IDEAL Discharge Education Program
The Effect of Nurse-Led Discharge Education Based on IDEAL Discharge Planning on Discharge Satisfaction and Readmission Rates in Laparoscopic Abdominal Surgery Patients
1 other identifier
interventional
62
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 12, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 8, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 8, 2024
CompletedFirst Submitted
Initial submission to the registry
June 27, 2025
CompletedFirst Posted
Study publicly available on registry
July 18, 2025
CompletedJuly 18, 2025
July 1, 2025
6 months
June 27, 2025
July 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Discharge Education Satisfaction Scale for Surgical Patients
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.
Day 1
Readmission rate
Readmission rate
1st month
Rehospitalization rate
Rehospitalization rate
1st month
Study Arms (2)
IDEAL Discharge Education Program (IDEP)
EXPERIMENTALIDEAL Discharge Education Program (IDEP)
Control Group
ACTIVE COMPARATORcontrol group
Interventions
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.
This group receives routine hospital discharge instructions for 15 minutes on the day of discharge.
Eligibility Criteria
You may qualify if:
- Undergone laparoscopic abdominal surgery
- Be hospitalized for at least 24 hours
- Speak and understand Turkish
- Be 18 years of age or older
You may not qualify if:
- Have undergone revision surgery
- Patients with communication difficulties due to any medical condition
- Patients who refused to participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Kocaeli Universitylead
- Kutahya Health Sciences Universitycollaborator
- Anadolu Medical Centercollaborator
Study Sites (1)
Anadolu Medical Center
Kocaeli, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Inversigator
Study Record Dates
First Submitted
June 27, 2025
First Posted
July 18, 2025
Study Start
February 12, 2024
Primary Completion
August 8, 2024
Study Completion
September 8, 2024
Last Updated
July 18, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share