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An Intervention to Improve Implantable Cardioverter-Defibrillator Deactivation Conversations (WISDOM)

Primary Purpose

Communication, Heart Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Communication training for cardiologists.
Control arm
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Communication focused on measuring Heart failure, Palliative care, Communication

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Clinicians:

  • At all sites, a core group of approximately 10 heart failure clinicians (physicians, nurses) care exclusively for patients with advanced heart failure in both inpatient and outpatient settings; all of these clinicians are eligible..

Patients:

  • Patient does not currently have a ventricular assist device
  • Age > 18
  • Fluent in English
  • Consistent and reliable access to a phone

For Inpatient:

  • Has had at least 1 other heart failure in the last year, OR
  • Meets all three of the following criteria at time of admission:

    1. BUN > 43
    2. SBP ≤ 115
    3. CR > 2.75 OR
  • Was on inotropes OR intravenous diuretics OR intravenous heart failure treatments in emergency department OR in outpatient setting prior to the current hospital admission

For Outpatient

  • Has had 2 or more heart failure related admissions in the last year OR
  • Has class IV heart failure in the outpatient setting OR
  • Has Class III heart failure in outpatient setting AND 1 heart failure related admission in the last year OR
  • Has Class III heart failure in outpatient setting AND 2 of the following 4 conditions:

    1. Age ≥ 70
    2. BUN ≥ 43
    3. Cr ≥ 2.75
    4. SBP≤115 OR
  • Is on inotropes (e.g., dobutamine, milrinone) OR intravenous diuretics OR intravenous heart failure treatments in emergency department OR in outpatient setting

Caregivers:

  • Age > 18
  • Fluent in English
  • Consistent and reliable access to a phone

Exclusion Criteria for patients:

  • Not having an ICD

Sites / Locations

  • University of Colorado - Denver
  • Yale New-Haven Hospital
  • Mayo Medical Center
  • Montefiore Medical Center
  • Icahn School of Medicine at Mount Sinai
  • Hospital of the University of Pennsylvania

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Communication training for cardiologists

Control arm

Arm Description

The intervention consists of an educational workshop for heart failure physicians, a reminder system, and a system providing aggregated feedback on their conversations with patients about ICD deactivation.

Cardiology grand rounds will be held at usual care sites on the importance of advance care planning.

Outcomes

Primary Outcome Measures

Prevalence of Conversations about ICD Deactivation
Whether deactivation discussion occurred difference between 1st and 3rd clinical encounters after enrollment
Prevalence of Conversations about ICD Deactivation
Whether deactivation discussion occurred difference between 1st and 3rd clinical encounters after enrollment
Prevalence of Conversations about ICD Deactivation
Whether deactivation discussion occurred difference between 3 and 9 months after enrollment
Prevalence of Conversations about ICD Deactivation
Whether deactivation discussion occurred difference between 3 and 9 months after enrollment

Secondary Outcome Measures

Prevalence of ICD Deactivation
Whether ICD deactivation occurred difference between 1st and 3rd clinical encounters after enrollment
Prevalence of ICD Deactivation
Whether ICD deactivation occurred difference between 1st and 3rd clinical encounters after enrollment
Prevalence of ICD Deactivation
Whether ICD deactivation occurred difference between 3 and 9 months after enrollment
Prevalence of ICD Deactivation
Whether ICD deactivation occurred difference between 3 and 9 months after enrollment
Psychological Outcomes in Bereaved Caregivers
Psychological Outcomes in Bereaved Caregivers

