跳至主要内容
临床试验/NCT03621228
NCT03621228Unknown不适用

A Pilot Study of an Interactive Digital Technology (MindfulGarden) in Treatment of Hyperactive Delirium in a Hospital Setting

Simon Fraser University0 个研究点目标入组 24 人开始时间: 2018年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
24
主要终点
Recruitment Rates

研究概览

简要总结

This pilot study is designed to address feasibility for a larger randomized control clinical study that will determine the efficacy of exposure to the MindfulGarden - an interactive digital technology - in reducing hyperactive delirium in hospitalized older adults.

详细描述

The primary objective of the study is to establish whether the key components necessary for conducting a full randomized control study in the future, such as recruitment, consent, randomization, and treatment processes are working well and all function together. As a secondary objective, the investigators will determine trends in patients exposed to MindfulGarden (MG), for example:

  1. At the first and second administration of the Confusion Assessment Method - short form (CAM) after admission to a medical ward are there more, the same or fewer patients in the intervention group than in the control group whose CAM scores change from positive to negative?
  2. During the first 24 hours after admission to a medical ward, did fewer, the same, or a greater number of patients in the intervention than in the control group experience significant events/alerts (e.g. aggressive/violent behaviours, falls, code white)?
  3. During the first 24 hours after admission to a medical ward, were fewer, the same, or a greater number of patients in the intervention than in the control group administered psychotropic drugs (e.g. haloperidol, risperidone, quetiapine, lorazepam)? were more, the same, or fewer administered sleeping aids (e.g. trazodone, melatonin)?
  4. During the first 24 hours after admission to a medical ward, were fewer, the same, or a greater number of patients in the intervention than in the control group physically restrained?
  5. Was mean length of stay from time of admission to a medical ward until discharge due to death, return to place of residence before admission or to a different place of residence longer, the same or shorter in the intervention than in the control group?
  6. Were there more, the same or fewer deaths or discharges to a higher level of care (e.g. to assisted living, to a complex care facility in patients who previously lived at home) in the intervention than the control group?

Additionally, to the extent that movement and vocalization are reflective of anxiety, agitation and/or aggression (i.e. responsive behaviours) the investigators also want to determine whether there is a correlation between changes in these as recorded by the MG and any of the indicators listed in 1-6 above.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients aged 65 years or older admitted to the Emergency Department who have a diagnosis of hyperactive delirium as defined by the short CAM

排除标准

  • Patients with severe vision impairment or who are legally blind
  • Patients for whom a bed in a medical ward was not available within 12 hours of a diagnosis of hyperactive delirium (i.e. who remained in the Emergency Department more than 12 hours)

研究组 & 干预措施

MindfulGarden

Experimental

Standard care + exposure to an interactive digital device

干预措施: MindfulGarden (Device)

Control

No Intervention

Standard care only

结局指标

主要结局

Recruitment Rates

时间窗: Number enrolled within 12 hours of admission to Emergency Department

Number of participants approached and their rate of consent

次要结局

  • Estimate the potential effect size(24-hour period following transfer from Emergency Department)
  • Adverse Outcomes (number of patients with aggressive/violent behaviours, falls, code white)(24-hour period following transfer from Emergency Department)
  • Length of Stay(Date of study enrolment through to discharge from hospital, or date of study enrolment up to 30 days)
  • Psychotropic Drug Consumption(24-hour period following transfer from Emergency Department)
  • Application of Physical Restraints(24-hour period following transfer from Emergency Department)

研究者

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

Gloria Gutman

Professor Emerita

Simon Fraser University

相似试验