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临床试验/NCT05183412
NCT05183412已完成不适用

Effect of Virtual Reality (VR) Therapy on Patients Undergoing Hand Surgery Under Ultrasound-guided Regional Anesthesia: a Randomized Controlled Superiority Trial.

Jessa Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2022年1月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120
试验地点
1
主要终点
Pain due to the placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)

研究概览

简要总结

By means of an investigator-initiated, monocentric, single-blinded, prospective, randomized controlled superiority trial, the effect of virtual reality (VR) therapy on patients undergoing ambulatory hand surgery under ultrasound-guided regional nerve block will be investigated. It is hypothesized that the usage of VR during the placement of the nerve block in ambulatory hand surgery patients provides a significant decrease in pain score during anesthesia compared to without VR glasses. Additionally, an objective stress related parameter (HRV), anxiety, VR experience (immersion and presence), adverse effects and patient satisfaction are evaluated before anesthesia, during anesthesia and surgery or after surgery through validated questionnaires or measurements.

详细描述

Ultrasound-guided regional anesthesia (RA) is the golden standard in ambulatory superficial hand surgery due to its safety and reliability. Frequently used RA techniques are ultrasound-guided distal peripheral nerve block of the n. medianus and n. ulnaris is and ultrasound-guided axillary nerve block of the n. medianus, n. ulnaris, n. radialis, and n. musculocutaneous. The needling is frequently accompanied by stress, fear or anxiety and it has been proven in studies that psychological factors can affect the sensation of pain. At this moment systemic opioids and/or sedatives used, however, these partially neutralize the benefits of locoregional techniques.

Virtual reality (VR) is a non-pharmacologic and non-invasive simulation in which the user can interact within a 3D-computer-generated environment using special glasses with a screen and a headset. VR offers the ability to distract patients from reality and can therefore relieve a pain sensation from harmful stimuli. An important aspect of pain reduction in VR is presence and immersion. The physical/sensory stimulus offered by the artificial environment is referred to as immersion. Presence can be defined as one's sense of being in an artificial environment. The VR glasses of the firm Oncomfort called Sedakit™ have been proven to be safe and effective in previous clinical trials. A VR program namely 'Aqua', has been provided and designed for relaxation and distraction from anxiety or pain of patients.

Current literature is lacking objective parameters of stress within an operative, anesthesiologic framework. One of these objective stress-related parameters of is heart rate variability (HRV). HRV is the fluctuation of the length between consecutive heart beats and refers to the heart's ability to react to a wide range of physiological and environmental stimuli such as stress. HRV can be measured by the Empatica E4 wristband.

The proposed study, performed at the Jessa hospital, will assess the effect of VR glasses on pain levels of hand surgery patients during placement of the nerve block and surgery by comparing a group with VR glasses to without VR glasses. It is hypothesized that the usage of VR during the placement of the nerve block in ambulatory hand surgery patients provides a significant decrease in pain score during anesthesia compared to without VR glasses. Additionally, an objective stress related parameter (HRV), anxiety, VR experience (immersion and presence), adverse effects and patient satisfaction are evaluated before anesthesia, during anesthesia and surgery or after surgery through validated questionnaires or measurements.

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)

盲法说明

Two independent assessors will gather data in this study: one blinded and one unblinded.

入排标准

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

入选标准

  • ≥18 years and <65 years
  • ASA (American Society of Anesthesiology) classification: 1 - 3
  • Patient scheduled for ambulatory hand surgery using ultrasound-guided axillary block regional anesthesia or ultrasound-guided peripheral nerve block.

排除标准

  • Bilateral surgery
  • BMI ≥ 40 kg/m²
  • Motion sickness
  • Patient that take medication that affects heart rhythm (beta-blockade)
  • Infection in the area for peripheral nerve block injections.
  • Existing neurological conditions.
  • Chronic pain symptoms
  • Opioid use within the past 3 months
  • Allergy to local anesthetics
  • Inability to experience the VR glasses experience (Vision disorders)
  • Inability to understand study design or mental impairment
  • Patients with autonomic nervous system dysfunction
  • Pregnancy
  • Heart transplant patients, patients with diabetic neuropathy, patients with myocardial infarction (or having passed through it) and/or tetraplegic patients
  • Fear of being under water
  • Sea sickness

结局指标

主要结局

Pain due to the placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)

时间窗: Procedure (At the end of performing the ultrasound-guided regional anesthesia block)

Pain caused by performing the anesthesia technique (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)

次要结局

  • Surgical time(During surgery)
  • Patient satisfaction (7-point Likert scale)(Intraoperative (At the end of surgery))
  • Pain due to the surgery: Numeric Rating Scale (NRS)(Intraoperative (At the end of surgery))
  • Stress: Heart rate variability (HRV)(Before performing the ultrasound-guided regional anesthesia block for 5 minutes in rest (baseline), procedure (during performing the ultrasound-guided regional anesthesia block ) and minute 0 - 5 during the surgical procedure.)
  • Anxiety due to placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)(Procedure (At the end of performing the ultrasound-guided regional anesthesia block))
  • Anxiety due to the surgery: Numeric Rating Scale (NRS): Numeric Rating Scale (NRS)(Intraoperative (At the end of surgery))
  • Pre-surgical anxiety (Surgical Fear Questionnaire)(Arrival at the 1 day clinic)
  • VR experience: Immersion and presence (Igroup questionnaire)(Intraoperative (At the end of surgery))
  • Adverse effects (Simulation Sickness Questionnaire and Virtual Reality Symptom Questionnaire)(Intraoperative (At the end of surgery))
  • Opiod use peroperatively(Intraoperative (At the end of surgery))
  • Needling time(Procedure (During performing the ultrasound-guided regional anesthesia block))

研究者

发起方
Jessa Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stessel Björn

Principle Investigator

Jessa Hospital

研究点 (1)

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