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Adverse Childhood Experiences in Patients With Coronary Artery Disease Pilot

Primary Purpose

Adverse Childhood Experiences, Coronary Artery Disease

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Philadelphia ACE Survey
Lifestyle Assessment
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Adverse Childhood Experiences

Eligibility Criteria

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

Inclusion Criteria:

  1. Age ≥18 years at screening
  2. History of (1) acute coronary syndrome (ACS) OR (2) coronary artery disease (CAD) necessitating prior cardiovascular intervention. History of ACS determined by documentation of ST-elevation myocardial infarction or non-ST-segment elevation infarction 1-12 months prior to time of screening. History of CAD determined by documentation of percutaneous coronary intervention or coronary artery bypass surgery within the last 1-12 months.
  3. Able to complete a survey independently
  4. Access to a phone
  5. Willingness to participate as evidenced by signing of the study informed consent form

Exclusion Criteria:

  1. Inability to speak, read and write in English
  2. Cognitive impairment
  3. Severe physical or mental illness
  4. Limited life expectancy (projected to be less than 1 year)

Sites / Locations

  • Peter Munk Cardiac Centre - University Health NetworkRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

ACE Screen

Lifestyle Assessment

Arm Description

At the initial visit, the Philadelphia ACE Survey, a validated ACE questionnaire, will be administered by a research coordinator. A Lifestyle Assessment package will also be provided for self-completion, featuring General Demographics, Cardiovascular and Medication History, Health Behaviours, the Short Form (36) Health Survey, the Patient Health Questionnaire-9, the General Anxiety Disorder-7 questionnaire, the Seattle Angina Questionnaire-7, and the modified Perceived Need for Card Questionnaire. Patients who test positive for ACE will receive a 3-page printed ACE Resource Pack. At 3 months, the Lifestyle Assessment will be administered again. At 6 months, the Philadelphia ACE survey, Lifestyle Assessment, as well as a scale assessing their comfort level in being screened for ACE, disclosing their ACE status to their clinicians, and their confidence level in their clinicians' ability to help them manage their ACEs will be administered.

At the initial visit, no Philadelphia ACE Survey will be administered. The Lifestyle Assessment packaged will be provided for self-completion, featuring General Demographics, Cardiovascular and Medication History, Health Behaviours, the Short Form (36) Health Survey, the Patient Health Questionnaire-9, the General Anxiety Disorder-7 questionnaire, the Seattle Angina Questionnaire-7, and the modified Perceived Need for Card Questionnaire. At 3 months, the Lifestyle Assessment will be administered again. At 6 months, the Philadelphia ACE survey, Lifestyle Assessment, as well as a scale assessing their comfort level in being screened for ACE, disclosing their ACE status to their clinicians, and their confidence level in their clinicians' ability to help them manage their ACEs will be administered.

Outcomes

Primary Outcome Measures

Patient-reported quality of life
Degree of change in quality of life measured by the Short Form (36) Health Survey questionnaire

Secondary Outcome Measures

Mortality
Rate of all-cause mortality
Cardiovascular hospitalization
Rate of hospitalization for ACS, heart failure, stroke and atrial fibrillation
Myocardial infarction
Rate of myocardial infarction
Stroke
Rate of stroke
Need for urgent repeat coronary revascularization
Rate of need for urgent repeat coronary revascularization

Full Information

First Posted
February 9, 2021
Last Updated
May 27, 2022
Sponsor
University Health Network, Toronto
Collaborators
Socar Research SA
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1. Study Identification

Unique Protocol Identification Number
NCT04752228
Brief Title
Adverse Childhood Experiences in Patients With Coronary Artery Disease Pilot
Official Title
Adverse Childhood Experiences in Patients With Coronary Artery Disease: a Pilot Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Health Network, Toronto
Collaborators
Socar Research SA

