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临床试验/KCT0012393
KCT0012393招募中不适用

Early Detection of Patient Deterioration and Determinants of Rapid Response Team Activation Based on Nursing Records

Ajou University0 个研究点目标入组 110 人开始时间: 2026年4月19日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
110

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational
观察模型
Cohort, Time Perspective : Others, Enrollment : 110, Biospecimen Retention : Not collect nor Archive

入排标准

年龄范围
18(Year) 至 No Limit(—)
性别
All

入选标准

  • a. Data analysis
  • Adult patients (=18 years) who were admitted to the general wards at Ajou University Hospital for at least 24 hours between January 1, 2023, and December 31,
  • The RRT activation group will include patients with at least one documented Rapid Response Team (RRT) activation or visit during the study period, whereas the non-activation group will include patients without any documented RRT activation or visit. A total of 100 cases for systematic chart review will be selected from the RRT activation group.
  • b. Focus group interviews
  • Five RRT nurses with at least 5 years of clinical nursing experience, at least 1 year of RRT experience, and experience caring for patients requiring RRT intervention within the past year.
  • Five ward nurses with at least 5 years of clinical nursing experience, at least 1 year of experience in their current ward, and experience caring for patients requiring RRT intervention within the past year.
  • Participants who understand the purpose of the study and voluntarily provide informed consent.
  • Participants who are willing to share and discuss their experiences of caring for patients requiring RRT intervention.

排除标准

  • a. Data analysis
  • The following patients will be excluded from the data analysis:
  • Patients receiving end-of-life or palliative care, identified by palliative care or hospice-related diagnoses or admission to a palliative care unit during hospitalization.
  • Patients with documented Do-Not-Resuscitate (DNR) or Do-Not-Attempt-Resuscitation (DNAR) orders. However, patients whose DNR/DNAR orders were documented after RRT activation will not be excluded.
  • Patients who died within 24 hours of hospital admission.
  • Patients who were admitted exclusively to special care units, such as the intensive care unit, emergency department or operating room.
  • Patients with more than 30% missing data in key variables or whose records could not be reliably identified for analysis.
  • b. Additional exclusion criteria
  • RRT activation group: Patients whose RRT visits were primarily for clinical support services (e.g., assistance with procedures, patient transport, or operation of medical equipment).
  • Non-RRT activation group: Patients who were directly transferred to the ICU or another higher level of care without RRT activation.
  • c. Focus group interviews
  • Participants will be excluded if they:
  • have less than one year of experience working as an RRT nurse or in their current ward.
  • decline or withdraw informed consent.
  • are administrative or non-clinical personnel not directly involved in patient care.

研究者

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