Full Information

First Posted
October 13, 2011
Last Updated
October 5, 2016
Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), University of Colorado, Denver, Mayo Clinic, University of Pennsylvania, Oregon Health and Science University, Montefiore Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01459744
Brief Title
An Intervention to Improve Implantable Cardioverter-Defibrillator Deactivation Conversations
Acronym
WISDOM
Official Title
An Intervention to Improve ICD Deactivation Conversations (WISDOM - Working to Improve discuSsions About DefibrillatOr Management)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), University of Colorado, Denver, Mayo Clinic, University of Pennsylvania, Oregon Health and Science University, Montefiore Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
An Implantable Cardioverter-Defibrillator (ICD) is a device implanted in a patient's chest to monitor the heart rhythm and deliver shocks to terminate potentially lethal arrhythmias when necessary. While ICDs reduce sudden cardiac death, patients with ICDs eventually die of heart failure or other diseases. As patients near the end of life, physiologic changes (intrinsic and extrinsic to the heart) may affect the cardiac conduction system, leading to more arrhythmias and increasing the frequency of shocks. Because ICD shocks can cause pain and anxiety and may not prolong a life of acceptable quality, it is appropriate to consider deactivating the shocking function of ICDs as patients' clinical status worsens and death is near. This will be a randomized controlled trial of a physician centered counseling and education intervention to improve clinician-patient communication about the management of ICDs.
Detailed Description
An Implantable Cardioverter-Defibrillator (ICD) is a device implanted in a patient's chest to monitor the heart rhythm and deliver shocks to terminate potentially lethal arrhythmias when necessary. While ICDs reduce sudden cardiac death, patients with these devices do eventually die, either of heart failure or other chronic diseases. As a patient's disease worsens, physiologic changes (intrinsic and extrinsic to the heart) may affect the cardiac conduction system, leading to more arrhythmias and increasing the frequency of shocks. Because ICD shocks can cause pain and anxiety and may not prolong a life of acceptable quality, it is appropriate to consider ICD deactivation as a patient's clinical status worsens and death is near. However, these conversations rarely occur. The investigators propose to conduct a randomized clinical trial of a physician-centered patient counseling and support intervention to improve communication between cardiologists and patients with ICDs. The goals of the study are to determine the effectiveness of the intervention to: 1) increase conversations about ICD deactivation, 2) increase the number of patients who have their devices deactivated, and 3) improve mental health outcomes for bereaved caregivers of deceased patients. The unit of randomization is the hospital, the intervention is aimed at cardiologists, and the unit of analysis is the patient. The investigators have created a network of six academic medical centers across the country. The intervention to be delivered consists of three parts. First, the PI will conduct a workshop on communication specific to ICD-deactivation with cardiologists at the intervention centers. Second, when enrolled patients are admitted to the hospital or seen in the outpatient setting, the cardiologist will receive two reminders (one via email, one in the patient chart) that the patient is appropriate for a conversation about ICD deactivation. Finally, cardiologists will receive aggregated feedback about the number of conversations they have conducted and data on patients' satisfaction with conversations every six months. Physicians at usual care hospitals receive a didactic lecture on advance care planning. All patients and surrogates will be interviewed at baseline and then assessed at regular intervals to determine the outcomes of: 1) the prevalence of conversations about ICD deactivation as reported by the patient/surrogate; and 2) the frequency with which patients have their devices deactivated. Caregivers will continue to be interviewed at regular intervals up to 6 months after the patient dies to determine the relationship of the intervention to caregiver mental health outcomes. Given the exponential increase in the number of patients with ICDs, this intervention has the potential to improve the quality of care for thousands of patients near the end of life and their families.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Communication, Heart Failure
Keywords
Heart failure, Palliative care, Communication

