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RecruitingNCT07294937Updated Dec 19, 2025

Study Protocol: 10-Year Follow-Up of Patients Screened for Cardiovascular Risk by the "All With Heart" Association - Development of a Morocco-Specific Risk Score

An observational study in Cardiovascular Diseases (CVD), sponsored by Moroccan Society of Cardiology. Recruiting at 2 sites in Morocco. Open to participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2025-12-19.

Sponsored by Moroccan Society of Cardiology · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Oct 2025; still recruiting 1 year 1 month later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
10,000
Ages
40 Years and older
Sex
All
01

Study summary

Cardiovascular diseases (CVDs) are the leading cause of death worldwide, and their prevalence is steadily increasing in Morocco. Between 2010 and 2012, the "All with heart" Association conducted a large-scale cardiovascular screening campaign in the Greater Casablanca region, involving more than 10,000 adults aged over 40 years. This 10-year follow-up study aims to evaluate long-term cardiovascular outcomes and to develop a Morocco-specific cardiovascular risk score. Follow-up data will be collected through phone calls, WhatsApp, or SMS with participants or their families to document cardiovascular deaths, myocardial infarctions, and strokes. Statistical analyses, including survival analysis and multivariate logistic regression, will be used to identify significant risk factors and to construct a predictive risk model tailored to the Moroccan population. The study received a favorable opinion from the Rabat Ethics Committee. Written informed consent will be obtained from all participants or their families prior to data collection. The findings are expected to enhance understanding of cardiovascular risk evolution in Morocco and to provide a validated, population-specific risk score to support prevention and patient management strategies.

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Conditions studied

  • Cardiovascular Diseases (CVD)
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In context

Cardiovascular Diseases

5,368 studies on the registry are indexed under Cardiovascular Diseases; 939 are open to participants now.

This study's planned enrollment of 10,000 is above the median of 506 across 1,572 observational studies indexed under Cardiovascular Diseases.

Browse Cardiovascular Diseases studies →

Lead sponsor

Moroccan Society of Cardiology is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population includes adults aged 40 years and older who were screened for cardiovascular risk between 2010 and 2012 by the "All with heart" Association in the Greater Casablanca region, Morocco. Approximately 10,000 individuals participated in the original screening campaign, which collected data on anthropometric, biological, and lifestyle risk factors.

For the 10-year follow-up, all eligible Moroccan participants from the initial screening will be contacted by phone, WhatsApp, or SMS to collect updated information on cardiovascular events, hospitalizations, and mortality. This population represents a community-based cohort reflecting the general adult population at risk of cardiovascular disease in Morocco.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 for participation in the 10-year follow-up study.

Exclusion criteria

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.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
10,000 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • Participants screened for cardiovascular risk (TAC cohort)

    Participants aged 40 years and older who were screened for cardiovascular risk between 2010 and 2012 by the "All with heart" Association in the Greater Casablanca region. This cohort is being followed 10 years after the initial screening to assess cardiovascular outcomes (death, myocardial infarction, stroke) and to develop a Morocco-specific cardiovascular risk score. No intervention is applied; the study is purely observational.

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What researchers measure

Primary outcomes

  1. Incidence of Major Cardiovascular Events (MACE)

    Occurrence of major cardiovascular events (myocardial infarction, stroke, or cardiovascular death) among participants screened for cardiovascular risk between 2010 and 2012 by the "All with heart" Association. Events will be identified during the 10-year follow-up period through participant or family contact (phone, WhatsApp, or SMS) and verified through available medical records when possible.

    Time frame: 10 years after initial screening (2010-2012)

  2. Development and Validation of a Morocco-Specific Cardiovascular Risk Score

    Development and internal validation of the Morocco-Specific Cardiovascular Risk Score, a composite risk prediction score estimating the 10-year probability of major cardiovascular events including myocardial infarction, stroke, or cardiovascular death. The score will be derived from baseline cardiovascular risk factors collected during the initial screening and weighted using multivariable regression models based on outcomes observed during the 10-year follow-up. The score will be expressed on a scale ranging from 0 to 100, where higher scores indicate a higher cardiovascular risk and therefore a worse outcome. Model performance will be assessed using discrimination and calibration measures, including the area under the receiver operating characteristic curve and calibration analyses.

    Time frame: Baseline (2010-2012) and 10-year follow-up (2022)

Secondary outcomes

  1. Incidence of Minor Cardiovascular Events

    Occurrence of minor cardiovascular events, including stable or unstable angina, among participants screened between 2010 and 2012. Events will be collected through participant or family interviews and verified with medical records when available.

    Time frame: 10 years after initial screening (2010-2012)

Other outcomes

  1. Number of Hospitalizations Related to Cardiovascular Diseases

    Total number of hospitalizations due to cardiovascular causes (acute coronary syndrome, heart failure, arrhythmia, or cardiac surgery) during the 10-year follow-up period.

    Time frame: 10 years after initial screening (2010-2012)

  2. Change in Cardiovascular Risk Factors Over Time

    Change in major cardiovascular risk factors (body mass index, blood pressure, total cholesterol, triglycerides, HDL, blood glucose, smoking status, and physical activity) between the initial screening and the 10-year follow-up.

    Time frame: 10 years after initial screening (2010-2012)

  3. Quality of Life Assessment

    Evaluation of participants' quality of life using a standardized questionnaire (EQ-5D). The assessment will explore mobility, self-care, usual activities, pain/discomfort, and anxiety/depression dimensions.

    Time frame: 10 years after initial screening (2010-2012)

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Study locations

2 of 2 sites recruiting
  • Moroccan Society of Cardiology
    Casablanca, 20200, Morocco
    Recruiting
  • Cardiology Centre, Mohammed V Military Hospital, Rabat, Morocco
    Rabat, Morocco
    Recruiting
    • Najat MOUINE, Professor of Cardiology · Contactmouine2@yahoo.fr · +212661202733
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References and documents

Individual participant data

Plan to share: No — The sharing of individual participant data (IPD) is not authorized by the Ethics Committee of Rabat. According to the committee's decision, data collected in this study are strictly confidential and may only be used by the research team for the purposes defined in the approved protocol. All collected data will remain stored securely and will not be shared with other researchers or institutions to ensure compliance with national data protection regulations and the ethical approval obtained for this study.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07294937
Lead sponsor
Moroccan Society of Cardiology
Collaborators
F&C Clinical Trials
Responsible party
Sponsor
First posted
Dec 19, 2025
Start date
Oct 1, 2025
Primary completion
Mar 2026 (estimated)
Completion
Oct 2026 (estimated)
Last update
Dec 19, 2025

Study contacts

Najat MOUINE, Professor of Cardiology
Contact
mouine2@yahoo.fr
+212661202733
Mohamed ALAMI
Contact

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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