
- UF Health
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
Participants are eligible to participate in the study if they are:
- English speaking
- Without hemodynamic or respiratory compromise
- Do not have a nurse-assigned triage severity score of Emergency Severity Index 1 (most severe illness or injury score).
Exclusion Criteria:
Participants will be excluded if they are:
- Unwilling or unable to sign an informed consent
- In police custody
- Too ill to participate in study.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
|
Usual Care
Group enrolled during normal emergency department operating procedures (without a physician present at triage).
|
No physician at triage
|
|
Physician at Triage
Group enrolled while a physician is present at triage.
|
A physician embedded at triage
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Patient Satisfaction
Periodo de tiempo: 60 minutes after Emergency Department triage
|
Patient Satisfaction Score- brief survey measured on a Likert Scale
|
60 minutes after Emergency Department triage
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Emergency Department efficiency
Periodo de tiempo: 24 hours after ED triage in minutes
|
Impact of physician at triage on ED length of stay rates
|
24 hours after ED triage in minutes
|
|
Left without being seen rate
Periodo de tiempo: 12 hours after ED triage in minutes
|
Impact of physician at triage on left without being seen rate
|
12 hours after ED triage in minutes
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Brandon Allen, MD, Univeristy of Florida
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- IRB201500586
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .