None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient: (1) Aged >=18 years; (2) Mechanical ventilation time >=24h, ICU admission >=24h; (3) The patient's Sedation score at Richmond Agitation-Sedation Scale (RASS) was >=-3 points (meeting the criteria for delirium evaluation); (4) Informed consent to participate in this study. 2. Family members: (1) Aged >=18 years; (2) Informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: 1. Patient: (1) Inability to communicate with researchers (visual or hearing impairment); (2) Patients with extensive burns and skin defects; (3) Primary nerve injury (patients with severe craniocerebral injury and subarachnoid hemorrhage); (4) GCS score < 9; (5) Three no personnel. 2. Family members: Unable to communicate with researchers (visual and hearing impairments).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of delirium; | — |
Secondary
| Measure | Time frame |
|---|---|
| Delirium duration;Time and amount of delirium drugs used;Delirium-related adverse outcomes; | — |
Countries
China
Contacts
Huazhong University of Science and Technology Union Shenzhen Hospital