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Discrete Choice Experiment of ICU Delirium Prevention and Management Bundle: The Minimum Viable Component Set and Implementation Stratification Strategy under Resource Constraints

Discrete Choice Experiment of ICU Delirium Prevention and Management Bundle: The Minimum Viable Component Set and Implementation Stratification Strategy under Resource Constraints

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124281
Enrollment
Unknown
Registered
2026-05-09
Start date
2026-05-09
Completion date
Unknown
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium

Interventions

Observation group:None

Sponsors

The Second Hospital,University of South China
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Registered nurses engaged in direct bedside nursing in general ICU or specialized ICU. 2.Having worked continuously in the current department for no less than 6 months, with a stable understanding of the hospital’s delirium management protocols and actual workload. 3.Having knowledge of or participated in at least partial relevant practices, including delirium screening, sedation management, early mobilization, sleep promotion, and orientation support. 4.Volunteers who participate in the study, sign electronic or written informed consent, and are capable of completing questionnaires independently.

Exclusion criteria

Exclusion criteria: 1.Nurses only undertaking administrative, teaching or research work without frontline bedside nursing duties. 2.Student nurses, those with excessively short rotation periods, or those who have not yet mastered the delirium management protocols of their department. 3.Participants who fail to complete core discrete choice experiment (DCE) questions, present obviously illogical responses, submit questionnaires repeatedly, or fail the attention check. 4.Other participants deemed ineligible for data analysis by the researchers.

Design outcomes

Primary

MeasureTime frame
Target Event Probability;

Countries

China

Contacts

Public ContactYixingke, Fengxiuchan

The Second Hospital,University of South China

18570909816@163.com+86 734 889 9708

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026