Phone-Based cholesterol coaching after heart attack shows promise
NCT ID NCT07685639
First seen Jul 06, 2026 · Last updated Sep 10, 2026 · Updated 3 times
Summary
This study tests whether a proactive, pharmacist-led telephone program can help people who have had a heart attack reach safer cholesterol levels. Participants receive pharmacist calls, repeat blood tests, and medication adjustments based on national guidelines. The goal is to see if this approach increases the number of patients who achieve an LDL cholesterol target below 1.8 mmol/L at six months, compared to usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pharmacist-led lipid optimization pathway (telephone clinic)
- What this could lead to
- If successful, this approach could become a standard way to help heart attack survivors achieve healthier cholesterol levels and lower their risk of future heart attacks or strokes.
- What could go wrong
- This is a quality improvement study, not a test of a new drug. The results may not apply outside Alberta, and the program may not work as well in other healthcare settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adults over the age of 18 2. Resident of Alberta 3. Individuals hospitalized with an acute coronary syndrome and have undergone coronary angiography. 4. Able to participate in follow-up contact if randomized to the intervention arm Exclusion Criteria: 1\. In-hospital mortality
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Alberta Hospital / Mazankowski Alberta Heart Institute
RECRUITINGEdmonton, Alberta, T6G2B7, Canada
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University of Alberta Hospital / Mazankowski Alberta Heart Institute
RECRUITINGEdmonton, Alberta, T6G3B7, Canada
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