Heart Bypass Surgery Clinical Trials

Clinical trials related to Heart Bypass Surgery Procedure

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
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Maximum Age: 99
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Singapore
National University Hospital
RECRUITING
Singapore
Contact Information
Primary
Megan HL Tan
megan_huei_lin_tan@nuhs.edu.sg
+65-96280613
Backup
Michell KS Low
michell_kai_sian_low@nuhs.edu.sg
+65 83164092
Time Frame
Start Date: 2024-01-08
Estimated Completion Date: 2026-08
Participants
Target number of participants: 300
Treatments
Experimental: DREAMS-OT Arm (Intervention Group)
Patients will receive an early and intensive occupational therapy protocol starting within the first 15 hours after extubation.
No_intervention: Standard Care Arm (Control Group)
Standard care OT as per current ICU setting
Sponsors
Collaborators: National University of Singapore, National Medical Research Council (NMRC), Singapore
Leads: National University Hospital, Singapore

This content was sourced from clinicaltrials.gov