VICTORION-ASCERTAIN: Implementation Study (v-ASCERTAIN) (v-ASCERTAIN)

AtheroSclerotic Cardiovascular disEase Risk assessmenT and treAtment In AustraliaN Primary Care (VICTORION-ASCERTAIN: Implementation Study)

The goal of this study is to understand and compare an alternative model of care in comparison to the usual model of care in include male and female participants ≥18 years of age with a history of ASCVD (hear and blood vessels diseases) or high-risk participants who have elevated bad cholesterol (LDL-C ≥1.8 mmol/L). The alternative model of care includes telephone support calls from a study nurse (after visits 1,2 and 4) and text messages to your mobile phone with healthy heart information.

The main question it aims to answer is to understand and compare an alternative model of care in comparison to the usual model of care by evaluating the study participants bad cholesterol values after 180 and 365 days of the study.

Each participant will take their medications as per usual care but may have the addition of Inclisiran, 284 mg 1.5 ml liquid in a single-use prefilled syringe for under skin administration. In accordance with the current medical practice guidelines for treating heart related conditions, Inclisiran and its product information will be made available for use in both care models.

All the participants who decide to take part in this study will be requested to do the following:

• Answer any questions from the study doctor or the study staff as accurately as possible when asked about changes in health status, medications, heart health, visits to other doctors or hospital admissions, planned surgery, even if they think none of these are related to the study.
• Study doctor will be able to inform them of which medications you can and cannot take as part of this study.
• To use mobile phone to receive text messages and/or questionnaires as proposed in the new model of care.
• Advise the study doctor if they plan to move away from the geographical area where the study is being conducted during the study period.
• Take the medications for cholesterol lowering treatment (such as a statin and/or ezetimibe) that are prescribed by the study doctor.
• Tell the study doctor or study staff as soon as possible about suspected participant / participant partner pregnancy.
• Tell the study doctor or study staff if they change their mind about taking part in the study.
• Attend all the visits (screening visit, visits 1, 2, 3, 4 and visit 5).
• Provide all the information that will enable the study team to contact them, i.e., inform the study staff if contact details change, provide contact details of a family member, etc.

Study Overview

• Status: Recruiting
• Conditions: Cerebrovascular Disease; Coronary Heart Disease (CHD); Peripheral Arterial Disease (PAD); Atherosclerotic Cardiovascular Disease (ASCVD)
• Intervention / Treatment: Drug: Inclisiran Prefilled Syringe; Other: SMS messages; Other: Telephone-based support calls

Detailed Description

ASCVD remains a significant burden in the Australian population. Moreover, based on recent local data, it is clear that there are still opportunities to improve the management of this condition in Australia.

In collaboration with leading experts in the field, analysis of the gaps in management of cholesterol in Australia has been undertaken. Key areas identified include Lack of regular lipid testing in general practice, Limited access to full range of management tools, current therapies aren't achieving clinical guidelines and poor medication adherence.

To address these pain points, the ASCERTAIN study will implement a new model of care that has been co-created with leading cardiologists in Australia and feedback has been provided by a General Practitioner (GP) Advisory Committee.

As the primary purpose of this study is to assess the impact of a new model of care compared to usual care, Inclisiran and its approved Product Information will be made available in both arms to be used as per the treating physician's discretion. Participants taking part in this study will receive maximally tolerated statin and/or ezetimibe therapy with or without other LDL-C lowering therapies as per the treating physician's discretion.

The primary clinical question of interest is:

What is the effectiveness of a new model of care implementation strategy compared to usual care in patients who have not reached their LDL-target?

In the usual care arm:

1- The GPs will be educated on the European Society of Cardiology (ESC) guidelines and Guideline Directed Management therapy (GDMT)

In the new model of care arm:

1. The GPs will be educated on the ESC guidelines and Guideline Directed Management therapy (GDMT).
2. The Participants enrolled in this arm will be receiving monthly short message service (SMS) messages with regards to regarding cardiovascular health and appointment reminders (low touch engagement nudges).
3. In addition, Participants will receive telephone-based support calls from a study nurse trained in motivational interviewing. These telephone calls will cover diet, exercise, medication, and where necessary smoking cessation. A summary of any recommendations will then be sent to the primary care physician via email or letter. However, ultimately the primary care physician is responsible for the management of their patient.

The study will include male and female participants ≥18 years of age with a history of ASCVD (coronary heart disease, ischaemic cerebrovascular disease or peripheral arterial disease) or ASCVD-risk equivalents who have elevated LDL-C (≥1.8 mmol/L). A total of approximately 600 participants will be included in the study and will be randomised in a 1:1 ratio at approximately 20 sites across Australia.

For the purposes of defining the ASCVD-risk equivalent group, the Guidelines for the Management of Absolute Cardiovascular Disease Risk (2023) in Australian adults will be used. As per these guidelines, the online calculator www.cvdcheck.org.au (which is based on the Framingham Risk Equation) will be used to calculate an individual's estimated 5-year absolute CVD risk. High risk corresponds to >10% probability of CVD within the next 5 years.

