Skip to content

Co-design and application of an ICU electronic diary platform: a mixed-method study

Co-design and application of an ICU electronic diary platform: a mixed-method study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079903
Enrollment
Unknown
Registered
2024-01-16
Start date
2024-01-20
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Post-traumatic stress disorder

Interventions

control group:The control group received routine nursing mode, including creating a comfortable environment for patients
Pay attention to the pain response of patients and take timely intervention
Actively communicate with patients and their families
The nutritional status of patients was evaluated and the diet nursing was done well. Individualized rehabilitation programs were developed for patients.
Intervention Group 1:On the basis of routine nursing mode, ICU electronic diary platform was applied, and the diary was issued on the day of the subjects' transfer from ICU.
Intervention Group 2:On the basis of routine nursing mode, ICU electronic diary platform was applied, and the diary was issued 30 days after the subjects were transferred out of ICU.

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Age =18 years old; ? first ICU admission; ? ICU stay time =48 hours; ? Tracheal intubation time =24 hours; ? All patients and their family members voluntarily participated in this study with informed consent.

Exclusion criteria

Exclusion criteria: ? previous history of mental illness; (2) those who died during the study or were discharged voluntarily; ? patients with severe visual and hearing impairment and unable to communicate; (4) those who are participating in other research projects; And 5) patients with a history of psychotropic drug addiction or psychoactive substance abuse.

Design outcomes

Primary

MeasureTime frame
Incidence of post-traumatic stress disorder;

Secondary

MeasureTime frame
Anxiety and depression;sleep quality;

Countries

China

Contacts

Public ContactHU RUJUN

Affiliated Hospital of Zunyi Medical University

hurujunok@163.com+86 150 8506 0545

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026