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
562 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Communication training for cardiologists
Arm Type
Experimental
Arm Description
The intervention consists of an educational workshop for heart failure physicians, a reminder system, and a system providing aggregated feedback on their conversations with patients about ICD deactivation.
Arm Title
Control arm
Arm Type
Placebo Comparator
Arm Description
Cardiology grand rounds will be held at usual care sites on the importance of advance care planning.
Intervention Type
Behavioral
Intervention Name(s)
Communication training for cardiologists.
Intervention Description
Communication training: a 90 minute workshop to discuss ways to improve communication in patients with serious illness. Reminders to Cardiologists. Cardiologists will receive reminders to prompt them to have conversations relating to ICD management with patients enrolled in the study. Audit and feedback. Cardiologists will receive feedback on their rates of conversation as well as data on patient/family satisfaction with their communication skills.
Intervention Type
Other
Intervention Name(s)
Control arm
Intervention Description
Cardiology grand rounds will be held at usual care sites on the importance of advance care planning.
Primary Outcome Measure Information:
Title
Prevalence of Conversations about ICD Deactivation
Description
Whether deactivation discussion occurred difference between 1st and 3rd clinical encounters after enrollment
Time Frame
after 1st clinical encounter after enrollment for intervention group
Title
Prevalence of Conversations about ICD Deactivation
Description
Whether deactivation discussion occurred difference between 1st and 3rd clinical encounters after enrollment
Time Frame
3rd clinical encounter after enrollment for intervention group
Title
Prevalence of Conversations about ICD Deactivation
Description
Whether deactivation discussion occurred difference between 3 and 9 months after enrollment
Time Frame
3 months after enrollment for control group
Title
Prevalence of Conversations about ICD Deactivation
Description
Whether deactivation discussion occurred difference between 3 and 9 months after enrollment
Time Frame
9 months after enrollment for control group
Secondary Outcome Measure Information:
Title
Prevalence of ICD Deactivation
Description
Whether ICD deactivation occurred difference between 1st and 3rd clinical encounters after enrollment
Time Frame
After 1st encounter after enrollment for intervention group
Title
Prevalence of ICD Deactivation
Description
Whether ICD deactivation occurred difference between 1st and 3rd clinical encounters after enrollment
Time Frame
After 3rd encounter after enrollment for intervention group
Title
Prevalence of ICD Deactivation
Description
Whether ICD deactivation occurred difference between 3 and 9 months after enrollment
Time Frame
After 3 months after enrollment for control group
Title
Prevalence of ICD Deactivation
Description
Whether ICD deactivation occurred difference between 3 and 9 months after enrollment
Time Frame
After 6 months after enrollment for control group
Title
Psychological Outcomes in Bereaved Caregivers
Time Frame
4 weeks after patient death
Title
Psychological Outcomes in Bereaved Caregivers
Time Frame
6 months after patient death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinicians: At all sites, a core group of approximately 10 heart failure clinicians (physicians, nurses) care exclusively for patients with advanced heart failure in both inpatient and outpatient settings; all of these clinicians are eligible.. Patients: Patient does not currently have a ventricular assist device Age > 18 Fluent in English Consistent and reliable access to a phone For Inpatient: Has had at least 1 other heart failure in the last year, OR Meets all three of the following criteria at time of admission: BUN > 43 SBP ≤ 115 CR > 2.75 OR Was on inotropes OR intravenous diuretics OR intravenous heart failure treatments in emergency department OR in outpatient setting prior to the current hospital admission For Outpatient Has had 2 or more heart failure related admissions in the last year OR Has class IV heart failure in the outpatient setting OR Has Class III heart failure in outpatient setting AND 1 heart failure related admission in the last year OR Has Class III heart failure in outpatient setting AND 2 of the following 4 conditions: Age ≥ 70 BUN ≥ 43 Cr ≥ 2.75 SBP≤115 OR Is on inotropes (e.g., dobutamine, milrinone) OR intravenous diuretics OR intravenous heart failure treatments in emergency department OR in outpatient setting Caregivers: Age > 18 Fluent in English Consistent and reliable access to a phone Exclusion Criteria for patients: Not having an ICD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nathan E. Goldstein, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Colorado - Denver
