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Clinical Management of Cardiovascular Risk Factors in Adult Patients: A Before-and-After Interventional Study

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07447362
Acronym
CV-RISK
Enrollment
220
Registered
2026-03-03
Start date
2024-07-24
Completion date
2026-10-24
Last updated
2026-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factors, Dyslipidemia, Hypertension, Obesity, Overweight, Tobacco Use, Type 2 Diabetes Mellitus

Keywords

Cardiovascular prevention, Risk factor control, Medication adherence, Clinical follow-up

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.

Interventions

OTHERStructured Cardiovascular Risk Management

Protocol-based clinical management including periodic evaluation and adjustment of antihypertensive, lipid-lowering, antidiabetic, and lifestyle interventions according to routine clinical practice guidelines.

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants receive structured clinical follow-up with periodic evaluation and adjustment of standard pharmacological therapy under routine clinical practice using a before-and-after design.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* Severe clinical instability requiring hospitalization * Pregnancy * End-stage renal disease or dialysis * Inability to complete follow-up visits * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Change in systolic blood pressureBaseline to 90 daysChange in systolic blood pressure (mmHg) measured under standardized conditions to evaluate the effect of structured clinical and pharmacological cardiovascular risk management.

Secondary

MeasureTime frameDescription
Change in diastolic blood pressureBaseline to 90 daysEvaluation of changes in diastolic blood pressure following structured clinical and pharmacological management.
Change in LDL cholesterolBaseline to 90 daysEvaluation of changes in LDL cholesterol measured during routine laboratory assessment after structured cardiovascular risk management.
Change in HbA1cBaseline to 90 daysEvaluation of changes in glycated hemoglobin (HbA1c) following structured cardiovascular risk management.
Change in body weightBaseline to 90 daysEvaluation of changes in body weight following lifestyle counseling and structured cardiovascular risk management.
Change in renal function (eGFR)Baseline to 90 daysEvaluation of changes in renal function assessed by estimated glomerular filtration rate following structured cardiovascular risk management.
Change in HDL cholesterolBaseline to 90 daysEvaluation of changes in HDL cholesterol measured during routine laboratory assessment after structured cardiovascular risk management.
Change in triglyceridesBaseline to 90 daysEvaluation of changes in triglyceride levels measured during routine laboratory assessment after structured cardiovascular risk management.
Change in total cholesterolBaseline to 90 daysEvaluation of changes in total cholesterol measured during routine laboratory assessment after structured cardiovascular risk management.
Change in fasting plasma glucoseBaseline to 90 daysEvaluation of changes in fasting plasma glucose following structured cardiovascular risk management.
Change in body mass indexBaseline to 90 daysEvaluation of changes in body mass index following lifestyle counseling and structured cardiovascular risk management.
Change in microalbuminuriaBaseline to 90 daysEvaluation of changes in urinary albumin excretion to assess microalbuminuria during follow-up after structured cardiovascular risk management.

Countries

Chile

Contacts

CONTACTJulio César Núñez Farías, MD, MSc (Cardiology)
llaillai@yahoo.es+56965860130
STUDY_CHAIRJosé Abellán Alemán, MD, PhD

Universidad Católica San Antonio de Murcia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026