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Decision Aid Feasibility Trial for Families of Critically Ill Stroke Patients

Feasibility Trial of a Goals of Care Decision Aid for Families of Critically Ill Stroke Patients

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04143113
Enrollment
0
Registered
2019-10-29
Start date
2020-07-01
Completion date
2022-06-30
Last updated
2021-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemorrhagic Stroke, Intracerebral Hemorrhage, Ischaemic Stroke With Coma, Ischemic Stroke

Keywords

stroke, hemorrhagic stroke, shared decision making, neurocritical care, decision aid, goals of care, palliative care, family communication, end of life, critical care, neuroICU, patient-centered care

Brief summary

Severe strokes, including large artery acute ischemic stroke and intracerebral hemorrhage, continue to be the leading cause of death and disability in adults in the U.S. Due to concerns for a poor long-term quality of life, withdrawal of mechanical ventilation and supportive medical care with transition to comfort care is the most common cause of death in severe strokes, but occurs at a highly variable rate. Decision aids (DAs) are shared decision-making tools which have been successfully implemented and validated for many other diseases to assist difficult decision making. The investigators have developed a pilot DA for goals-of-care decisions for surrogates of severe, critically ill stroke patients. This was developed through qualitative research using semi-structured interviews in surrogate decision makers of traumatic brain injury patients and physicians, and adapted to severe strokes. The investigators now propose to pilot-test a DA for surrogates of critically ill severe stroke patients in a feasibility trial.

Detailed description

Severe strokes, including large artery acute ischemic stroke and intracerebral hemorrhage, continue to be the leading cause of death and disability in adults in the U.S, accounting for more than 200,000 of the acute brain injury-related deaths in the U.S. annually. Patients with severe strokes are critically ill and most commonly require mechanical ventilation and supportive medical care with artificial nutrition to ensure survival. However, due to concerns for a poor long-term quality of life, withdrawal of mechanical ventilation and supportive medical care with transition to comfort care is by far the most common cause of death in severe strokes but occurs at a highly variable rate at different stroke centers. Shared decision making is a collaborative process that enhances patients' and surrogates' understanding about prognosis, encourages them to actively weigh the risks and benefits of a treatment, and to match them to patient preferences, thereby decreasing decisional conflict and improving decision quality and health related outcomes. Decision aids (DAs) are shared decision-making tools which have been successfully implemented and validated for many other diseases to assist difficult decision making. No DA currently exists for goals-of-care decisions in critically ill severe stroke patients. Such a patient- and family-centered DA has the potential to improve decision-making for critically ill severe stroke patients by ensuring proxies receive consistent, evidence-based prognostication while also addressing patients' preferences and values. The investigators have developed a pilot DA for goals of care decisions by surrogates of critically ill severe stroke patients using qualitative research using semi-structured interviews in surrogate decision makers of traumatic brain injury patients and physicians, followed by an iterative feedback process with feedback by surrogates, physicians, and other stakeholders (ICU nurses), and adaptation to large artery acute ischemic and hemorrhagic stroke. The investigators now propose to pilot-test a DA for surrogates of critically ill severe stroke patients in a feasibility trial.

Interventions

OTHERDecision Aid

Shared decision making tool

Sponsors

Yale University
CollaboratorOTHER
University of Massachusetts, Worcester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Step-wedge design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

≥18 years of age; no upper age limit * Documented health care proxy or legal next of kin of severe stroke patient admitted to the ICU with intracerebral hemorrhage or acute ischemic stroke. * ≥3 days after insult (stabilization period); clinical team may ask study team to wait longer if clinically indicated * Severe stroke patient remains critically ill after 3 days defined as: either intubated and mechanically ventilated, or unable to swallow, needing feeding tube beyond hospital discharge (even if not intubated) * Surrogate is physically present in ICU to receive decision aid and participate in planned family meeting in person (not over phone)

Exclusion criteria

* Devastating severe stroke patient near death * Patient will be extubated and pass swallow evaluation (as deemed by clinical team) * Surrogate is non-English speaking and no interpreter available to translate decision aid (no available validated, translated decision aid version) * Surrogate is illiterate

