Decision Aid for Shared Decision Making in Acute Respiratory Failure
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 14-009718
Sponsor Protocol Number: 14-009718
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
- 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
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