City
Denver
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Yale New-Haven Hospital
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06510
Country
United States
Facility Name
Mayo Medical Center
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10023
Country
United States
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10601507
Citation
Buxton AE, Lee KL, Fisher JD, Josephson ME, Prystowsky EN, Hafley G. A randomized study of the prevention of sudden death in patients with coronary artery disease. Multicenter Unsustained Tachycardia Trial Investigators. N Engl J Med. 1999 Dec 16;341(25):1882-90. doi: 10.1056/NEJM199912163412503. Erratum In: N Engl J Med 2000 Apr 27;342(17):1300.
Results Reference
background
PubMed Identifier
8960472
Citation
Moss AJ, Hall WJ, Cannom DS, Daubert JP, Higgins SL, Klein H, Levine JH, Saksena S, Waldo AL, Wilber D, Brown MW, Heo M. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for ventricular arrhythmia. Multicenter Automatic Defibrillator Implantation Trial Investigators. N Engl J Med. 1996 Dec 26;335(26):1933-40. doi: 10.1056/NEJM199612263352601.
Results Reference
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PubMed Identifier
11907286
Citation
Moss AJ, Zareba W, Hall WJ, Klein H, Wilber DJ, Cannom DS, Daubert JP, Higgins SL, Brown MW, Andrews ML; Multicenter Automatic Defibrillator Implantation Trial II Investigators. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction. N Engl J Med. 2002 Mar 21;346(12):877-83. doi: 10.1056/NEJMoa013474. Epub 2002 Mar 19.
Results Reference
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PubMed Identifier
15659722
Citation
Bardy GH, Lee KL, Mark DB, Poole JE, Packer DL, Boineau R, Domanski M, Troutman C, Anderson J, Johnson G, McNulty SE, Clapp-Channing N, Davidson-Ray LD, Fraulo ES, Fishbein DP, Luceri RM, Ip JH; Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT) Investigators. Amiodarone or an implantable cardioverter-defibrillator for congestive heart failure. N Engl J Med. 2005 Jan 20;352(3):225-37. doi: 10.1056/NEJMoa043399. Erratum In: N Engl J Med. 2005 May 19;352(20):2146.
Results Reference
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PubMed Identifier
11297981
Citation
Glikson M, Friedman PA. The implantable cardioverter defibrillator. Lancet. 2001 Apr 7;357(9262):1107-17. doi: 10.1016/S0140-6736(00)04263-X.
Results Reference
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PubMed Identifier
12000634
Citation
Eckert M, Jones T. How does an implantable cardioverter defibrillator (ICD) affect the lives of patients and their families? Int J Nurs Pract. 2002 Jun;8(3):152-7. doi: 10.1046/j.1440-172x.2002.00357.x.
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PubMed Identifier
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Citation
Sears SF Jr, Conti JB. Quality of life and psychological functioning of icd patients. Heart. 2002 May;87(5):488-93. doi: 10.1136/heart.87.5.488. No abstract available.
Results Reference
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PubMed Identifier
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Citation
Gelfman LP, Sudore RL, Mather H, McKendrick K, Hutchinson MD, Lampert RJ, Lipman HI, Matlock DD, Swetz KM, Pinney SP, Morrison RS, Goldstein NE. Prognostic Awareness and Goals of Care Discussions Among Patients With Advanced Heart Failure. Circ Heart Fail. 2020 Sep;13(9):e006502. doi: 10.1161/CIRCHEARTFAILURE.119.006502. Epub 2020 Sep 2.
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PubMed Identifier
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Citation
Goldstein NE, Mather H, McKendrick K, Gelfman LP, Hutchinson MD, Lampert R, Lipman HI, Matlock DD, Strand JJ, Swetz KM, Kalman J, Kutner JS, Pinney S, Morrison RS. Improving Communication in Heart Failure Patient Care. J Am Coll Cardiol. 2019 Oct 1;74(13):1682-1692. doi: 10.1016/j.jacc.2019.07.058.
Results Reference
derived

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An Intervention to Improve Implantable Cardioverter-Defibrillator Deactivation Conversations

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