Application of a flexible visitation system in critically ill patients: a randomized clinical trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200059093

Enrollment

Unknown

Registered

2022-04-24

Start date

2022-04-10

Completion date

Unknown

Last updated

2024-02-11

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

Conditions

delirium

Interventions

the experimental group:flexible visitation

Eligibility

Sex/Gender

All

Age

14 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included patients who had consecutive admissions and admission times > 24 h.

Exclusion criteria

Exclusion criteria: The exclusion criteria were as follows: delirium occurring at ICU admission; persistent coma during ICU hospitalization; and the inability to complete the CAM-ICU scoring.

Design outcomes

Primary

Measure	Time frame
whether delirium occurred;	—

Secondary

Measure	Time frame
whether a nosocomial infection occurred;whether complaints occurred;the satisfaction questionnaire;ICU length of stay;length of hospital stay;	—

Countries

China

Contacts

Public ContactFang Feng

Lanzhou University Second Hospital

ldyy_fengf@lzu.edu.cn+869318942844

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026