None listed
Conditions
Interventions
Intervention group:On top of routine non-pharmacological delirium management, receive a 5-day multisensory intervention program.
Control group:Routine non-pharmacological delirium management
Sponsors
The Second People's Hospital of Wuxi
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patient Inclusion Criteria (1) Age>= 18 years old; (2) Expected ICU admission >= 72 hours; (3) Richmond Agitation-Sedation Scale (RASS) sedation score >=-3 points (eligible for delirium assessment); (4) Glasgow Coma Score> 9 points; (5) Informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: (1) Have severe hearing impairment or visual impairment and are unable to communicate with researchers; (2) Patients with extensive burns and skin defects; (3) Diagnosed with dementia, delirium, or acute mental illness at the time of admission; (4) History of alcohol abuse or psychotropic substance abuse before admission to ICU; (5) It has been added to other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of delirium; | — |
Secondary
| Measure | Time frame |
|---|---|
| Delirium duration;Sleep quality;Cognitive function;Length of ICU stay; | — |
Countries
China
Contacts
Public ContactBian hong
The Second People's Hospital of Wuxi
Outcome results
None listed