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Adverse Childhood Experiences (ACEs) are potentially harmful events occurring during childhood that have been associated with chronic physical conditions in adulthood, including coronary artery disease (CAD). ACEs may constitute a portion of the remaining unexplained residual risk for CAD in adults. Identifying a means of addressing these experiences may mitigate their health consequences and result in improved cardiovascular outcomes. The primary objective of this study is to determine if patients who undergo ACE screening experience improved quality of life compared to patients who undergo conventional lifestyle assessment. This will be a single-centre, pragmatic, single-blinded (i.e. data analysts), 1:1, pilot randomized control trial.
Detailed Description
ACEs encapsulate a broad spectrum of traumatic and distressing events occurring before the age of 18 that span the domains of abuse, household dysfunction, neglect, amongst others, and that threaten a child's physical, familial or social safety. The landmark ACE Study, published by Felitti and colleagues, was the first study to propose the association between ACEs and the development of chronic physical conditions in adulthood, including cardiovascular disease (CVD). Due to a variety of mechanisms, exposure to an ACE increases predisposition to the development of CVD and its conventional risk factors. ACEs nonetheless remain underrecognized and undermanaged in routine cardiovascular clinical encounters. Integration of ACE screening into the standardized clinical assessment of CVD may enable cardiologists to better identify patients who might benefit from further post-ACE resiliency interventions and serve as an impactful secondary and tertiary prevention strategy. The ACE screening process itself may be therapeutic as it gives patients the opportunity to discuss their early experiences, reflect on the role of early adversity in their current health problems, and have some sympathetic acknowledgement about this history from a health care professional. This has been termed "ACE insight". Screening for ACEs has been found to be acceptable by patients. Patients may have never had any opportunity to discuss ACEs they have undergone throughout their entire life, enabling their effects to propagate into adulthood. Inquiring about ACE exposure during clinical encounters with all patients may garner insights that can have a beneficial effect in improving cardiovascular health. Additionally, engaging patients in stress-coping therapies, such as mindfulness, and referral for psychological consultation as needed, may also be helpful. Although logical, these strategies still lack adequate evidence and a randomized trial is needed to evaluate their potential in reducing the occurrence of cardiovascular events. This study aims to assess whether deleterious childhood exposures are associated with an increased prevalence of risk factors for CAD and represent an independent risk factor for CAD. Furthermore, screening for ACEs in patients with CAD may serve as a therapeutic intervention in itself by providing both ACE insight and a platform to unload internal psychological burdens. Screening may result in an enhanced quality of life, as well as improved health behaviours that may benefit their cardiovascular outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adverse Childhood Experiences, Coronary Artery Disease

