Ireland
--:--IST
Recruiting Not applicable

Effect of Early Educational Intervention on Cardiovascular Risk Factors After Acute Coronary Syndrome

NCT07402642 · tracked via the Priya Life Science Spain tracker
Sponsor
Sergio Mies Padilla
Phase
Not applicable
Started
2026-01-12
Last updated
2026-02-11

Condition(s) studied

Myocardial Infarction

Investigational drug(s) / intervention(s)

Motivational and Individualized InterviewingHeart-Healthy Dietary EducationTobacco Cessation ApproachPhysical Activity PromotionEmotional Health ManagementTherapeutic Adherence ReinforcementSelf-Control TrainingUse of Educational ResourcesCardiac Rehabilitation Program

Motivational and Individualized Interviewing: Used to verify the patient's understanding of their condition and to motivate behavioral changes.

Heart-Healthy Dietary Education: Specific counseling to improve adherence to the Mediterranean diet and address overweight or obesity

Tobacco Cessation Approach: Interventions aimed at increasing motivation to quit smoking and reducing nicotine dependence

Physical Activity Promotion: Personalized exercise recommendations tailored to the patient's clinical status

Emotional Health Management: Professional support to address emotional well-being, detecting potential states of anxiety or depression following the acute event.

Therapeutic Adherence Reinforcement: Continuous education and monitoring to ensure compliance with the prescribed pharmacological plan

Self-Control Training: Training the patient for autonomous monitoring of risk factors, such as blood pressure

Use of Educational Resources: Provision of adapted materials (infographics and written documents) to permanently reinforce healthy knowledge and behaviors

Cardiac Rehabilitation Program: Upon hospital discharge, all patients are referred to a cardiac rehabilitation unit. The program consists of an average of 17 sessions focused primarily on the physical rehabilitation of the patient. Patients receive group-based health education provided by nursing professionals during these sessions.These rehabilitation sessions are typically completed within three months following the coronary event. Patients continue to receive medical and nursing attention through specialized care centers or primary care. Both groups receive optimal pharmacological treatment and general advice on cardiovascular health, including physical activity and diet.

Study summary

Early Education After a Heart Attack What is the purpose of this study? The main goal is to evaluate if a special nursing education and support program helps patients who have suffered a heart attack feel more confident in managing their own health. Researchers want to see if this extra support improves how patients care for their hearts through diet, physical activity, and quitting smoking. The study compares this new nursing strategy against the standard care patients usually receive.

Who can participate? Participants must be 18 years of age or older. People who have recently had a heart attack requiring an urgent heart catheterization at the Complejo Hospitalario Universitario Insular Materno Infantil.

Exclusions: People with significant language barriers (Spanish), mental incapacity to follow recommendations, or those unable to attend in-person consultations cannot participate.

What will happen during the study? Participants will be divided into two groups: Standard Care Group (Control): These participants will receive the usual medical follow-up and standard cardiac rehabilitation sessions (an average of 17 sessions focused on exercise and group education). Special Support Group (Experimental): In addition to standard care, these participants will have a specific nursing consultation consisting of 4 scheduled visits.

These visits are a mix of in-person and telephone appointments.Nurses will provide personalized educational materials, such as infographics, and teach techniques to control blood pressure, improve diet, exercise safely, and manage emotions after a heart attack.

Duration and Follow-up Each participant will be followed for approximately 8 months. During this time, they will be asked to complete several surveys about their lifestyle.

Researchers will also review blood test results (cholesterol levels) from their medical records to track progress.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients must have suffered an Acute Myocardial Infarction. * Participants must have undergone an urgent cardiac catheterization. * Specifically, this includes patients who received coronary reperfusion strategies following the activation of the CODICAN protocol (assistance for ST-segment elevation myocardial infarction) within the study environment. Exclusion Criteria: * Patients with little or no knowledge of the Spanish language that prevents effective communication or reading of educational resources. * Patients unable to understand their participation or follow health recommendations independently. * Patients with an unfavorable clinical prognosis or those requiring hospitalization for a period exceeding established limits. * Patients unable to attend in-person nursing consultations due to personal reasons or place of residence

Primary outcome measure(s)

  • Cardiac Self-Efficacy — Experimental Group: measured at two time points: baseline (during hospitalization) and 8 months (post-coronary event). Control Group: measured only at the 8-month mark post-coronary event to evaluate the level of self-efficacy after receiving standard
    His measure evaluates specific behaviors related to cardiovascular health using the Spanish-validated version of the Cardiac Self-Efficacy Scale (S-CSE). This tool consists of 12 items across three dimensions: symptom control, disease control, and activity maintenance. Each item is rated on a 7-point Likert scale (1 = not at all confident, 7 = completely confident). Total scores range from 12 to 84, where higher scores indicate better self-efficacy

Trial sites (1)

FacilityCityRegionStatus
Complejo Hospitalario Universitario Insular Materno Infantil de Gran Canaria Las Palmas de Gran Canaria Las Palmas Recruiting

More Sergio Mies Padilla trials in Spain

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07402642 on ClinicalTrials.gov ↗ ← All trials in Spain