10-year follow-up of adults screened for heart risk to create a Morocco-specific heart risk score

Is this trial a fit for you?

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

What this trial studies

Researchers will re-contact more than 10,000 adults who participated in a 2010–2012 cardiovascular screening in Greater Casablanca to document cardiovascular deaths, heart attacks, and strokes using phone calls, WhatsApp, or SMS. Follow-up outcomes will be combined with baseline screening data to perform survival analysis and multivariable logistic regression. The team will use those results to develop and internally validate a predictive risk model specific to the Moroccan population. The project is coordinated by the Moroccan Society of Cardiology with clinical sites in Casablanca and Rabat and requires written informed consent for participation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults aged 40 years or older at the time of the initial screening (2010-2012).
* Individuals who participated in the cardiovascular risk screening campaign conducted by the "All with heart" Association between 2010 and 2012 in the Greater Casablanca region.
* Moroccan nationality.
* Participants or family members who provide written informed consent for participation in the 10-year follow-up study.

Exclusion Criteria:

* Individuals who refuse to participate in the follow-up study.
* Participants who have moved and cannot be reached by phone, WhatsApp, or SMS.
* Participants who died from non-cardiovascular causes.
* Non-Moroccan participants.

Where it's running

• Moroccan Society of Cardiology
  Casablanca, Morocco Recruiting
• Cardiology Centre, Mohammed V Military Hospital, Rabat, Morocco
  Rabat, Morocco Recruiting

Study contacts

• Study coordinator: Najat MOUINE, Professor of Cardiology
• Email: mouine2@yahoo.fr
• Phone: +212661202733

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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.