Decision Aid for Shared Decision Making in Acute Respiratory Failure

Overview

About this study

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.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

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

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Ognjen Gajic, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available
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CLS-20310576

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