Cardiac Rehabilitation in Coronary Artery Diseases

NCT ID: NCT05980364

Last Updated: 2023-08-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 62 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-04-15
• Study Completion Date: 2022-09-15

Brief Summary

Cardiac rehabilitation is approaches that focus on accelerating the recovery process of patients after a cardiac event, improving their physical, psychological and social conditions, and controlling risk factors. Cardiac rehabilitation is known to be an effective and cost-effective approach in the secondary prevention of cardiovascular diseases, most of which are caused by preventable risks. Ischemic heart diseases, one of the cardiovascular diseases, are responsible for 16% of total deaths in the world and have increased significantly since 2000, causing 8.9 million deaths in 2019.

When coronary artery diseases cannot be prevented, the basic approach should be to ensure the individual's compliance with treatment and healthy lifestyle behaviors, and to increase the quality of life and life span.

For this reason, the aim of the study is to examine the effects of technology-based education structured according to the health promotion model in cardiac rehabilitation on healthy lifestyle behaviors, health fatalism and risk knowledge level.

Question 1. Does technology-based education structured according to the health promotion model affect the healthy lifestyle behaviors score? Question 2. Does technology-based education structured according to the health promotion model affect the health fatalism score? Question 3. Does technology-based education structured according to the health promotion model affect the cardiovascular disease risk factors knowledge level score?

Conditions

Have a Diagnosis of Coronary Artery Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: NONE

Study Groups

Experimental group

Group Type: EXPERIMENTAL

Technology-based training structured according to the Health Promotion Model

Intervention Type: OTHER

Experimental group: A video recording was created with a total of 6 zoom applications to be shared with the patients. The content of the video recordings consists of a presentation accompanied by a slide show with open-ended questions prepared by considering the basic concepts of the trainings and the Health Promotion Model. Video recordings, each of which lasted approximately 15-25 minutes, were shared with patients once a week for a total of 6 weeks via WhatsApp. After each video, patients were given three days to watch the video recordings and create their own responses. After this three-day period, the researcher called the patients with whom he shared the content and gave counseling for 10-15 minutes and received feedback. Follow-up was done in the second 6-week period. During the monitoring process, two reminder interviews were made over the phone, with an interval of 2 weeks, for reminder and counseling, and the post-test data were collected at the end of the monitoring period.

Control group

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Technology-based training structured according to the Health Promotion Model

Experimental group: A video recording was created with a total of 6 zoom applications to be shared with the patients. The content of the video recordings consists of a presentation accompanied by a slide show with open-ended questions prepared by considering the basic concepts of the trainings and the Health Promotion Model. Video recordings, each of which lasted approximately 15-25 minutes, were shared with patients once a week for a total of 6 weeks via WhatsApp. After each video, patients were given three days to watch the video recordings and create their own responses. After this three-day period, the researcher called the patients with whom he shared the content and gave counseling for 10-15 minutes and received feedback. Follow-up was done in the second 6-week period. During the monitoring process, two reminder interviews were made over the phone, with an interval of 2 weeks, for reminder and counseling, and the post-test data were collected at the end of the monitoring period.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Having a diagnosis of coronary artery disease (acute coronary syndrome, coronary revascularization, atherosclerotic heart disease, etc.),
• Being stable in health (the patient's health status does not change suddenly and is under control),
• If an interventional procedure has been performed, at least three months have passed after discharge,
• Being between the ages of 18-65,
• Being literate,
• Using smart phone and internet,
• Living in the city center

Exclusion Criteria

• Having a disability (vision, hearing, neurological, cognitive, etc.) that may interfere with education,
• Cardiac rehabilitation is contraindicated
• To have participated in a cardiac rehabilitation program given by another institution before or during the study,

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

Sponsors

Ataturk University

OTHER

Sponsor Role: collaborator

Hatice Karabulak

OTHER

Sponsor Role: lead

Responsible Party

Hatice Karabulak

PhD student

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Prof.Dr.Canturk Capik

Role: STUDY_DIRECTOR

Ataturk University, Department of Public Health Nursing

Locations

Kars Harakani State Hospital

Kars, Merkez, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

02/60

Identifier Type: -

Identifier Source: org_study_id