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Clinical application of post-ICU syndrome prevention program in patients based on enriched environment theory

Construction and preliminary application of early post-ICU syndrome prevention program in patients based on enriched environment theory

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076798
Enrollment
Unknown
Registered
2023-10-18
Start date
2023-10-19
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

post-intensive care syndrome

Interventions

Intervention group:1.Preparation Build a team. A Set up a multidisciplinary team led by ICU specialist nurses with the participation of ICU doctors, respiratory therapists, rehabilitation therapists,
for patients who cannot express but have motor function and observable behavior, the Intensive Care Pain Observation tool (CPOT) should be used
depth of sedation should be evaluated using the Richmond agitation and sedation score. B Follow the principle of priority analgesia and minimal shallow sedation to control NRS<4 points or CPOT<3 marks
Shallow sedation (RASS-2 to 1) was performed for patients without markers of deep sedation, and d

Sponsors

School of Nursing, Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: ? Patients admitted to ICU with clear consciousness. ? Age =18 years old. ? The Barthel index score of the patient was =75 points 2 weeks before ICU admission. ? First admission to ICU. ? Participate voluntarily and sign informed consent.

Exclusion criteria

Exclusion criteria: ?Length of ICU stay < 7 days. ? Previous physical, cognitive, mental, visual, hearing impairment. ? Can not cooperate with the intervention and scale test. ? Diseases that may affect the results of the study, such as severe brain trauma, acute nervous system damage events (such as cerebrovascular accidents, subarachnoid hemorrhage, etc.). (5) People who quit during the study.

Design outcomes

Primary

MeasureTime frame
Barthel Index;Pittsburgh Sleep Quality Index;Mini-Mental StateExamination;Hospital Anxiety and Depression Scale;Impact of events scale-revised;

Secondary

MeasureTime frame
Medical Research Council muscle strength score;Confusion assessment method for the Intensive Care Unit; Length of ICU stay;

Countries

China

Contacts

Public ContactHu Shaohua

School of Nursing, Anhui Medical University

paper2390@163.com+86 139 0969 6207

Outcome results

None listed

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