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Clinical Trials/NCT06174090
NCT06174090
Recruiting
Not Applicable

The Effect of Patient Education With Video Prior to Coronary Artery Bypass Graft Surgery on Pain, Anxiety and Knowledge Levels of Patients

Baskent University1 site in 1 country46 target enrollmentStarted: September 5, 2023Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
46
Locations
1
Primary Endpoint
Pain Level

Overview

Brief Summary

The aim of this research to examine the effectiveness of video-education on pain, anxiety, and knowledge levels on adult patients undergoing coronary artery bypass graft surgery.

Detailed Description

A video based patient education will be used in this randomized controlled study. Patient education via video aims to reduce the patient's anxiety levels, control their pain, and improve their health outcomes by increasing knowledge levels. In addition, since this training is visual-based, it is aimed to provide effective learning by reducing the inequality due to sociodemographic and individual differences between participants. The video-education includes information about pre and post-surgical process and care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Outcomes Assessor)

Masking Description

Double

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Being at least 18 years old
  • Being hospitalized in Cardiovascular Surgery Clinic and Cardiovascular surgery intensive care unit
  • Undergoing coronary artery bypass graft surgery for the first time, by sternotomy method
  • Patients who agree to participate in the research and read and sign the "Informed Volunteer Consent Form for Scientific Research"

Exclusion Criteria

  • Patients with visual or hearing impariment
  • Patients with psychiatric illness,
  • Patients with known cognitive impairment (dementia, Alzheimer's).

Outcomes

Primary Outcomes

Pain Level

Time Frame: from 24th of surgery to 72nd hour

Visual analog scale (VAS): VAS is a widely used scale for pain assessment. The scale was developed by Albersnagel, and its validity and reliability in our country were established by Aydin et al. In VAS, pain averages ranging from 0 to 10 are given on a 10 cm scale. Accordingly, while "0" indicates no pain, an average VAS value of "1-4" indicates mild pain, "5-6" indicates moderate pain, and "7-10" indicates severe. Change= VAS score of video-education group\<standard verbal education.on 24th, 48th, and 72nd hours after surgery

Anxiety level

Time Frame: from baseline prior to education to 72nd hour of surgery

State anxiety scale (STAI-I): The scale determines how the individual feels at a certain moment, in a certain condition, and his/her emotions regarding the situation. The total score obtained from the scale is between 20-80. A high score indicates a high level of anxiety. The feelings and behaviors expressed in the State Anxiety Scale items are answered by marking one of the following conditions, such as (1) not at all, (2) a little, (3) a lot and (4) completely, according to the severity of such experiences. Change= STAI-I score of video-education group\<standard verbal education.on pre-and-post education, and on 72nd hours after surgery.

Preoperative anxiety

Time Frame: from baseline prior to education to 72nd hour of surgery

Amsterdam Preoperative Anxiety and Information Scale (APAIS): The scale is one of the scales used to evaluate preoperative anxiety. Source of anxiety; It is divided into three: due to surgery, anesthesia or lack of information. It contains 6 statements regarding these three sources to assess anxiety. In order to objectify the survey, each statement is given a numerical value based on a 5-point Likert scale according to severity; These values, ranging from 1 to 5; 1=none, 2=mild, 3=moderate, 4=severe, 5=extreme severity. Higher score means higher preoperative anxiety. Change= APAIS score of video-education group\<standard verbal education n pre-and-post education, and on 72nd hours after surgery.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gulcin Sahin

RN, MSc

Baskent University

Study Sites (1)

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