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临床试验/NCT05180552
NCT05180552撤回不适用

The HEALiX Trial: Comparing the Efficacy of the HEALiX Device With Wrist Restraints in a Critical Care Setting

Milton S. Hershey Medical Center0 个研究点目标入组 100 人开始时间: 2028年8月10日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
100
主要终点
Unplanned removal of devices

研究概览

简要总结

The treatment plan for patients requiring mechanical ventilator support is to provide the minimal amount of analgesics and sedatives necessary for the patient to tolerate the ventilator as lower amounts of these drugs has been shown to improve patient outcomes. Patients in this critical state experience confusion, restlessness, and agitation, which sometimes leads to an unplanned removal of a patient's line or medical device. The current standard of care for limiting the movement of mechanically ventilated patients' in the critical care units in hospitals is the use of physical wrist restraints. Researchers demonstrated that wrist restraints are ineffective in preventing the removal of invasive and adjunct devices and have many negative physical, psychological, physiological, and emotional consequences for the patient and their family. In this proposed research, we will use the innovative medical device called the HEALiX, a newly developed device worn on the arms of mechanically ventilated patients that allows freedom of movement and protects from removing adjunct mechanical ventilation devices and invasive monitoring equipment. This randomized controlled trial will investigate the HEALiX device's effectiveness in preventing the removal of invasive monitoring devices (such as endotracheal tubes, central lines, feeding tubes, etc.) compared with the current standard of care, wrist restraints.

详细描述

This randomized controlled trial's primary purpose is to determine the efficacy of the HEALiX compared with wrist restraints in the adult, intubated patient in the critical care and intermediate care setting. The study's secondary purpose is to understand the acceptability of the HEALiX from healthcare professionals' perspective providing care at the bedside. By recruiting participants for use in the HEALiX RCT study and using the HEALiX with patients during care, the PI will gather information regarding the comparative effectiveness of the HEALiX in a population of critical care patients. This RCT trial will use a quantitative, comparative approach using an experimental and control study group design to measure and compare the outcomes after the subjects are placed in either the HEALiX or wrist restraints.

The setting for the HEALiX Pilot Study will be Penn State Hershey Medical Center in Hershey Pennsylvania. The specific location for the trial will be in several of the academic medical center's critical care units, including Heart and Vascular ICU (HVICU), Surgical Anesthesia ICU (SICU), Neurosurgical Intensive Care Unit (NSICU), and Medical Intensive Care Unit (MICU). Key nursing unit leaders and leaders from other service lines whose clinical input was essential to contribute to this RCT trial's success gave permission to conduct this study.

研究设计

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

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Mechanically ventilated (with or without tracheostomy)
  • Receiving analgesic-sedating medications
  • Wearing soft wrist restraints
  • Glasgow Coma Scale score > 8
  • Participants must be between ages 18-89 years old
  • English-speaking
  • English speaking legalized authorized representative (LAR)
  • Participants must be admitted under one of the following physician groups: Trauma services or critical care physician group.

排除标准

  • Children (under age 18)
  • Pregnant women
  • Cognitively impaired adults (must be able to follow commands)
  • Combative patients

结局指标

主要结局

Unplanned removal of devices

时间窗: End of intubation (average 7 days)

Frequency of unplanned removal of lines and self-extubation

次要结局

  • Days on the ventilator that each patient group remains(End of intubation (average 7 days))
  • Number of days in the ICU that each patient group remains(End of ICU stay when patient is transferred to lower level of care (average 10 days))
  • Midazolam Dosing(1 Day)
  • Propofol Dosing(1 Day)
  • Ease of device use(End of intubation (average 7 days))
  • Fentanyl Dosing(1 Day)

研究者

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

Eliessa Caplan

Eliessa Caplan, BS, MSN, DNP, RN, CCRN Principal Investigator

Milton S. Hershey Medical Center

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