Tokyo, June 15 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061441) titled 'Feasibility and Implementation of Multidisciplinary Rounds Using a Wellness Checklist in the Intensive Care Unit: A Prospective Quality Improvement Study' on June 15.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - St. Luke's International University

Condition: Condition - Critically ill patients in the Intensive Care Unit (ICU) Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - To implement multidisciplinary care rounds using a novel 4-domain wellness checklist for communicative critically ill patients admitted to the ICU, and to evaluate its feasibility and explore its preliminary effectiveness. Basic objectives2 - Others

Intervention: Interventions/Control_1 - Multidisciplinary care rounds are conducted twice weekly (every Monday and Friday) for communicative critically ill patients in the ICU. A multidisciplinary team consisting of a physician, nurse, pharmacist, dietitian, and physical therapist conducts bedside assessments using a novel 30-item wellness checklist covering 4 domains: physical comfort, environmental comfort, psychological and emotional support, and dignity and communication. Identified discomforts are addressed with immediate on-site interventions by the respective specialists. Outcomes are evaluated by the next-day nurse approximately 24 hours after each round. The intervention period is from June 1, 2026 to December 31, 2026.

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1. Adult patients aged 18 years or older admitted to the ICU of St. Luke's International Hospital. 2. Patients deemed capable of communication (verbal or non-verbal). 3. Patients expected to remain in the ICU for 2 or more days. Key exclusion criteria - 1. Patients under deep sedation (incapable of communication). 2. Patients undergoing emergency procedures or in critical deterioration at the time of rounds. 3. Patients who refuse participation. 4. Patients deemed inappropriate for inclusion by the principal investigator or sub-investigators. Target Size - 80

Recruitment Status: Recruitment status - Enrolling by invitation Date of protocol fixation - 2026 Year 04 Month 30 Day Date of IRB - 2026 Year 06 Month 15 Day Anticipated trial start date - 2026 Year 06 Month 15 Day Last follow-up date - 2026 Year 12 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070299

Disclaimer: Curated by HT Syndication.