Skip to main content
OpenTrials
Completed

NCT Number: NCT07073872

IDEAL Discharge Education Program

Background: Patients after laparoscopic abdominal surgery are frequently seen with complications such as pain and infection after discharge, which affects the readmission rate of patients to hospital. It is predicted that these complications will be reduced with IDEAL (Include, Discuss, Educate, Assess, and Listen) discharge education given during discharge and patient satisfaction will increase.

Objectives: The aim of this quasi-experimental study was to investigate the effect of discharge education prepared in accordance with IDEAL discharge planning recommendations on discharge satisfaction levels and readmission rates in laparoscopy abdominal surgery patients.

Methods: Patients were recruited from an internationally accredited hospital in Kocaeli, Turkey between February and August 2024. This study was conducted on 62 patients (31 in each intervention and control group). Participants in the intervention group received the nurse-led IDEAL Discharge Education Program (IDEP) and the control group received a standard 15-minute face-to-face discharge education the day of discharge day. The IDEP is a nurse-led, structured discharge education program in accordance with IDEAL Discharge Planning that uses the teach-back method. IDEP is an individualized discharge educational program for surgical patients that utilizes the teach-back method and a printed booklet. Data on discharge education satisfaction was measured at day of discharge (T1), and rehospitalization and readmission was assessed at 1-month after discharge (T2). Outcomes were analyzed with Independent Samples t Test and Chi Square.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Anadolu Medical Center

Kocaeli, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Undergone laparoscopic abdominal surgery
  • Be hospitalized for at least 24 hours
  • Speak and understand Turkish
  • Be 18 years of age or older

Exclusion criteria

  • Have undergone revision surgery
  • Patients with communication difficulties due to any medical condition
  • Patients who refused to participate in the study

Treatment and study plan

IDEAL Discharge Education Program

Other

Participants in the intervention group received the nurse-led IDEAL Discharge Education Program (IDEP) and the control group received a standard 15-minute face-to-face discharge education the day of discharge day. The IDEP is a nurse-led, structured discharge education program in accordance with IDEAL Discharge Planning that uses the teach-back method. IDEP is an individualized discharge educational program for surgical patients that utilizes the teach-back method and a printed booklet.

Control Group

Other

This group receives routine hospital discharge instructions for 15 minutes on the day of discharge.

Primary outcomes

  1. Discharge Education Satisfaction Scale for Surgical Patients

    Time frame: Day 1

    Satisfaction with the discharge education program was assessed using the Discharge Education Satisfaction Scale for Surgical Patients. The scale's scores range from a minimum of 21 to a maximum of 105, with higher scores reflecting greater satisfaction.

  2. Readmission rate

    Time frame: 1st month

    Readmission rate

  3. Rehospitalization rate

    Time frame: 1st month

    Rehospitalization rate

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Collaborators

  • Anadolu Medical Center
  • Kutahya Health Sciences University

Registry information

Official study title

The Effect of Nurse-Led Discharge Education Based on IDEAL Discharge Planning on Discharge Satisfaction and Readmission Rates in Laparoscopic Abdominal Surgery Patients

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jul 18, 2025
Registry last updated
Jul 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.