Actively Recruiting
Reducing Delirium After CABG Surgery With Early Activation and Sleep-Promoting Routines
Led by National University Hospital, Singapore · Updated on 2026-03-30
300
Participants Needed
1
Research Sites
133 weeks
Total Duration
On this page
Sponsors
N
National University Hospital, Singapore
Lead Sponsor
N
National University of Singapore
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this randomized-controlled trial (RCT) is to compare the effectiveness of the DREAMS-OT intervention with standard care in reducing post-Coronary Artery Bypass Graft (CABG) surgery delirium in patients undergoing CABG surgery. The aims of the study are: 1. To determine if early and intensive OT will lower the incidence of post-op delirium in CABG patients compared to standard are. 2. To determine the cost effectiveness of the DREAMS-OT intervention. The study team will compare intervention group and standard care group (control group) to see if there is a reduction in the incidence of delirium in patients 5 days post-CABG.
CONDITIONS
Official Title
Reducing Delirium After CABG Surgery With Early Activation and Sleep-Promoting Routines
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients deemed medically suitable for elective CABG surgery
- Patients aged 21 years and above
- Patients who are English or Mandarin speaking
- Patients who are able to provide consent
You will not qualify if you...
- Patients who speak other languages due to language requirements of outcome measures
- Patients with premorbid severe hearing impairment, severe cognitive impairment, progressive neurological disorders, or psychological disorders
- Patients with surgical complications causing profuse bleeding from invasive sites, septic shock unresponsive to treatment, or expected mortality within 48 hours
- Pregnant women
- Patients who develop delirium before starting treatment
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
National University Hospital
Singapore, Singapore, 119074
Actively Recruiting
Research Team
M
Megan HL Tan
CONTACT
M
Michell KS Low
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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