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Interventions to Support Long-Term Adherence aNd Decrease Cardiovascular Events Post-Myocardial Infarction (ISLAND)

Primary Purpose

Myocardial Infarction, Coronary Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Usual care + letters
Usual care + letters + automated calls
Sponsored by
Women's College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Myocardial Infarction

Eligibility Criteria

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

Inclusion Criteria:

  • Patients aged 18 years and older having a coronary angiography following a myocardial infarction (ST-elevation myocardial infarction or non-ST-elevation myocardial infarction), with evidence of coronary artery disease (>50% blockage of left main or >70% blockage of ≥1 major cardiac arteries).
  • Discharged from the catheterization centre alive, either home or to a local (non-cardiac) hospital
  • Patients must be Ontario residents

Exclusion Criteria:

  • Patients will be excluded if they expire during their hospitalization or if they have cardiogenic shock (Killip Class 4) at the time of their post-MI coronary angiography due to their poor prognosis.(El-Menyar et al., 2012)
  • Patients will also be excluded if they require a translator to receive services in English as recorded in the CCN referral form, as it is infeasible to offer the interventions in multiple languages at this stage.
  • Patients whose data are not complete and received in time to deliver the first post-procedure intervention will be excluded as they cannot receive the intervention as intended.
  • Patients who do not have an Ontario health card number

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    No Intervention

    Experimental

    Experimental

    Arm Label

    Usual care

    Usual care + letters

    Usual care + letters + automated calls

    Arm Description

    Usual care (no intervention)

    Usual care plus a series of postal educational reminders (including information for patients to share with clinicians)

    Usual care plus a series of postal educational reminders (including information for patients to share with clinicians), plus automated reminder interactive voice response phone calls to identify patients at being at risk for non-adherence and a trained lay health worker to provide additional support and navigation for such patients via telephone.

    Outcomes

    Primary Outcome Measures

    Medication adherence
    Number of cardiac medication classes with no missed tablets in last week (ordinal) [patient report]
    Cardiac rehabilitation completion
    Patient attended at least one of the rehabilitation components and formal re-assessment at the conclusion of the program (dichotomous) [patient report]

    Secondary Outcome Measures

    Cardiac rehabilitation attendance
    Participation, defined as attending at least one exercise session following enrolment assessment (dichotomous) [patient report]
    Quality of life
    Seattle Angina Questionnaire-7 [patient report]
    Treatment discussion
    Adherence to both medication and exercise discussed with providers in last three months (dichotomous) [patient report]
    Smoking status
    Point-prevalence, smoking any cigarettes in last three months (dichotomous) [patient report]
    Medication persistence
    Active prescription for ALL recommended medications (dichotomous) [patient report]
    Medication persistence
    Active prescription for EACH recommended medication (dichotomous) [patient report]
    Medication adherence
    No missed tablets in last week for ANY recommended medication (dichotomous) [patient report]
    Medication adherence
    No missed tablets in last month for any recommended medication (dichotomous)[patient report]
    Medication adherence
    No missed tablets in last month for ANY recommended medication (dichotomous) [patient report]
    Medication adherence
    Number of missed tablets in last week for EACH recommended medication (continuous, 0 to 28) [patient report]
    Medication adherence
    Number of missed tablets in last month for each recommended medication (continuous, 0 to 28) [patient report]
    Medication adherence
    Medication possession ratio > 80% for ALL recommended medications in those 65+ (dichotomous) [administrative data]
    Medication adherence
    Medication possession ratio > 80% for EACH of the recommended medications in those 65+ (dichotomous) [administrative data]
    Medication adherence
    Mean medication possession ratio for ALL recommended medications in those 65+ (continuous, 0 to 100) [administrative data]
    Medication adherence
    Mean medication possession ratio for EACH recommended medication in those 65+ (continuous, 0 to 100) [administrative data]
    Cardiovascular event
    Coronary bypass surgery or stent or repeat MI (dichotomous) [administrative data]
    Mortality
    Death during follow-up [administrative data]
    Health utilization
    Outpatient visits (count) [administrative data]
    Health utilization
    Emergency Room visits not leading to admission (count) [administrative data]
    Health utilization
    Hospitalizations (count) [administrative data]

