Clinical trial Recruiting at 1 site Interventional Ages 40 and up

Group visits to help manage high cholesterol

Official title: Improving Care Through Group Medical Visits for Patients With Dyslipidemia

Run by Université de Sherbrooke · NCT07543718 · Data updated 2026-11-12

This project will try group medical visits for adults with dyslipidemia to see if they improve care, lifestyle habits, and access to primary care.

Quick facts

Study typeInterventional
Ages40 Years and up
SexAll
Enrollment288 (estimated)
SponsorUniversité de Sherbrooke
Academic / other
Locations1 site (Dieppe, New Brunswick)
StatusRecruiting
StartedApril 2026
Main results expectedJanuary 2030
Study endsDecember 2030
Registry record updatedApril 22, 2026
Trial IDNCT07543718 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with dyslipidemia meeting Canadian Cardiovascular Society criteria — at minimum an intermediate Framingham cardiovascular risk (10–19.9%) with LDL‑C ≥ 3.5 mmol/L or non‑HDL‑C ≥ 4.2 mmol/L or ApoB ≥ 1.05 g/L — who can attend in-person group sessions and provide informed consent.

Probably not a fit

Patients unable to participate in group sessions, those with severe cognitive impairment or recent acute psychiatric decompensation, or those with a terminal illness and life expectancy under 12 months are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Group medical visits (GMVs) replace one-on-one primary care appointments with scheduled sessions for patients who share a condition, combining medical assessment, education, prescriptions, and peer discussion. This project will implement GMVs for 144 patients with dyslipidemia at a primary care unit in Dieppe, New Brunswick, and collect data on how the approach is delivered and received. Clinical indicators (including lipid levels), patient-reported outcomes, and health service use will be tracked alongside measures of feasibility and acceptability. The goal is to document whether GMVs can be integrated into routine primary care and whether they affect health behaviors, access, and clinical outcomes.

Why it matters

Potential benefit: If successful, GMVs could improve cholesterol control and lifestyle habits, increase access to primary care, and reduce pressure on healthcare services.

How similar studies have gone: GMVs have shown benefits for diabetes and other chronic conditions in prior studies, but they have not been specifically tested for dyslipidemia.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosis of dyslipidemia according to the guidelines of the Canadian Cardiovascular Society, i.e., at a minimum: an intermediate cardiovascular risk according to the Framingham Risk Score (10-19.9%) WITH LDL-C ≥ 3.5 mmol/L or non-HDL-C ≥ 4.2 mmol/L or ApoB ≥ 1.05 g/L

Exclusion Criteria:

* Patients unable to participate in GMV sessions or to provide informed consent

  * Patients with a mental health condition likely to limit their ability to benefit from GMV sessions and discussions (Examples: severe dementia or an acute psychiatric decompensation occurring within the past six months)
  * A diagnosis of terminal illness or a life expectancy of less than 12 months

Where it's running

  • Unité de médecine familiale du Grand-Moncton
    Dieppe, New Brunswick, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.