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
About this trial
This is an interventional health services research trial for Myocardial Infarction
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
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
NCT ID
NCT02382731
First Posted
March 2, 2015
Last Updated
March 22, 2018
Sponsor
Women's College Hospital
Collaborators
Population Health Research Institute
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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