Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07447362

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

Led by Universidad Católica San Antonio de Murcia · Updated on 2026-03-03

220

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating cardiovascular risk factors and clinical outcomes in adults attending an outpatient cardiology clinic. The study aims to identify predictors of adverse cardiovascular events, improve risk assessment, and enhance preventive care during routine clinical practice. Data collection will occur without changing participants' current treatments, focusing on a better understanding of cardiovascular risk profiles to support improved patient management. Participants will receive structured clinical and pharmacological management based on established guidelines. This includes regular assessments and adjustments of treatments for blood pressure, cholesterol, blood sugar, and lifestyle factors over a 120-day follow-up period. The intervention involves protocol-based management of antihypertensive, lipid-lowering, antidiabetic medications, and lifestyle recommendations. During the study, participants will undergo periodic evaluations of various health measures such as blood pressure, cholesterol levels, blood sugar, body weight, kidney function, and urine markers. These outcomes will be monitored from baseline to 90 days to assess changes. The study involves scheduled follow-up visits to track cardiovascular risk changes and ensure appropriate management, with a total participation duration extending over approximately four months.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 63 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
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 120 days

Participants receive structured clinical follow-up with periodic assessment of cardiovascular risk factors and adjustment of pharmacological and lifestyle management according to current clinical guidelines.

Periodic visits over 120 days

Trial Site Locations

Total: 1 location

1

CDIEM Medical Center - Outpatient Cardiology Clinic

Santiago, Santiago Metropolitan, Chile

Actively Recruiting

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Research Team

J

Julio César Núñez Farías, MD, MSc (Cardiology)

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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