Trials / Recruiting
RecruitingNCT06107517
Reducing Delirium After CABG Surgery With Early Activation and Sleep-Promoting Routines
DREAMS-OT Trial: Delirium Reduction Through Early Activation in Motivating and Sleep Promoting Routines: A Randomized Controlled Trial of Occupational Therapy for ICU Patients After Coronary Artery Bypass Graft (CABG) Surgery
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- Sponsor
- National University Hospital, Singapore · Academic / Other
- Sex
- All
- Age
- 21 Years – 99 Years
- Healthy volunteers
- Not accepted
Summary
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
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | DREAMS-OT | Patients will receive the DREAMS-OT protocol 3 times per day, 20 minutes per therapy session. Intervention frequency will be confirmed with a feasibility trial. If not feasible to maintain 3 times per day, the intervention will still be maintained at the same intensity of 1 hour per day, with a graded approach. |
Timeline
- Start date
- 2024-01-08
- Primary completion
- 2026-08-01
- Completion
- 2026-08-01
- First posted
- 2023-10-30
- Last updated
- 2026-03-30
Locations
1 site across 1 country: Singapore
Source: ClinicalTrials.gov record NCT06107517. Inclusion in this directory is not an endorsement.