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Decision Aid for Shared Decision Making in Acute Respiratory Failure

Overview

Información sobre este estudio

The purpose of this study is to develop, in close collaboration with stakeholders, an evidence-based decision aid for patients with acute respiratory failure.  To evaluate the impact of the decision aid on patient-important outcomes. We will conduct a prospective trial assessing the impact of the decision aid (vs. usual specialist care) on patient knowledge, patient involvement in decision-making, decision quality, treatment choice, and patient outcomes.

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: 

Observations of Clinical Encounters and Field Testing & Iterative Development

  • Clinician
    • ICU nurse or ICU physician (resident, fellow, consultant) at Mayo Clinic, Rochester
  • Patient
    • Adults ≥ 18 years
    • ICU patient
    • Diagnosis of acute respiratory failure (defined as use of supplemental oxygen, noninvasive mechanical ventilation or invasive mechanical ventilation)
  • Family member
    • Adults ≥ 18 years
    • Family member of ICU patient with acute respiratory failure

Initial Prototype Focus Group Input

  • Patients
    • Adults ≥ 18 years
    • ICU patient
    • Diagnosis of acute respiratory failure (defined as use of supplemental oxygen, noninvasive mechanical ventilation or invasive mechanical ventilation)
  • Family member
    • Adults ≥ 18 years
    • Family member of current ICU patient with acute respiratory failure
  • Patient Advisory Group Member
    • Adults ≥ 18 years
    • Member of the patient advisory group at Mayo Clinic Rochester
  • Clinician
    • ICU nurse or ICU physician (resident, fellow, consultant) at Mayo Clinic, Rochester

Exclusion Criteria:

Observations of Clinical Encounters and Field Testing & Iterative Development

  • Clinician
    • None
  • Patient
    • Major barriers to participate in shared decision making or to providing informed consent (i.e. dementia, severe hearing or visual impairment)
    • Prisoners
  • Family member
    • Major barriers to participate in shared decision making or to providing informed consent (i.e. dementia, severe hearing or visual impairment)

Initial Prototype Focus Group Input

  • Patients
    • Major barriers to participate in shared decision making or to providing informed consent (i.e. dementia, severe hearing or visual impairment)
    • Prisoners
  • Family member
    • Major barriers to participate in shared decision making or to providing informed consent (i.e. dementia, severe hearing or visual impairment)
  • Patient Advisory Group Member
    • Major barriers to participate in shared decision making or to providing informed consent (i.e. dementia, severe hearing or visual impairment)
  • Clinician
    • None

 

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

Ognjen Gajic, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20310576

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