    Full Information

    First Posted
    March 2, 2015
    Last Updated
    March 22, 2018
    Sponsor
    Women's College Hospital
    Collaborators
    Population Health Research Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02382731
    Brief Title
    Interventions to Support Long-Term Adherence aNd Decrease Cardiovascular Events Post-Myocardial Infarction
    Acronym
    ISLAND
    Official Title
    Interventions to Support Long-Term Adherence aNd Decrease Cardiovascular Events Post-Myocardial Infarction
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2015 (undefined)
    Primary Completion Date
    June 2017 (Actual)
    Study Completion Date
    October 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Women's College Hospital
    Collaborators
    Population Health Research Institute

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Proven treatments exist that improve quality of life and reduce the risk of repeat heart attacks or death amongst persons who have already had one heart attack. These treatments include medications and supervised cardiac rehabilitation programs. Unfortunately, research shows that many people who have had a heart attack do not stick with these treatments and therefore cannot benefit. This quality improvement research program seeks to understand the impact of interventions that could be readily implemented at scale by entire health systems or organizations wishing to improve adherence to proven treatments. Specifically, the trial will test whether providing Ontario-based patients (and their health professionals) with repeated educational reminders delivered via post and phone will help improve the use of medications or attendance at cardiac rehabilitation. During the project, the types of patients who are most responsive will be identified as will the most cost-effective strategy for delivering reminders. The trial team are partnering in this project with health system decision makers who have an interest in using the results to create standard operating procedures that could benefit patients across the province.
    Detailed Description
    EXECUTIVE SUMMARY Background: In patients who have had a myocardial infarction (MI) and coronary disease, guidelines recommend cardiac rehabilitation services and the long-term use of cardiac medications to reduce the risk of recurrent cardiovascular events. Adherence to these recommendations substantially reduces morbidity and mortality post-MI. However, for a variety of patient, provider, and system-level reasons, adherence to cardiac medications declines to approximately 50% by 12 months. Likewise, only 30-40% of patients participate in cardiac rehabilitation. Thus, interventions to increase secondary prevention treatment adherence are urgently needed. The Cardiac Care Network of Ontario (CCN) holds a registry of all patients in the province who have a coronary angiography. The registry has been used to identify gaps in care and to plan health system strategies for high-risk patients. More recently, a pilot trial was conducted in Hamilton by the trial team using data in the registry to send recurrent postal reminders regarding the importance of treatment adherence to patients, their pharmacists, and family physicians. A similar program is underway in Ottawa using automated phone calls with interactive voice response and nurse follow up. These interventions both have the potential to address known determinants of adherence. The CCN, Ministry of Health and Long-Term Care, Health Quality Ontario, and other stakeholders across Ontario are interested in evaluating the comparative effectiveness and costs of these interventions. Research Questions: The research objectives were formed by the decision makers' need to evaluate whether and in what format to sustain and/or scale-up post-MI educational reminder interventions: i. Can educational reminders delivered via post and/or using interactive voice response with personalized telephone follow up improve secondary prevention treatment adherence post-MI? ii. How do different approaches to improve adherence to these recommendations compare in terms of clinical effectiveness and costs? iii. Which subgroups are more/less likely to respond to reminders? Research Approach: This is a pragmatic, randomized controlled trial with blinded outcome assessment. Patients in cardiac centres throughout Ontario who undergo a coronary angiography will be provided a letter of information explaining the study appended to the standard CCN letter of information. CCN will identify eligible patients (those with substantial coronary artery disease who survive their initial hospitalization post-MI) and provide the patient list back to the cardiac centre. A representative at the centre will securely send this list to the Population Health Research Institute in Hamilton. Patients will be randomized by the Population Health Research Institute team to one of three arms: - Usual care, with no standardized educational materials or reminders - Postal letters sent from Population Health Research Institute on behalf of each hospital's interventional cardiology team to the patient approximately 4, 8, 20, 32, and 44 weeks post-MI, with an insert for the family physician and pharmacist at approximately 4 and 8 weeks post-MI. - Postal letters as above plus interactive voice response phone calls to the patient delivered approximately 2 weeks after the letters, as well as personalized telephone follow up by trained lay health workers for patients identified by the interactive voice response system as non-adherent. Patient self-report and administrative data will be used to assess outcomes 12 months post-MI. Analyses will be by intention to treat. The primary outcome is adherence to guideline-recommended treatments. Secondary outcomes include health services utilization (including outpatient visits to interventional cardiology), recurrent cardiovascular events, and mortality. During the trial, a theory-informed process questionnaire will be administered to a random sub-sample. An economic evaluation will be conducted from the perspective of the public health care payer. Implications: This project has the potential to lead to improvements in care for patients at high cardiovascular risk as well as provide generalizable insights regarding how to optimize interventions to improve adherence. Further, it has the potential to inform how other health databases could be used to improve health system performance.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Myocardial Infarction, Coronary Disease

