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Clinical Trials in Canada / NCT07313657
Recruiting Not applicable

Improving Care and Mental Well-Being for Adults With Heart Failure

NCT07313657 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-09-26
Last updated
2026-02-17

Condition(s) studied

Heart FailureMental HealthStressAnxietyDepression

Investigational drug(s) / intervention(s)

Heart Failure and Mental Health Intervention (FRAME)

Heart Failure and Mental Health Intervention (FRAME): Foundation, Recognition, Awareness, Management and Engagement (FRAME) is a multi-component, co-designed web tool created in collaboration with patient partners, caregivers, healthcare providers, and Archipel and Great River Ontario Health Teams. It is designed to improve recognition, awareness, management and support for mental health in patients with heart failure. There are three different versions: one for healthcare providers, one for caregivers and one for patients. The intervention includes educational material about heart failure and mental health, conversational support to help facilitate discussions about mental health, self-management activity maps (e.g., tips about nutrition and exercise), asset maps (i.e., displaying available resources), and the provider-facing discussion tool to help initiate conversations about mental health and guide referrals or supports. FRAME was developed through a co-design process informed by the lived experiences of community partners.

Study summary

Heart failure is a high-risk, chronic condition that impacts patients' mental health. Approximately 50% of heart failure patients experience comorbid mental health conditions, such as stress, depression and anxiety, which affect their day-to-day lives. Despite this interconnection, the integration of mental health awareness and support into cardiac care remains limited. To address this gap, the FRAME (Foundation, Recognition, Awareness, Management, Engagement) intervention was co-designed by researchers, healthcare providers, health system decisionmakers, and patient partners. This pilot study evaluates the feasibility of implementing the FRAME intervention in pilot clinical sites within two health regions in Ontario, Canada, including team-based family medicine clinics, cardiac rehabilitation/specialist clinics, and emergency departments. Utilizing a pretest-posttest hybrid 1 model intervention design, this study evaluates process indicators and patient-focused outcomes through surveys and semi-structured qualitative interviews. Findings from this study will inform a future large scale cohort study and scalable integration of the FRAME tool into existing cardiac care pathways to enhance mental health awareness and support among heart failure patients.

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: For Patients (Surveys and Optional Interviews): * Patients at risk of heart failure (e.g., irregular heartbeat, coronary artery disease, a past heart attack, high blood pressure that is being treated, cardiomyopathy), or with a self-reported/documented diagnosis of heart failure OR on the following list of medications : * Angiotensin receptor-neprilysin inhibitors (ARNI), called sacubitril-valsartan * Angiotensin converting enzyme inhibitors (ACEi), called "prils" * Angiotensin-receptor blockers (ARBs), called "sartans" * Beta-blockers, called "lols" * Mineralocorticoid receptor antagonists (MRAs) * Sodium-glucose co-transporter-2 (SGLT2) inhibitors, called "flozins" * Receiving care at one of the participating pilot test sites or if they found their way to the tool website * Willing and able to provide informed consent and name, email address and phone number for follow-up contact (for survey and interview) Caregivers (Optional interviews): * Caregivers who support adult(s) with heart failure. Exclusion Criteria: * Inability to provide informed consent (e.g., due to cognitive impairment or language barriers without translated support) * Participants who do not have access to the internet will not be able to use the web-tool. For Healthcare Providers * Providers that are not involved in the care of heart failure patients

Primary outcome measure(s)

Trial sites (9)

FacilityCityRegionStatus
Seaway Valley Community Health Centre (Cardiac Rehab Program) Cornwall Ontario Recruiting
Centre de Santé Communautaire de l'Estrie Limoges Ontario Active Not Recruiting
Orleans Cardiopulmonary Clinic Orléans Ontario Recruiting
Bruyère Health Research Institute Ottawa Ontario Not Yet Recruiting
Byward Family Health Team Ottawa Ontario Not Yet Recruiting
Montfort Hospital, and associated Aline-Chrétien Rehabilitation Clinic Ottawa Ontario Active Not Recruiting
Ste-Anne Medical Clinic Ottawa Ontario Active Not Recruiting
University of Ottawa Heart Institute Ottawa Ontario Active Not Recruiting
Winchester Memorial Hospital Winchester Ontario Recruiting

More Bruyère Health Research Institute. trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07313657 on ClinicalTrials.gov ↗ ← All trials in Canada