Effect of the Education Given to the Patients Who Will Be Applied Coronary Angiography

NCT ID: NCT05160935

Last Updated: 2022-08-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 79 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-01
• Study Completion Date: 2022-07-30

Brief Summary

This research; The aim of this study was to evaluate the effect of the pre-procedural education given to the patients undergoing coronary angiography on the anxiety level and vital signs of the patients.

Detailed Description

Coronary Artery Disease is a vascular disease in the category of atherosclerosis, which is characterized by complete or partial occlusion of the arteries, providing oxygen-rich blood to meet the metabolic needs of the heart. It was shown as the top 10 causes of death worldwide in 2017 by the World Health Organization. According to the 2018 data of the Turkish Statistical Institute (TUIK), it has been reported that 39.7% of the deaths caused by the circulatory system in Turkey are due to heart diseases. Coronary angiography, which is among the diagnostic methods of coronary artery disease; It is the process of evaluating the coronary arteries by making them visible by administering radiopaque material to the femoral, brachial, radial and axillary arteries during cardiac catheterization. One of the basic roles of nursing is to provide education for the recovery of the individual and the maintenance of health. In this context, it is thought that nurses' caring about the role of educator in patient care will contribute to reducing the patient's anxiety.

Research; This study was planned to evaluate the effect of pre-procedural education on patients undergoing coronary angiography on their anxiety level and vital signs.

The research was planned as a quasi-experimental study with pretest-posttest control group design between November 2021 and June 2022. The population of all patients who underwent coronary angiography in the Cardiology Service of Eskişehir City Hospital, the sample was calculated using the G-Powr 3.1 program and it was found appropriate to include 79 people in each group with a 95% CI 90% power. The "Simple Randomization Method" will be used to divide the individuals who agree to participate in the research into the experimental and control groups. Since the individuals in the sample group will share the same environment, the experimental group will be included in data collection on even days and the control group on odd days. A "Diagnostic Form" will be filled in for all patients in the sample, their vital signs will be evaluated, and the "State-Trait Anxiety Inventory" will be administered. For the patients in the experimental group; Before the coronary angiography procedure, training will be given by using the "Training Booklet" prepared by the researchers in line with the literature and the opinion of the specialist physician. After the coronary angiography procedure, the "State-Trait Anxiety Inventory" will be re-administered to the patients and their vital signs will be followed. In the control group; Before the coronary angiography procedure, verbal information will be given for the coronary angiography procedure within the scope of the routine procedure in the clinic, in line with the information in the patient consent form. After the procedure, the State-Trait Anxiety Inventory will be applied again. Vital signs will be monitored. The obtained data will be evaluated with appropriate statistical methods.

As a result of the research, it is thought that the questions of whether the education given to the patients who will undergo coronary angiography have an effect on reducing the anxiety levels of the patients and have a positive effect on the vital signs values will be answered.

Keywords: Coronary angiography, anxiety, vital signs, education, nursing, nursing care

This research; The aim of this study was to evaluate the effect of the pre-procedural education given to the patients undergoing coronary angiography on the anxiety level and vital signs of the patients.

Research Questions;

• Does the training given to the patients who will undergo coronary angiography have an effect on the anxiety level of the patients?
• Does the training given to the patients who will undergo coronary angiography have a positive effect on the vital signs of the patients?

Conditions

Coronary Angiography; Anxiety; Vital Signs; Education; Nursing; Nursing Care

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: NONE

Study Groups

Coronary Angiography Training Manual

It is the form prepared by the researchers in line with the literature information and the opinion of the specialist physician was taken. It contains information about coronary artery disease, what to do before coronary angiography procedure and what kind of situations await individuals after the procedure.

Group Type: EXPERIMENTAL

Education

Intervention Type: BEHAVIORAL

Each patient will be informed about the study, and written consent will be obtained from patients who agree to participate in the study, explaining the purpose and duration of the study. A Patient Identification Form will be filled, the patient's vital signs will be evaluated, and the State-Trait Anxiety Inventory will be administered to the patient.

Before the coronary angiography procedure, the patients in the experimental group will be trained by the researchers using the training booklet. Trait Anxiety Inventory will be re-administered to the patients after the procedure. Vital signs of patients will be monitored.

In the control group; In line with the information in the patient consent form before the coronary angiography procedure, verbal information will be given about the coronary angiography procedure within the scope of the routine procedure in the clinic. After the procedure, the State-Trait Anxiety Inventory will be applied again. Vital signs will be taken.

Interventions

Education

Each patient will be informed about the study, and written consent will be obtained from patients who agree to participate in the study, explaining the purpose and duration of the study. A Patient Identification Form will be filled, the patient's vital signs will be evaluated, and the State-Trait Anxiety Inventory will be administered to the patient.

Before the coronary angiography procedure, the patients in the experimental group will be trained by the researchers using the training booklet. Trait Anxiety Inventory will be re-administered to the patients after the procedure. Vital signs of patients will be monitored.

In the control group; In line with the information in the patient consent form before the coronary angiography procedure, verbal information will be given about the coronary angiography procedure within the scope of the routine procedure in the clinic. After the procedure, the State-Trait Anxiety Inventory will be applied again. Vital signs will be taken.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Having at least literate education level,
• 18 years old or older,
• No communication problems,
• Does not have mental or psychiatric disease,
• Agreeing to participate in the study voluntarily,
• Individuals who will undergo coronary angiography for the first time.

Exclusion Criteria

• Being illiterate
• Being under the age of 18
• Having any communication problem,
• Having mental or psychiatric disease,
• Not wanting to participate in the study,
• Individuals who have undergone coronary angiography before.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Eskisehir Osmangazi University

OTHER

Sponsor Role: lead

Responsible Party

Sevil PAMUK CEBECİ

Asst.Prof.Dr.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sevil PAMUK CEBECİ

Role: STUDY_DIRECTOR

sevil.pamukcebeci@ogu.edu.tr

Locations

Eskişehir Şehir Hastanesi

Eskişehir, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

2021-1

Identifier Type: -

Identifier Source: org_study_id