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Effect of Virtual Reality (VR) Therapy on Patients Undergoing Hand Surgery Under Ultrasound-guided Regional Anesthesia

Primary Purpose

Anesthesia, Local, Surgery, Hand Injuries

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
The Sedakit Oncomfort VR glasses (30-minutes Aqua program)
Ultrasound-guided regional nerve block and hand surgery without VR glasses
Ultrasound-guided regional nerve block and hand surgery with VR glasses
Sponsored by
Jessa Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Anesthesia, Local focused on measuring Virtual reality glasses, Heart rate variability

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥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.

Exclusion Criteria:

  • 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

Sites / Locations

  • Jessa hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Ultrasound-guided regional nerve block and hand surgery without VR glasses

Ultrasound-guided regional nerve block and hand surgery with VR glasses

Arm Description

Patients will not receive the VR glasses during the ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery.

Patients will receive the VR glasses during the ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Pain due to the surgery: Numeric Rating Scale (NRS)
Pain caused by performing the hand surgery (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Stress: Heart rate variability (HRV)
Heart rate variability (HRV), is the fluctuation of the length between consecutive heart beats in milliseconds and is regulated by the autonomic nerve system. It determines the balance between the parasympathetic 'rest and digest' and sympathetic 'flight or fight' nerve systems. The sympathetic branch decreases HRV during stressful situations, while the parasympathetic branch increases HRV at rest. This natural interplay between the two systems allows the heart to quickly respond to different stimuli, including stress. HRV (being RMSSD and HF-HRV), is measured during placement of an ultrasound-guided regional anesthesia block and surgery through the Empatica E4 wristband (Photoplethysmography).
Anxiety due to placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)
Anxiety caused by performing the anesthesia technique (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Anxiety due to the surgery: Numeric Rating Scale (NRS): Numeric Rating Scale (NRS)
Anxiety caused by performing the hand surgery (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Pre-surgical anxiety (Surgical Fear Questionnaire)
Pre-surgical anxiety for the anesthesia and surgery (measured with the Surgical Fear Questionnaire)
VR experience: Immersion and presence (Igroup questionnaire)
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.
Adverse effects (Simulation Sickness Questionnaire and Virtual Reality Symptom Questionnaire)
Adverse effects (dizziness, headache, motion sickness, postoperative nausea and vomiting, fatigue, claustrophobia) are evaluated by the virtual reality symptom questionnaire (VRSQ) and Simulator sickness questionnaire (SSQ).
Opiod use peroperatively
Rescue medication in case of block failure.
Patient satisfaction (7-point Likert scale)
Patient satisfaction measured with the Patient Satisfaction Questionnaire and a 7-point Likert scale for measuring satisfaction rates with anesthesia, surgery and VR experience.
Needling time
The time from injection of the needle to the removal of the needle.
Surgical time
The time from incision to surgical completion

Full Information

First Posted
January 5, 2022
Last Updated
September 19, 2023
Sponsor
Jessa Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05183412
Brief Title
Effect of Virtual Reality (VR) Therapy on Patients Undergoing Hand Surgery Under Ultrasound-guided Regional Anesthesia
Official Title
Effect of Virtual Reality (VR) Therapy on Patients Undergoing Hand Surgery Under Ultrasound-guided Regional Anesthesia: A Randomized Controlled Superiority Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 26, 2022 (Actual)
Primary Completion Date
August 6, 2023 (Actual)
Study Completion Date
August 6, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jessa Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anesthesia, Local, Surgery, Hand Injuries
Keywords
Virtual reality glasses, Heart rate variability