As this study will utilise Electronic Health Records (EHR), only clinics using Medical Director (MD) Clinical software will be able to participate in this study. Potential sites may be identified by running a search of the practice databases. From a recruitment and practicality perspective, in the first instance, those clinics that have a high volume of potential patients who meet the eligibility criteria will be considered. Additional formal feasibility assessment will be completed by the Sponsor to ensure clinics are suitable for participation in the study.

Study sites may receive a list of patients who could qualify for the study. This list will be generated by a search of the practice database running a query for patients that satisfy the inclusion criteria. Alternatively, the sites may identify patients who could qualify for the study independently. The study sites will contact participants who meet the eligibility criteria.

Patient Reported Outcomes (PROs) will be completed by the participant electronically. Participants will receive a link to the questionnaire via text message or email.

The analysis will be performed at the end of the study, after the data for all participants are available. Unless otherwise specified, all statistical tests will be conducted against a two-sided alternative hypothesis, employing a significance level of 0.05.

Efficacy, safety, and other data will be summarised. For continuous variables, summary statistics (mean, standard deviation, median, interquartile range, minimum, and maximum) at each time point and for change from baseline to each time point will be reported by study arm. For discrete variables, frequency counts and percentages at each time point will be reported by study arm.

• Study Type: Interventional
• Enrollment (Estimated): 600
• Phase: Phase 4

Contacts and Locations

• Study Contact: Name: Julie Butters; Phone Number: +61 434679018; Email: julie.butters@monash.edu

Study Locations

• Australia
  • South Australia
    • Adelaide, South Australia, Australia, 5044
      • Recruiting
      • Somerton Park Day & Night Medical Centre
      • Principal Investigator: Stephen Nicholls, MBBS
      • Contact: Domenic Sacca; Phone Number: 0423245187; Email: domenic.sacca@monash.edu

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Study Population

The study will include male and female participants ≥18 years of age with a history of ASCVD (coronary heart disease, ischaemic cerebrovascular disease or peripheral arterial disease) or ASCVD-risk equivalents who have elevated LDL-C (≥1.8 mmol/L). A total of approximately 600 participants will be included in the study across approximately 20 sites.

Description

Inclusion Criteria:

1. Signed informed consent must be obtained prior to participation in the study
2. Males and females ≥18 years of age

3. Documented History of ASCVD

   a. Coronary heart disease (CHD):

   1. Prior myocardial infarction
   2. Prior coronary revascularisation (PCI or CABG)

   b. Cerebrovascular disease:

   1. Prior documented ischaemic stroke
   2. Documented Carotid artery stenosis >70%
   3. History of prior percutaneous or surgical carotid artery revascularisation.

   c. Peripheral arterial disease (PAD):

   1. History of prior percutaneous or surgical revascularisation of an iliac, femoral, or popliteal artery or aortic aneurysm in electronic patient history
   2. Prior surgical amputation of a lower extremity due to peripheral artery disease.

   OR ASCVD risk equivalents as per assessed by the online tool (>10% probability of CVD event within the next 5 years www.cvdcheck.org.au/calculator) or at clinically determined high risk.

4. Serum LDL-C above target ≥1.8 mmol/L (≥70 mg/dL) for ASCVD patients or ≥2.0 mmol/L for ASCVD risk equivalent patients
5. Not at Guideline directed cholesterol goals
6. On a stable dose of lipid-lowering therapy (such as a statin and/or ezetimibe) for ≥30 days before screening with no planned medication or dose change. Statin intolerant patients are eligible if intolerance is documented.

Exclusion Criteria:

1. Any medical or surgical history and or condition that might limit the individual's ability to take part in the study and/or put the participant at significant risk (according to physician's judgment).
2. Any underlying known disease, or surgical, physical, or medical condition that, in the opinion of the physician might interfere with the interpretation of the study results, including pregnancy.
3. Previous, current, or planned treatment with a monoclonal antibody targeting PCSK9.
4. Participants unable to access or unwilling to use mobile phone to receive text messages and/or questionnaires as proposed in the new model of care.
5. Participants who plan to move away from the geographical area where the study is being conducted during the study period.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Usual Care Model; Usual care arm : The GPs will be educated on the ESC guidelines and Guideline Directed Management therapy (GDMT) Inclisiran is available for this arm	Drug: Inclisiran Prefilled Syringe; Inclisiran, 284 mg, 1.5 ml Liquid in a single-use prefilled syringe (PFS) for s.c. administration and any standard medications to be used within registered indication and at the treating physician's discretion.; Other Names: LEQVIO
Other: New Model of Care; Model of care arm The GPs will be educated on the ESC guidelines and Guideline Directed Management therapy (GDMT) The Participants enrolled via these sites arm will be getting receive monthly SMS messages with regards to regarding cardiovascular health and appointment reminders (low touch engagement nudges) In addition, Participants will receive telephone-based support calls from a study nurse trained in motivational interviewing. These telephone calls will cover diet, exercise, medication, and where necessary smoking cessation. A summary of any recommendations will then be sent to the primary care physician via email or letter. Inclisiran is available for this arm.	Drug: Inclisiran Prefilled Syringe; Inclisiran, 284 mg, 1.5 ml Liquid in a single-use prefilled syringe (PFS) for s.c. administration and any standard medications to be used within registered indication and at the treating physician's discretion.; Other Names: LEQVIO; Other: SMS messages; Participants will receive monthly SMS messages regarding cardiovascular health (low touch engagement nudges); Other Names: Monthly Text Messages; Other: Telephone-based support calls; Participants will receive telephone-based support calls from a study nurse trained in motivational interviewing. These telephone calls will cover diet, exercise, medication, and where necessary smoking cessation. A summary of any recommendations will then be sent to the primary care physician via email or letter.; Other Names: Nurse Support Calls