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    2742 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Usual care
    Arm Type
    No Intervention
    Arm Description
    Usual care (no intervention)
    Arm Title
    Usual care + letters
    Arm Type
    Experimental
    Arm Description
    Usual care plus a series of postal educational reminders (including information for patients to share with clinicians)
    Arm Title
    Usual care + letters + automated calls
    Arm Type
    Experimental
    Arm Description
    Usual care plus a series of postal educational reminders (including information for patients to share with clinicians), plus automated reminder interactive voice response phone calls to identify patients at being at risk for non-adherence and a trained lay health worker to provide additional support and navigation for such patients via telephone.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Usual care + letters
    Intervention Description
    A series of five postal educational reminders sent on behalf of each hospital's interventional cardiology team to the patient approximately 4, 8, 20, 32, and 44 weeks post-MI procedure, with an insert for the family physician and pharmacist at approximately 4 and 8 weeks post-MI procedure.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Usual care + letters + automated calls
    Intervention Description
    A series of five postal educational reminders as per the usual care + letters arm plus interactive voice response phone calls to the patient delivered approximately 2 weeks after the letters, as well as personalized telephone follow up by trained lay health workers for patients identified by the interactive voice response system as non-adherent. The automated algorithm is designed to identify patients who are non-adherent and who may benefit from personalized educational phone call and/or system navigation support by the lay health worker. Lay health workers will not provide clinical advice.
    Primary Outcome Measure Information:
    Title
    Medication adherence
    Description
    Number of cardiac medication classes with no missed tablets in last week (ordinal) [patient report]
    Time Frame
    12 months post-MI
    Title
    Cardiac rehabilitation completion
    Description
    Patient attended at least one of the rehabilitation components and formal re-assessment at the conclusion of the program (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Secondary Outcome Measure Information:
    Title
    Cardiac rehabilitation attendance
    Description
    Participation, defined as attending at least one exercise session following enrolment assessment (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Quality of life
    Description
    Seattle Angina Questionnaire-7 [patient report]
    Time Frame
    12 months post-MI
    Title
    Treatment discussion
    Description
    Adherence to both medication and exercise discussed with providers in last three months (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Smoking status
    Description
    Point-prevalence, smoking any cigarettes in last three months (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication persistence
    Description
    Active prescription for ALL recommended medications (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication persistence
    Description
    Active prescription for EACH recommended medication (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    No missed tablets in last week for ANY recommended medication (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    No missed tablets in last month for any recommended medication (dichotomous)[patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    No missed tablets in last month for ANY recommended medication (dichotomous) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Number of missed tablets in last week for EACH recommended medication (continuous, 0 to 28) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Number of missed tablets in last month for each recommended medication (continuous, 0 to 28) [patient report]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Medication possession ratio > 80% for ALL recommended medications in those 65+ (dichotomous) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Medication possession ratio > 80% for EACH of the recommended medications in those 65+ (dichotomous) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Mean medication possession ratio for ALL recommended medications in those 65+ (continuous, 0 to 100) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Medication adherence
    Description
    Mean medication possession ratio for EACH recommended medication in those 65+ (continuous, 0 to 100) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Cardiovascular event
    Description
    Coronary bypass surgery or stent or repeat MI (dichotomous) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Mortality
    Description
    Death during follow-up [administrative data]
    Time Frame
    12 months post-MI
    Title
    Health utilization
    Description
    Outpatient visits (count) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Health utilization
    Description
    Emergency Room visits not leading to admission (count) [administrative data]
    Time Frame
    12 months post-MI
    Title
    Health utilization
    Description
    Hospitalizations (count) [administrative data]
    Time Frame
    12 months post-MI

