Acute Myocardial Infarction - Allied Health-Oriented Patient-centered Digitally-Enabled Care
AMI-HOPE
1 other identifier
interventional
1,633
1 country
6
Brief Summary
The Acute Myocardial Infarction - allied Health Oriented, Patient centered, and digitally Enabled care (AMI-HOPE) program is a model of care designed to improve post-AMI well-being, safety, and outcomes through greater involvement of AHPs in patient care and integrating digital technologies into routine primary care disease management. AMI-HOPE aims to deliver solutions to these identified gaps of care which will transform healthcare planning both at cluster and national levels. The cornerstone of the AMI-HOPE program will be upskilling pharmacists to take on low-intermediate complexity clinician roles during the post-discharge period. The first 6 months will be anchored by tertiary care before a handoff to primary care. This frees up cardiologists to focus on high complexity cases.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2023
Longer than P75 for not_applicable
6 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 11, 2023
CompletedFirst Submitted
Initial submission to the registry
February 1, 2026
CompletedFirst Posted
Study publicly available on registry
March 2, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
March 2, 2026
February 1, 2026
3.7 years
February 1, 2026
February 25, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Death and Unplanned Cardiovascular Disease (CVD) related (non-fatal MI, non-fatal stroke, others) rehospitalizations
Counts and time to any events of death or unplanned CVD related rehospitalizations
between enrolment and end of 12-month follow up
Secondary Outcomes (11)
Absolute change in concentration of Low-Density Lipoprotein Cholesterol (LDL-C)
between enrolment and end of 12-month follow up
Change in Blood Pressure (BP)
At discharge, 2 week, 1, 3, 6, 9 &12 months
Change in Haemoglobin A1c (HbA1c)
between enrolment and end of 12-month follow up
EuroQoL (Quality of Life)-5 Dimensions (EQ-5D) Scores in Participants
At 1 month and 12 month
Patient Activation Measure (PAM-13) Scores in Participants
At discharge and 6month
- +6 more secondary outcomes
Other Outcomes (1)
Cost-effectiveness
At the end of 12-month follow up
Study Arms (2)
Control
OTHERStandard of Care
Pharmacist-led digital platform assisted care
OTHERAMI-HOPE centers around a digital platform that offers continuous telemonitoring on patients' vitals, tailored medication prescription with support from pharmacists, and personalised lifestyle nudges and educational material.
Interventions
Standard of care treatment without the pharmacist-led digital platform assisted care
Up titration of medications by pharmacist. AMI-HOPE centers around a digital platform that offers continuous telemonitoring on patients' vitals, tailored medication prescription with support from pharmacists and personalised lifestyle nudges and educational material.
Eligibility Criteria
You may qualify if:
- Male or Female, aged 21 to 90 years (inclusive), at the time of signing the informed consent form
- Clinically diagnosed with AMI during index hospitalisation
- Own a mobile phone with internet access- intervention arm only
You may not qualify if:
- Patients who are planned for palliative care or life expectancy \<1 year
- Foreigners who do not have Singaporean citizenship/ Permanent Resident (PR) status
- Patients who are enrolled into Healthier SG affiliated with General Practitioners (GPs)
- Allergy or intolerance of Angiotensin-Converting Enzyme Inhibitors (ACE-I) or Angiotensin II Receptor Blockers (ARB)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (6)
Changi General Hospital (CGH)
Singapore, Singapore
Khoo Teck Puat Hospital (KTPH)
Singapore, Singapore
National Heart Centre Singapore (NHCS)
Singapore, Singapore
National University Heart Centre, Singapore (NUHCS)
Singapore, Singapore
Ng Teng Fong General Hospital (NTFGH)
Singapore, Singapore
Tan Tock Seng Hospital (TTSH)
Singapore, Singapore
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mark Chan
National University Heart Centre, Singapore
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Deputy Executive Director and Senior Consultant, National University Heart Centre
Study Record Dates
First Submitted
February 1, 2026
First Posted
March 2, 2026
Study Start
January 11, 2023
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
March 2, 2026
Record last verified: 2026-02