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effect on LDL-C Concentration	LDL-C concentration at baseline and at day 180	Baseline and 180 Days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effect on LDL-C Concentration	LDL-C concentration at baseline and at day 365	365 Days

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Medication adherence	Proportion of patients reporting high levels of adherence to lipid lowering therapy between both arms.	365 Days
Lowering absolute cardiovascular (CV) risk	Absolute risk at day 180 as assessed by the CVD Check Calculator: www.cvdcheck.org.au/calculator).	180 Days
Health care resourcing consumption	The health care resourcing consumption of each of the models of care as assessed by Medicare item number utilisation if feasible.	180 and 365 Days
Lp(a) levels	Lp(a) levels at baseline and day 180	180 Days
Changes in Lp(a) levels	The percentage change in Lp(a) from baseline to Day 180	180 Days
Patient satisfaction- Client Satisfaction Questionnaire	CSQ-8 (Client Satisfaction Questionnaire) score at baseline, and days 180 and 365-Total scores range from. 8 to 32 with the higher number indicating greater satisfaction	Baseline,180 and 365 Days
Patient Activation Measure	Patient activation measure (PAM) questionnaire score at baseline, and days 180 and 365 (Raw scores are transformed to a scaled of 0-100 ith higher PAM scores indicating higher patient activation)	Baseline,180 and 365 Days
LDL-C Concentration control	Concentration of serum LDL-C to target (Primary prevention <2.0 mmol/L, Secondary prevention <1.8mmol/L, and secondary prevention for patients at very high risk <1.4mmol/L)	90 and 270 Days
Blood Pressure Measure- Control over Risk factors	Blood pressure value <130mmHg	90 and 270 Days
HbA1c Value - Control over Risk factors	HbA1c Value <7%	90 and 270 Days
BMI Value - Control over Risk factors	BMI <25kg/m2 (BMI is calculated by dividing the weight in Kilograms by the height in meters)	90 and 270 Days
Identify potential opportunities and challenges that can have an effect on scalability of the model of care for a broader population-1	Characterise study sites and their relationship to Intensification of LDL-C lowering therapy as per GDMT.	180 and 365 Days
Identify potential opportunities and challenges that can have an effect on scalability of the model of care for a broader population-2	Characterise patients' demographics and their relationship to Intensification of LDL-C lowering therapy as per GDMT.	180 and 365 Days
Identify potential opportunities and challenges that can have an effect on scalability of the model of care for a broader population-3	Characterise study sites and their relationship to effectiveness of CV risk factor lowering.	180 and 365 Days
Identify potential opportunities and challenges that can have an effect on scalability of the model of care for a broader population-4	Characterise patients' demographics and their relationship to effectiveness of CV risk factor lowering.	180 and 365 Days

Collaborators and Investigators

• Sponsor: Monash University
• Collaborators: Novartis Pharmaceuticals
• Investigators: Principal Investigator: Stephen Nicholls, Monash Heart

Study record dates

Study Major Dates

• Study Start (Actual): November 17, 2023
• Primary Completion (Estimated): June 1, 2024
• Study Completion (Estimated): June 1, 2025

Study Registration Dates

• First Submitted: February 20, 2023
• First Submitted That Met QC Criteria: April 17, 2023
• First Posted (Actual): April 28, 2023

Study Record Updates

• Last Update Posted (Actual): January 11, 2024
• Last Update Submitted That Met QC Criteria: January 9, 2024
• Last Verified: January 1, 2024

More Information

Terms related to this study

• Keywords: Secondary Cardiovascular Prevention; Atherosclerotic Cardiovascular Disease (ASCVD); Lipid lowering therapies; Hypercholesterolaemia; Hyperlipidaemia; New Model of Care; Nurse-Led Support Calls; Guideline Directed Management therapy (GDMT); The European Society of Cardiology (ESC) Guidelines
• Additional Relevant MeSH Terms: Vascular Diseases; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Arteriosclerosis; Arterial Occlusive Diseases; Heart Diseases; Coronary Artery Disease; Myocardial Ischemia; Coronary Disease; Cardiovascular Diseases; Peripheral Arterial Disease; Peripheral Vascular Diseases; Atherosclerosis; Cerebrovascular Disorders
• Other Study ID Numbers: CKJX839A1AU03R

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No