Study to Implement Shared Decision-Making Intervention in Practice for Chest Pain

Overview

Información sobre este estudio

The purpose of this study is to incorporate the Chest Pain Choice decision aid in a stakeholder-guided evidence-based clinical practice pathway, to implement it in practice, and to evaluate its effects — potential to improve patients’ experience of care while simultaneously limiting unnecessary healthcare utilization and improving population health.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria - Sample Cohort:

  • Date of service within 1 year of implementing the CPC-pathway at each site (the prior year)
  • Patient age 30+
  • Visit was diagnosed as nontraumatic chest pain
  • First troponin result was <99th percentile
  • A sample cohort will be taken again at the end of the study for the 12-month period during the intervention phase, and the inclusion criteria will be the same.
  • At 60-days post-discharge, we will review the medical record to determine whether the participant has returned to the Emergency Department, had other visits with the participating health system, and to assess 60-day mortality status. If 60-day mortality status is not available within the health system’s medical records, we will acquire 60-day mortality data from Accurint, a national database used by debt collection agencies, to assess mortality status.

Inclusion Criteria - Intervention Group (survey participants):

  • Date of service is during intervention phase
  • Patient age 30+
  • Chief complaint or ED diagnosis is nontraumatic chest pain
  • First troponin result is <99th percentile

Inclusion Criteria - Focus Group:

  • Physicians and Residents of participating Departments of Emergency Medicine, as well as Nurses and Managers working in the same

Inclusion Crteria - Clinicans:

  • Physicians and Residents from the participating Departments of Emergency Medicine

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Casey Clements, M.D., Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20502529

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