Acute Coronary Syndrome and Nurse Counselling

NCT ID: NCT06034054

Last Updated: 2023-09-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 66 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-01
• Study Completion Date: 2021-07-01

Brief Summary

The goal of this clinical trial is to examine in patients with acute coronary syndrome. The main questions it aims to answer are:

• Does nurse counseling affect quality of life?
• Does nurse counseling affect functional capacity?
• Does nurse counseling affect knowledge, attitudes and beliefs about syndromes?

Participants will be trained using the training booklet, and nursing counseling will then be provided for six months.

If there is a comparison group: Researchers will compare with the control group to see if the nurse counseling has had an effect.

Detailed Description

After obtaining verbal and written consent from the participants, they are required to answer the questions on the Diagnosis Form, Acute Coronary Syndrome Response Index, and Multiple Quality of Life Scale. Then, preliminary measurements will be made and a 6-minute corridor walking test will be applied. While the control group will be followed up routinely, the training booklet prepared for the intervention group will be explained orally. Participants will then be informed that they will be called monthly. They will be told that they can reach these monthly calls and consult the nurse when they need it. After this stage, interviews with patients will begin. The standard way of communication with the participants by the researchers is by telephone, and a total of 6 interviews will be provided, the first of which is in the 1st month after the application of the tests. In each call, all the information in the training booklet will be repeated, additional information will be given in line with the needs and demands of the person, their questions will be answered and the interview will be ended. Although it varies according to the individual interviewed, it is predicted that these telephone interviews will last for 30 minutes on average. Apart from these standard calls, individuals in need will be able to reach the researcher face-to-face during phone calls, text messages, instant messaging methods or hospital visits, and in this way, the counseling process will continue actively for 6 months. After six months, the final tests will be done.

Conditions

Acute Myocardial Infarction; Coronary Artery Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: DOUBLE

Study Groups

Nursing counseling

The individuals included in nursing counseling group were given counseling by the research nurse for 6 months.

Group Type: EXPERIMENTAL

nursing counceling

Intervention Type: OTHER

• Providing an educational booklet containing information about pastry, verbally explaining the content of the prepared educational booklet.
• Answering the information and questions that the patient needs in addition, and receiving contact information in October.
• Monthly calls will be made to patients 6. providing information that the same tests will be performed again per month, if necessary, this monthly call counseling by reaching out without waiting indicating what they can receive.

Control

Individuals included in control group were followed up routinely in the outpatient clinic for 6 months.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

nursing counceling

• Providing an educational booklet containing information about pastry, verbally explaining the content of the prepared educational booklet.
• Answering the information and questions that the patient needs in addition, and receiving contact information in October.
• Monthly calls will be made to patients 6. providing information that the same tests will be performed again per month, if necessary, this monthly call counseling by reaching out without waiting indicating what they can receive.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 18 years old, diagnosed with Acute Coronary Syndrome and treated with a stent,
• Treatment preventing communication is not a problem, literate,
• There is no obstacle to performing the 6-minute walk test.
• who did not accept to participate, were included in the study.

Exclusion Criteria

• <18 years of age,
• Mental or cognitive impairment,
• Diagnosed with SpO2 <80,
• Peripheral arterial disease, lower extremity amputation, impaired tumor or open wound of lower extremity, and deep vein thrombosis, 6 munites corridor Walk test Parts of individuals who are contraindicated in making are not included.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Iskenderun State Hospital

OTHER

Sponsor Role: lead

Responsible Party

Deniz Gülistan ER

Angiography nurse

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

sevgin samancıoğlu bağlama, assoc.prof

Role: STUDY_DIRECTOR

Muğla Sıtkı Koçman University

Locations

İskenderun State Hospital

Hatay, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

DGulistan-01

Identifier Type: -

Identifier Source: org_study_id