iHeart DepCare for Depression in Heart Disease Patients
This study is testing a tool called iHeart DepCare to help people with heart disease who also have depression. The iHeart DepCare tool is an electronic program that helps bridge depression screening with treatment. It includes information about depression symptoms and behavioral risk factors. Researchers want to see if using this tool helps more people start or continue treatment for their depression. You may be able to join if you are over 18, have heart disease, and have certain scores on a depression screening. The study aims to enroll 200 participants. The current status of the study is unclear.
- Study design
- This is an interventional study that plans to enroll 200 participants. Participants will be randomly assigned to either receive usual care or the iHeart DepCare tool with support.
- What's involved
- Participants will receive the iHeart DepCare tool along with brief motivational, technical, and navigation support based on their preference. Depression treatment initiation or intensification will be measured for up to 6 months.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for up to 6 months to measure whether they start or intensify depression treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Patient Activation Approach to Implementing Depression Treatment in Cardiac Patients
At a glance
Conditions
NCT07390331
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Columbia University Irving Medical Center
New York, New Yorkstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Nathalie Moise, MD, MS, FAHA · PRINCIPAL_INVESTIGATOR · Columbia University
Who to contact
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Inclusion
Exclusion
What this trial measures
- Percentage of eligible patients who initiate or intensify depression treatmentUp to 6 months
This is designed to measure depression treatment reach, which is defined as the percentage of eligible patients who initiate or intensify depression treatment within 6 months of the index visit, as indicated by ≥1 pharmacy fill data of a new or changed antidepressant and/or a new visit with a mental health provider (e.g., psychologist, psychiatrist, behavioral health provider like social workers) and/or primary care provider with a visit diagnosis of depression and/or an exercise program (e.g., cardiac rehabilitation), which will be assessed through chart extraction and tallied.