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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

TypeNameDescription
OTHERDREAMS-OTPatients 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.

Reducing Delirium After CABG Surgery With Early Activation and Sleep-Promoting Routines (NCT06107517) · Clinical Trials Directory