Skip to main content
OpenTrials
Completed

NCT Number: NCT07570420

Effect of a Preoperative Video Education Program on ICU Delirium After CABG (VIDEO-CABG Trial)

The goal of this clinical trial is to evaluate the effect of a preoperative video-based educational program on postoperative outcomes in adult patients undergoing coronary artery bypass graft (CABG) surgery.

The main questions it aims to answer are:

Does the video-based educational program reduce the incidence of ICU delirium after CABG surgery? Does the program improve recovery outcomes, including length of ICU stay, hospital stay, and time to early ambulation?

Researchers will compare patients receiving the video-based educational program (intervention group) with those receiving standard care (control group) to determine whether the intervention improves postoperative outcomes.

Participants will:

Be randomly assigned to either the intervention or control group Receive either a structured preoperative video-based education program or standard verbal education Be assessed for ICU delirium using the CAM-ICU tool during ICU stay Have their length of ICU stay and hospital stay recorded from medical records Be monitored for early ambulation within the first 72 hours after surgery

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Jordan

Amman, Amman Governorate, 11118, Jordan

About this study

This randomized controlled trial evaluates the effect of a structured preoperative video-based educational program on postoperative recovery outcomes in adult patients undergoing elective coronary artery bypass graft (CABG) surgery. Postoperative delirium remains a common complication after cardiac surgery and is associated with prolonged intensive care unit (ICU) and hospital stays, delayed recovery, and increased healthcare burden. In addition, delayed mobilization after surgery can further contribute to adverse outcomes.

Traditional preoperative education, typically delivered verbally or through written materials, may be insufficient for patients experiencing stress and anxiety prior to major surgery, leading to poor information retention. Video-based education offers a standardized, accessible, and engaging approach that may enhance patient understanding, improve adherence to recovery protocols, and support better clinical outcomes.

In this study, participants will be randomly assigned to receive either a brief preoperative video-based educational intervention or standard care. The intervention is designed to prepare patients for the postoperative period by providing clear, structured information on recovery expectations, delirium prevention strategies, and the importance of early mobilization.

The primary outcome of interest is the incidence of ICU delirium during the postoperative period. Secondary outcomes include length of ICU stay, length of hospital stay, and timing of early ambulation following surgery. These outcomes will be assessed using standardized clinical measures and hospital records.

By evaluating the effectiveness of a digital educational intervention in a cardiac surgery population, this study aims to contribute evidence on practical, scalable strategies to improve postoperative recovery and reduce complications in patients undergoing CABG surgery.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Participants must meet all of the following criteria:

  • Adult patients aged 18 years or older
  • Scheduled for first-time, elective Coronary Artery Bypass Graft (CABG) surgery
  • Able to read and understand Arabic
  • Admitted preoperatively with sufficient time to receive the intervention (at least 24 hours before surgery)

Exclusion criteria

Participants will be excluded if they meet any of the following criteria:

  • Undergoing emergency or urgent CABG surgery
  • Previous CABG (redo surgery)
  • Cognitive impairment (e.g., diagnosed dementia, severe cognitive deficits, or Alzheimer's disease)
  • Severe communication barriers (e.g., inability to understand Arabic, or severe hearing/visual impairment preventing comprehension of the educational video)
  • Critical preoperative condition that prevents participation in the intervention

Treatment and study plan

Video-Based Educational Program

Behavioral

The video includes:

Overview of CABG surgery and ICU environment Education on ICU delirium (definition, signs, and prevention) Explanation of the ABCDE delirium prevention bundle Instructions on early ambulation and breathing exercises Postoperative recovery expectations

Primary outcomes

  1. Incidence of ICU Delirium

    Time frame: Assessed twice daily (6 AM and 6 PM) during ICU stay, up to discharge from ICU. for three months

    Occurrence of postoperative delirium among patients admitted to the ICU following CABG surgery.

Secondary outcomes

  1. Length of ICU Stay

    Time frame: From ICU admission post-surgery until transfer to ward. for three months

    Duration of time spent in the ICU after surgery.

  2. Length of Hospital Stay (LOS)

    Time frame: From date of surgery until hospital discharge, expected average up to 30 days.

    Hospital length of stay will be calculated from the date and hour of the index CABG surgery until the date and hour of hospital discharge, expressed in days to one decimal place.

  3. Time to First Postoperative Ambulation Within 72 Hours After ICU Admission

    Time frame: From ICU admission (postoperative day 0) through 72 hours after surgery.

    Time to first walk will be measured in hours from ICU admission after CABG surgery (T0) until the start of the first qualifying walking episode. Transfers from bed to chair will not be counted as ambulation. If no walking occurs within 72 hours, it will be recorded as "72+" with the clinical reason documented.

Sponsors and collaborators

Lead sponsor

University of Jordan

Other

Collaborators

  • Jordanian Royal Medical Services

Registry information

Official study title

The Effect of Preoperative Video-Based Educational Program on Patient's Incidence of ICU Delirium, Length of Stay, and Ambulation Post Coronary Artery Bypass Graft Surgery. A Randomized Controlled Trial

Acronym: VIDEO-CABG

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 6, 2026
Registry last updated
May 6, 2026

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.