Design outcomes

Primary

MeasureTime frameDescription
RecruitmentFrom date of approaching surrogate decision maker for consent until the date of the first documented goals-of-care family meeting, assessed up to 1 month after admission.Consent rate
Participation1-36 hours after family meetingProportion of participants who read decision aid and completed worksheet
Retention3 months after goals-of-care decisionNumber of participants who complete follow-up

Secondary

MeasureTime frameDescription
Impact of Events Scale-revisedBaseline, 1-36 hours after family meeting, and 3-months after goals-of-care decisionis a is a validated 15-item instrument, measuring post-traumatic stress disorder (PTSD) symptoms. Total score is the sum of all questions and ranges from 0 to 88, with higher scores indicating worse PTSD symptoms.
Patient-Perceived Centeredness of Care Scale1-36 hours after family meetingis a is a validated 14-item, 4-point Likert scale based test. Its version adapted to surrogates has shown responsiveness in a recent trial of a nurse-driven communication intervention for surrogates in the ICU. It ranges between 1 (very well) to 4 (not at all), and median score is calculated from all questions. Median scores range from 1 to 4, with lower scores indicating more patient- and family-centered care.

Other

MeasureTime frameDescription
Hospital Anxiety and Depression Scale (HADS)Baseline,1-36 hours after family meeting, and 3-monthsis a 14-item, two-domain (depression, anxiety) instrument with reliability and validity among ICU surrogates, which is recommended by consensus guidelines for the prospective measurement of psychological distress among ICU surrogates. Each of the 14 questions are scored between 0 (not at all) and 3 (most of the time), and summed up for a total HADS score, which ranges from 0 to 42, with higher scores indicating worse symptoms. Total HADS 0-7 =normal, 8-10 borderline abnormal, 11-21=abnormal, indicating high anxiety and depression.
Total number of goals-of-care family meetingsThrough discharge from hospital, an average of 4 weeksInvestigators will sum up the total number of goals-of-care meetings at the patient's ICU discharge.
Decisional Conflict Scale1-36 hours after family meetingis a validated scale that measures the personal perception of choosing an option and factors contributing to choice uncertainty. It is a 16-item, 5-item Likert scale with sub-scores for uncertainty, feeling informed, values clarity, decision support and effective decision-making. It ranges from 0 (strongly agree) to 4 (strongly disagree).
Patient's survival status3-months after goals of care decisionInvestigators will record whether the patient is dead or alive.
Patient's modified Rankin Scale3-months after goals of care decisionis a validated scale that measures the degree of disability or dependence in the daily activities of people who have suffered a stroke or other causes of neurological disability. It ranges from 0 (no symptoms at all) to 6 (death).
Cumulative duration of the goals-of-care family meetingsThrough discharge from hospital, an average of 4 weeksInvestigators will track the duration of each goals-of-care meeting. At the patient's ICU discharge, investigators will sum up the cumulative duration of all goals-of-care meetings \[minutes\].
Surrogate Decision Regret Scale3-months after goals of care decisionis a validated scale that measures distress or remorse after a health care decision with high internal consistency. It asks 5 questions and provides a 5-point Likert scale. It ranges between 1 (strongly agree) to 5 (strongly disagree).
Quality of Communications Scale1-36 hours after family meetingis a is a validated 17-item patient-centered instrument widely used in the ICU to assess surrogates' satisfaction of clinician communication about treatments and understanding treatment decisions. It ranges between 0 (poor) to 10 (absolutely perfect). Total score is the sum of all questions and ranges from 0 to 100, with higher scores indicating better communication.
Clinician-surrogate concordance scale scoreBaseline and 1-36 hours after family meetingmeasures prognostic concordance between ICU clinicians and surrogates. Participants from both groups will independently estimate numerically a SABI patient's 6-month survival and return to independence. Concordance is calculated as the absolute value of the difference in prognosis between the surrogate and the clinician, and, therefore, can range from 0 (no concordance) to 100 (full concordance).
AIS/Intracerebral Hemorrhage (ICH) knowledge testBaseline and 1-36 hours after family meetingMedical knowledge about the goals-of-care decision in severe strokes will be assessed using the medical knowledge test, which was adapted to 17 questions about goals-of-care and severe strokes, all of which are addressed in the decision aid. The % correct will be calculated.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026