Clinical Management of Cardiovascular Risk Factors in Adult Patients: A Before-and-After Interventional Study
CV-RISK
Effect of a Structured Clinical and Pharmacological Management Strategy on Cardiovascular Risk Factors in Adult Patients in Routine Clinical Practice: A Pseudo-Experimental Before-and-After Study
1 other identifier
interventional
220
1 country
1
Brief Summary
This study aims to evaluate cardiovascular risk factors, clinical characteristics, and outcomes in adult patients attending an outpatient cardiology clinic. The research focuses on identifying predictors of adverse cardiovascular events, optimizing risk stratification, and improving preventive strategies in routine clinical practice. Data will be collected from patients receiving standard cardiology care without altering their treatment. The results are expected to contribute to better understanding of cardiovascular risk profiles and to support improvements in clinical decision-making and patient management.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 24, 2024
CompletedFirst Submitted
Initial submission to the registry
February 24, 2026
CompletedFirst Posted
Study publicly available on registry
March 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 24, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 24, 2026
ExpectedMarch 3, 2026
February 1, 2026
2 years
February 24, 2026
February 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in systolic blood pressure
Change in systolic blood pressure (mmHg) measured under standardized conditions to evaluate the effect of structured clinical and pharmacological cardiovascular risk management.
Baseline to 90 days
Secondary Outcomes (11)
Change in diastolic blood pressure
Baseline to 90 days
Change in LDL cholesterol
Baseline to 90 days
Change in HbA1c
Baseline to 90 days
Change in body weight
Baseline to 90 days
Change in renal function (eGFR)
Baseline to 90 days
- +6 more secondary outcomes
Study Arms (1)
Structured Clinical Management
EXPERIMENTALParticipants receive structured clinical follow-up with periodic assessment of cardiovascular risk factors and adjustment of pharmacological and lifestyle management according to current clinical guidelines over a 120-day follow-up period.
Interventions
Protocol-based clinical management including periodic evaluation and adjustment of antihypertensive, lipid-lowering, antidiabetic, and lifestyle interventions according to routine clinical practice guidelines.
Eligibility Criteria
You may qualify if:
- Age ≥18 years
- Presence of at least one cardiovascular risk factor (hypertension, diabetes, dyslipidemia, obesity, or smoking)
- Receiving outpatient clinical follow-up
- Ability to provide informed consent
You may not qualify if:
- Severe clinical instability requiring hospitalization
- Pregnancy
- End-stage renal disease or dialysis
- Inability to complete follow-up visits
- Refusal to participate
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CDIEM Medical Center - Outpatient Cardiology Clinic
Santiago, Santiago Metropolitan, Chile
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
José Abellán Alemán, MD, PhD
Universidad Católica San Antonio de Murcia
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Cardiologist and Principal Investigator
Study Record Dates
First Submitted
February 24, 2026
First Posted
March 3, 2026
Study Start
July 24, 2024
Primary Completion
July 24, 2026
Study Completion (Estimated)
October 24, 2026
Last Updated
March 3, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy regulations and institutional data protection policies. De-identified aggregated results will be available through scientific publication.