跳至主要内容
临床试验/NCT06983496
NCT06983496招募中不适用

Pharmacist-Intensivist Collaborative Telehealth for Post-Intensive Care Syndrome in Survivors of Critical Illness: a Pilot Randomized Controlled Trial

Malcom Randall VA Medical Center2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2025年6月1日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
24
试验地点
2
主要终点
Completion of Post-ICU follow-up

研究概览

简要总结

The goal of this pilot randomized controlled trial is to determine if a randomized controlled trial of a collaborative pharmacist-intensivist telehealth follow-up after intensive care unit discharge can feasibly be performed in patients who have survived a critical illness.

The study intervention will be telehealth follow-up appointments provided by clinical pharmacists at approximately one and three months post-hospital discharge. The purpose of the follow-up appointments will be to assess for post-intensive care syndrome and provide recommend interventions aimed at improving recovery

Participants will randomized to receive the study intervention or standard of care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults 18-89 years of age
  • Required admission to either medical or surgical ICU
  • Respiratory failure requiring invasive mechanical ventilation of at least 24 hours during ICU stay; or ICU stay of at least 7 days
  • Anticipated discharge to home after hospitalization
  • Consent from patients themselves or a legally authorized representative if necessary

排除标准

  • Pregnancy
  • Incarceration/Imprisonment
  • Life expectancy less than 6 months or enrolled in hospice/palliative care
  • Anticipated discharge to skilled nursing facility, medical rehabilitation facility, or other long terms care facility
  • Unable to participate in telehealth

结局指标

主要结局

Completion of Post-ICU follow-up

时间窗: From enrollment to end of follow-up period at seven months

Percentage of patients completing post-ICU follow-up

次要结局

  • Hospital or ICU re-admissions(Enrollment up to 7 months)
  • Quality of life at 6 months using the Short Form Survey (SF-36)(From enrollment to 7 months)
  • Emergency department visits(Enrollment up to 7 months)
  • Mortality(within 6 months post-hospital discharge)

研究者

申办方类型
Fed
责任方
Principal Investigator
主要研究者

Andrew Franck

Clinical Pharmacy Specialist

Malcom Randall VA Medical Center

研究点 (2)

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