The Effect of Nurse-led Video-assisted Discharge Training on Anxiety and Readiness for Discharge After Coronary Artery Bypass Graft Surgery

NCT06806631 | Completed

• 1 other identifier: do362957
• Study Type: interventional
• Target: 89
• Locations: 1 country
• Sites: 1

Brief Summary

This clinical trial aims to evaluate the effect of nurse-led video-assisted discharge education on discharge readiness and anxiety in patients undergoing coronary artery bypass graft surgery. The main questions that are aimed to be answered are: Is there a difference between the discharge readiness levels of patients who received video-assisted discharge training and patients who received classical discharge training? Is there a difference between the anxiety levels of patients receiving video-assisted discharge training and patients receiving classical discharge training? Participants: Experimental group Patients in the intervention group were administered the Readiness for Discharge scale and the State Anxiety Scale on the morning of discharge. Afterwards, the discharge training video prepared by the researchers was sent to their cell phones and they were allowed to watch it with the nurse. The researcher also encouraged the patients to ask questions when they did not understand a topic. Since the video remained on the patient's phone, they could watch it again after discharge. After the training, Discharge Readiness Scale and State Anxiety Scale were administered again. Control group On the morning of discharge, patients in the control group were administered the Readiness for Discharge Scale and State Anxiety Inventory. The clinic nurse then gave discharge training, which is a clinical routine. After the training, the Readiness for Discharge Scale and State Anxiety Inventory were administered again.

Conditions

Anxiety; Discharge Readiness; Nursing; Training

Keywords

anxiety; discharge readiness; discharge training; nursing

Outcome Measures

Primary Outcomes (2)

• Anxiety

  State anxiety scale score

  Postoperative 30 day

• Discharge readiness

  Discharge readiness scale score

  Postoperative 30 day

Study Arms (2)

Video assisted discharge training group

EXPERIMENTAL

The researchers developed a training content by utilizing various sources and consulting expert opinions. DISCERN (quality criteria for consumer health information) tool was used to evaluate the information quality of the educational content and 5 expert opinions were obtained and the educational content was finalized in line with the suggestions. The training content included the problems that patients may experience in the postoperative period, postoperative interventions (movement, breathing and cough exercises), control times, nutrition, do's and don'ts and other nursing care issues. The content of the training video prepared according to the DISCERN scale was found to be sufficient. The training content was then converted into a video training given by the nurse researcher.

Other: Video assisted discharge training

Control group

NO INTERVENTION

Patients will receive routine discharge training in the clinic.

Interventions

Video assisted discharge training OTHER

The researchers developed a training content by utilizing various sources and consulting expert opinions. DISCERN (quality criteria for consumer health information) tool was used to evaluate the information quality of the educational content and 5 expert opinions were obtained and the educational content was finalized in line with the suggestions. The training content included the problems that patients may experience in the postoperative period, postoperative interventions (movement, breathing and cough exercises), control times, nutrition, do's and don'ts and other nursing care issues. The content of the training video prepared according to the DISCERN scale was found to be sufficient. The training content was then converted into a video training given by the nurse researcher.

Video assisted discharge training group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• First coronary artery bypass graft surgeryi, good mental health, could speak Turkish

You may not qualify if:

• had hearing or vision problem

Sponsors & Collaborators

• Uskudar University: lead

Study Sites (1)

Hatice Demirdağ

Üsküdar, Istanbul, 34672, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

• HATİCE DEMİRDAĞ

  Üsküdar University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Phd

Model Details: Quasi experimental controlled study

Study Record Dates

• First Submitted: January 22, 2025
• First Posted: February 4, 2025
• Study Start: January 2, 2023
• Primary Completion: October 15, 2023
• Study Completion: October 15, 2023
• Last Updated: February 4, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)