A Hospital-Based Registry of Preventive Cardiology Clinics (PREVENT-CARD)

National Institute of Cardiovascular Diseases, Pakistan

Status: Enrolling

Conditions: Cardiovascular Morbidity; Primary Prevention CVD; Cardiovascular Risk Assesment

Treatments: Other: Cardiovascular risk assesment

Study type: Observational

Funder types: Other

Identifiers

NCT06503341

IRB-20/2023

Details and patient eligibility

About

More research is needed to articulate the most effective ways to use these tools as screening tests in cardiovascular risk assessments and how they ultimately affect CVD mortality and morbidity outcomes. Clinicians are encouraged to continue sharing decision-making with patients to combine their unique cardiovascular risk factors and develop a comprehensive, effective treatment plan.

Full description

Study Design: observational study Duration of Study: ongoing. Sample Size: All patients presenting to preventive cardiology clinics at the National Institute of Cardiovascular Diseases (NICVD), Karachi, Pakistan..

Sampling Technique: Non-probability consecutive sampling Data Collection Procedure: Verbal informed consent will be obtained from all the patients regarding their participation in the study and publication of study findings while maintaining confidentiality. Consecutive patients presenting preventive cardiology clinics at the National Institute of Cardiovascular Diseases (NICVD), Karachi, Pakistan, will be included in this registry. Demographic characteristics, physical examination, clinical history, risk modification, lab assessment, and ASCVD risk score at presentation and at every follow-up will be recorded using a structural questionnaire.

Data Analysis Procedure: The Tentative analysis plan uses collected data for research publications. The statistical package for social sciences (SPSS 21) will be used to analyze baseline characteristics. The Shapiro-Wilk test will be applied to check the hypothesis of normality for quantitative (continuous) variables. Descriptive statistics such as mean ± SD, median (IQR), skewness, maximum, and minimum will be calculated for quantitative (continuous) variables. Frequency and percentages will be calculated for categorical variables.

Enrollment: 10,000 estimated patients

Sex: All

Ages: 18 to 90 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• All individuals attending the preventive cardiology clinics.

Exclusion criteria

• • Individuals who refused to give consent.

Trial design

10,000 participants in 1 patient group

Adult patients

Description:

Adult patients with or without cardiovascular diseases.

Treatment:

Other: Cardiovascular risk assesment