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临床试验/NCT04622527
NCT04622527已完成不适用

Acceptability of Virtual Reality Experience by Health Care Providers for Improving Focus and Reducing Anxiety: A Pilot Trial

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
24
试验地点
1
主要终点
State-Trait Anxiety Inventory (STAI Y1)

研究概览

简要总结

The purpose of this study is to evaluate the acceptability of using Virtual Reality intervention to help reduce anxiety and burnout symptoms and improve focus in the workplace.

详细描述

The proposed investigation will apply two novel paradigms using proprietary Virtual Reality interventions designed to reduce anxiety and inattention. We will explore whether this intervention is safe and acceptable, and whether it can impact the stress, anxiety, and difficulty in focus of employees in the workplace. Participants will view two different nature videos in two different formats. Each video will be experienced through Virtual Reality or non- Virtual Reality.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Single (Participant)

盲法说明

Virtual Reality headgear and corresponding non-Virtual Reality are pre-programmed with paradigms. Participants were unaware of the order of the experience they will view.

入排标准

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

入选标准

  • •18 years of age or older at the time of consent.
  • •Healthcare Professional with the Mayo Clinic.
  • •Not pregnant by participant self-report at time of consent.
  • •Have the ability to provide informed consent.
  • •Have no contraindicated comorbid health conditions as determined by the clinical investigators.

排除标准

  • •Currently (within the past 3 weeks) practicing mindfulness training on a weekly/regular basis.
  • •Currently (within the past 3 weeks) undergoing an additional program (e.g., Complementary and Alternative Medicine [CAM]) to improve quality of life.
  • •Currently (within 3 weeks) enrolled in another clinical or research program (e.g., CAM) which impacts the patients' quality of life (QOL), stress or anxiety.
  • •Currently has photosensitivity.
  • •Cannot tolerate virtual reality experiences.
  • •An unstable medical or mental health condition as determined by the physician investigator (e.g., pre-existing eye strain, seizures, dizziness, nausea)

研究组 & 干预措施

A = Virtual Reality paradigm A

Active Comparator

Begin with Paradigm A virtual reality headgear

干预措施: Random assigned paradigm viewing order (Other)

B = Virtual Reality paradigm B

Active Comparator

Begin with Paradigm B virtual reality headgear

干预措施: Random assigned paradigm viewing order (Other)

C = Non-Virtual Reality paradigm A

Sham Comparator

Begin with Paradigm A without virtual reality headgear

干预措施: Random assigned paradigm viewing order (Other)

D = Non-Virtual Reality paradigm B

Sham Comparator

Begin with Paradigm B without virtual reality headgear

干预措施: Random assigned paradigm viewing order (Other)

结局指标

主要结局

State-Trait Anxiety Inventory (STAI Y1)

时间窗: 2 weeks

STAI Y1 anxiety measurement of the change from post-test score to pre-test score. The STAI Y1 has 20 questions on a scale from 1 to 4. The minimum score is 20 and the maximum is 80. The lower the score the better the outcome. Our outcome looks at the difference between the post-test from the pre-test, so the minimum change score is -60 and the maximum change score is 60. A higher change in score would mean that a subject experienced a worse outcome after the paradigm, while a lower change in score shows a better outcome after the paradigm than before.

次要结局

  • Was the Study Worthwhile(2 weeks)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ivana T Croghan, PhD

Principal Investigator

Mayo Clinic

研究点 (1)

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