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients aged 18 years and older having a coronary angiography following a myocardial infarction (ST-elevation myocardial infarction or non-ST-elevation myocardial infarction), with evidence of coronary artery disease (>50% blockage of left main or >70% blockage of ≥1 major cardiac arteries). Discharged from the catheterization centre alive, either home or to a local (non-cardiac) hospital Patients must be Ontario residents Exclusion Criteria: Patients will be excluded if they expire during their hospitalization or if they have cardiogenic shock (Killip Class 4) at the time of their post-MI coronary angiography due to their poor prognosis.(El-Menyar et al., 2012) Patients will also be excluded if they require a translator to receive services in English as recorded in the CCN referral form, as it is infeasible to offer the interventions in multiple languages at this stage. Patients whose data are not complete and received in time to deliver the first post-procedure intervention will be excluded as they cannot receive the intervention as intended. Patients who do not have an Ontario health card number
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Noah Ivers
    Organizational Affiliation
    Women's College Hospital
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    John-David Schwalm
    Organizational Affiliation
    Population Health Research Institute
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Madhu Natarajan
    Organizational Affiliation
    Population Health Research Institute
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jeremy Grimshaw
    Organizational Affiliation
    Ottawa Hospital Research Institute
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    21159479
    Citation
    El-Menyar A, Zubaid M, AlMahmeed W, Sulaiman K, AlNabti A, Singh R, Al Suwaidi J. Killip classification in patients with acute coronary syndrome: insight from a multicenter registry. Am J Emerg Med. 2012 Jan;30(1):97-103. doi: 10.1016/j.ajem.2010.10.011. Epub 2010 Dec 14.
    Results Reference
    background
    PubMed Identifier
    35596020
    Citation
    McCleary N, Ivers NM, Schwalm JD, Witteman HO, Taljaard M, Desveaux L, Bouck Z, Grace SL, Grimshaw JM, Presseau J. Impacts of two behavior change interventions on determinants of medication adherence: process evaluation applying the health action process approach and habit theory alongside a randomized controlled trial. J Behav Med. 2022 Oct;45(5):659-673. doi: 10.1007/s10865-022-00327-0. Epub 2022 May 20.
    Results Reference
    derived
    PubMed Identifier
    32883724
    Citation
    Desveaux L, Saragosa M, Russell K, McCleary N, Presseau J, Witteman HO, Schwalm JD, Ivers NM. How and why a multifaceted intervention to improve adherence post-MI worked for some (and could work better for others): an outcome-driven qualitative process evaluation. BMJ Open. 2020 Sep 3;10(9):e036750. doi: 10.1136/bmjopen-2019-036750.
    Results Reference
    derived
    PubMed Identifier
    32522811
    Citation
    Ivers NM, Schwalm JD, Bouck Z, McCready T, Taljaard M, Grace SL, Cunningham J, Bosiak B, Presseau J, Witteman HO, Suskin N, Wijeysundera HC, Atzema C, Bhatia RS, Natarajan M, Grimshaw JM. Interventions supporting long term adherence and decreasing cardiovascular events after myocardial infarction (ISLAND): pragmatic randomised controlled trial. BMJ. 2020 Jun 10;369:m1731. doi: 10.1136/bmj.m1731.
    Results Reference
    derived

    Learn more about this trial

    Interventions to Support Long-Term Adherence aNd Decrease Cardiovascular Events Post-Myocardial Infarction

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