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Two independent assessors will gather data in this study: one blinded and one unblinded.
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ultrasound-guided regional nerve block and hand surgery without VR glasses
Arm Type
Active Comparator
Arm Description
Patients will not receive the VR glasses during the ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery.
Arm Title
Ultrasound-guided regional nerve block and hand surgery with VR glasses
Arm Type
Experimental
Arm Description
Patients will receive the VR glasses during the ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery.
Intervention Type
Device
Intervention Name(s)
The Sedakit Oncomfort VR glasses (30-minutes Aqua program)
Intervention Description
During placement of ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery, patients are subjected to a 30-minutes VR program (Oncomfort SA, Wavre, Belgium) 'Aqua' via a head-mounted display and headphone. The patients watch a VR underwater view of the ocean while listening to speeches to induce relaxation and meditation.
Intervention Type
Procedure
Intervention Name(s)
Ultrasound-guided regional nerve block and hand surgery without VR glasses
Intervention Description
During placement of ultrasound-guided regional nerve block (axillary or distal peripheral) and hand surgery, patients are NOT subjected to a 30-minutes VR program (Oncomfort SA, Wavre, Belgium) 'Aqua' via a head-mounted display and headphone.
Intervention Type
Procedure
Intervention Name(s)
Ultrasound-guided regional nerve block and hand surgery with VR glasses
Intervention Description
Ultrasound-guided regional nerve block and hand surgery with VR glasses
Primary Outcome Measure Information:
Title
Pain due to the placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)
Description
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)
Time Frame
Procedure (At the end of performing the ultrasound-guided regional anesthesia block)
Secondary Outcome Measure Information:
Title
Pain due to the surgery: Numeric Rating Scale (NRS)
Description
Pain caused by performing the hand surgery (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Time Frame
Intraoperative (At the end of surgery)
Title
Stress: Heart rate variability (HRV)
Description
Heart rate variability (HRV), is the fluctuation of the length between consecutive heart beats in milliseconds and is regulated by the autonomic nerve system. It determines the balance between the parasympathetic 'rest and digest' and sympathetic 'flight or fight' nerve systems. The sympathetic branch decreases HRV during stressful situations, while the parasympathetic branch increases HRV at rest. This natural interplay between the two systems allows the heart to quickly respond to different stimuli, including stress. HRV (being RMSSD and HF-HRV), is measured during placement of an ultrasound-guided regional anesthesia block and surgery through the Empatica E4 wristband (Photoplethysmography).
Time Frame
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.
Title
Anxiety due to placement of the ultrasound-guided regional anesthesia block: Numeric Rating Scale (NRS)
Description
Anxiety caused by performing the anesthesia technique (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Time Frame
Procedure (At the end of performing the ultrasound-guided regional anesthesia block)
Title
Anxiety due to the surgery: Numeric Rating Scale (NRS): Numeric Rating Scale (NRS)
Description
Anxiety caused by performing the hand surgery (measured via an 11-point Numeric Rating Scale where 0 = no pain and 10 is worst pain imaginable)
Time Frame
Intraoperative (At the end of surgery)
Title
Pre-surgical anxiety (Surgical Fear Questionnaire)
Description
Pre-surgical anxiety for the anesthesia and surgery (measured with the Surgical Fear Questionnaire)
Time Frame
Arrival at the 1 day clinic
Title
VR experience: Immersion and presence (Igroup questionnaire)
Description
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.
Time Frame
Intraoperative (At the end of surgery)
Title
Adverse effects (Simulation Sickness Questionnaire and Virtual Reality Symptom Questionnaire)
Description
Adverse effects (dizziness, headache, motion sickness, postoperative nausea and vomiting, fatigue, claustrophobia) are evaluated by the virtual reality symptom questionnaire (VRSQ) and Simulator sickness questionnaire (SSQ).
Time Frame
Intraoperative (At the end of surgery)
Title
Opiod use peroperatively
Description
Rescue medication in case of block failure.
Time Frame
Intraoperative (At the end of surgery)
Title
Patient satisfaction (7-point Likert scale)
Description
Patient satisfaction measured with the Patient Satisfaction Questionnaire and a 7-point Likert scale for measuring satisfaction rates with anesthesia, surgery and VR experience.
Time Frame
Intraoperative (At the end of surgery)
Title
Needling time
Description
The time from injection of the needle to the removal of the needle.
Time Frame
Procedure (During performing the ultrasound-guided regional anesthesia block)
Title
Surgical time
Description
The time from incision to surgical completion
Time Frame
During surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥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. Exclusion Criteria: 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
Facility Information:
Facility Name
Jessa hospital
City
Hasselt
State/Province
Limburg
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effect of Virtual Reality (VR) Therapy on Patients Undergoing Hand Surgery Under Ultrasound-guided Regional Anesthesia

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