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ACE Screen
Arm Type
Experimental
Arm Description
At the initial visit, the Philadelphia ACE Survey, a validated ACE questionnaire, will be administered by a research coordinator. A Lifestyle Assessment package will also be provided for self-completion, featuring General Demographics, Cardiovascular and Medication History, Health Behaviours, the Short Form (36) Health Survey, the Patient Health Questionnaire-9, the General Anxiety Disorder-7 questionnaire, the Seattle Angina Questionnaire-7, and the modified Perceived Need for Card Questionnaire. Patients who test positive for ACE will receive a 3-page printed ACE Resource Pack. At 3 months, the Lifestyle Assessment will be administered again. At 6 months, the Philadelphia ACE survey, Lifestyle Assessment, as well as a scale assessing their comfort level in being screened for ACE, disclosing their ACE status to their clinicians, and their confidence level in their clinicians' ability to help them manage their ACEs will be administered.
Arm Title
Lifestyle Assessment
Arm Type
Other
Arm Description
At the initial visit, no Philadelphia ACE Survey will be administered. The Lifestyle Assessment packaged will be provided for self-completion, featuring General Demographics, Cardiovascular and Medication History, Health Behaviours, the Short Form (36) Health Survey, the Patient Health Questionnaire-9, the General Anxiety Disorder-7 questionnaire, the Seattle Angina Questionnaire-7, and the modified Perceived Need for Card Questionnaire. At 3 months, the Lifestyle Assessment will be administered again. At 6 months, the Philadelphia ACE survey, Lifestyle Assessment, as well as a scale assessing their comfort level in being screened for ACE, disclosing their ACE status to their clinicians, and their confidence level in their clinicians' ability to help them manage their ACEs will be administered.
Intervention Type
Other
Intervention Name(s)
Philadelphia ACE Survey
Intervention Description
The Philadelphia ACE survey assesses the three major domains featured within the original ACE Study Questionnaire developed by Felitti et al. (abuse, neglect, and family dysfunction), in addition to five community-level stressors.
Intervention Type
Other
Intervention Name(s)
Lifestyle Assessment
Intervention Description
The Lifestyle Assessment questionnaire features the Short Form (36) Health Survey, Patient Health Questionnaire-9, General Anxiety Disorder-7 questionnaire, Seattle Angina Questionnaire-7, and modified Perceived Need for Card Questionnaire, which are validated questionnaires for the assessment of quality of life, depression, anxiety, angina, and perceived need for care, respectively.
Primary Outcome Measure Information:
Title
Patient-reported quality of life
Description
Degree of change in quality of life measured by the Short Form (36) Health Survey questionnaire
Time Frame
3 and 6 months
Secondary Outcome Measure Information:
Title
Mortality
Description
Rate of all-cause mortality
Time Frame
6 months
Title
Cardiovascular hospitalization
Description
Rate of hospitalization for ACS, heart failure, stroke and atrial fibrillation
Time Frame
6 months
Title
Myocardial infarction
Description
Rate of myocardial infarction
Time Frame
6 months
Title
Stroke
Description
Rate of stroke
Time Frame
6 months
Title
Need for urgent repeat coronary revascularization
Description
Rate of need for urgent repeat coronary revascularization
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Health behaviour
Description
Change in health behaviours, measured using constructs derived from the American Heart Association
Time Frame
3 and 6 months
Title
Depression
Description
Change in severity of depression, measured using the Patient Health Questionnaire 9
Time Frame
3 and 6 months
Title
Anxiety
Description
Change in severity of anxiety, measured using the Generalized Anxiety Disorder-7 scale
Time Frame
3 and 6 months
Title
Angina
Description
Change in angina, measured by the Seattle Angina Questionnaire
Time Frame
3 and 6 months
Title
Perceived need for care
Description
Change in perceived need for care, measured by the Modified Perceived Need for Care Questionnaire
Time Frame
3 and 6 months
Title
Prevalence of ACE
Description
Percentage of patients with CAD who report history of ACE
Time Frame
0 and 6 months
Title
Patient preferences on ACE screening
Description
Scale assessing comfort level in being screened for ACE, disclosing their ACE status to their clinicians, and their confidence level in their clinicians' ability to help them manage their ACEs
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years at screening History of (1) acute coronary syndrome (ACS) OR (2) coronary artery disease (CAD) necessitating prior cardiovascular intervention. History of ACS determined by documentation of ST-elevation myocardial infarction or non-ST-segment elevation infarction 1-12 months prior to time of screening. History of CAD determined by documentation of percutaneous coronary intervention or coronary artery bypass surgery within the last 1-12 months. Able to complete a survey independently Access to a phone Willingness to participate as evidenced by signing of the study informed consent form Exclusion Criteria: Inability to speak, read and write in English Cognitive impairment Severe physical or mental illness Limited life expectancy (projected to be less than 1 year)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Farkouh, MD
Phone
416-340-3141
Email
michael.farkouh@uhn.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Amanda Garrioch
Phone
416-340-4800
Ext
2746
Email
amanda.garrioch@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Farkouh, MD
Organizational Affiliation
University Health Network-Toronto General Hospital, Canada
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claudia Frankfurter, MD
Organizational Affiliation
University Health Network-Toronto General Hospital, Canada
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lucas C Godoy, MD
Organizational Affiliation
University Health Network-Toronto General Hospital, Canada
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christine Lay, MD
Organizational Affiliation
Women's College Hospital, Canada
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert Maunder, MD
Organizational Affiliation
Mount Sinai Hospital, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peter Munk Cardiac Centre - University Health Network
City
Toronto
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amanda Garrioch
Phone
416-340-4800
Ext
2746
Email
amanda.garrioch@uhn.ca

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
9635069
Citation
Felitti VJ, Anda RF, Nordenberg D, Williamson DF, Spitz AM, Edwards V, Koss MP, Marks JS. Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. Am J Prev Med. 1998 May;14(4):245-58. doi: 10.1016/s0749-3797(98)00017-8.
Results Reference
background
PubMed Identifier
33263716
Citation
Godoy LC, Frankfurter C, Cooper M, Lay C, Maunder R, Farkouh ME. Association of Adverse Childhood Experiences With Cardiovascular Disease Later in Life: A Review. JAMA Cardiol. 2021 Feb 1;6(2):228-235. doi: 10.1001/jamacardio.2020.6050.
Results Reference
background
PubMed Identifier
32293444
Citation
Maunder RG, Hunter JJ, Tannenbaum DW, Le TL, Lay C. Physicians' knowledge and practices regarding screening adult patients for adverse childhood experiences: a survey. BMC Health Serv Res. 2020 Apr 15;20(1):314. doi: 10.1186/s12913-020-05124-6.
Results Reference
background
PubMed Identifier
31881981
Citation
Maunder RG, Tannenbaum DW, Permaul JA, Nutik M, Haber C, Mitri M, Costantini D, Hunter JJ. The prevalence and clinical correlates of adverse childhood experiences in a cross-sectional study of primary care patients with cardiometabolic disease or risk factors. BMC Cardiovasc Disord. 2019 Dec 19;19(1):304. doi: 10.1186/s12872-019-01277-3.
Results Reference
background

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Adverse Childhood Experiences in Patients With Coronary Artery Disease Pilot

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