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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 | Clinical Trials | Clareo Health

UNKNOWNNA

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

NCT06107517•National University Hospital, Singapore

View on ClinicalTrials.gov

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) delirium in patients undergoing CABG. The aims of the study are: * Conduct a prospective randomized controlled trial comparing the effectiveness of the DREAMS-OT intervention with standard care in reducing post-CABG delirium in Cardiothoracic Intensive Care Unit (CTICU) * To conduct a nested cost-effectiveness study 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

Age

21 - 99 years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•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

Exclusion Criteria

•Patients who speak other languages are excluded due to the language requirements of certain outcome measures.
•Patients with premorbid severe hearing impairment, severe cognitive impairment, progressive neurological disorders and psychological disorders will be excluded.
•Patients with surgical complications resulting in profuse bleeding from any invasive sites, septic shock unresponsive to maximal treatment, and those who are moribund or have an expected mortality within 48 hours will be excluded.
•Pregnant women will also be excluded from the study as well.
•Patients who develop delirium before initiation of the treatment are also excluded from the study.

Key Dates

Start Date

October 1, 2023

Primary Completion Date

May 1, 2025

Completion Date

August 1, 2025

Last Updated

October 30, 2023

Enrollment

300

ESTIMATED participants

Conditions

Delirium, Postoperative

Interventions

DREAMS-OT

OTHER

Contacts

Lian Ting Wong

CONTACT

+65 6601 3288 lian_ting_wong@nuhs.edu.sg

Seow Zhi Jie

CONTACT

+65 6601 3288 zhi_jie_seow@nuhs.edu.sg

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RECRUITINGNA

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 30, 2023Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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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

Inclusion Criteria

Exclusion Criteria

Effect of Low-dose EsketaMine on dElirium in High-risk Elderly Patients uNdergoing elecTive Surgery (ELEMENT)

Impact of Sleep Quality on Outcomes After Cardiac Surgery

Effect of Percutaneous Acupoint Electrical Stimulation on Delirium

The SCOPE Trial: Sleep, Cognition, and Pain Bundle Vs. ERAS-cardiac for Postoperative Delirium

Effectiveness of Delirium Care Protocol After Cardiac Surgery