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Virtual Reality to Reduce Labor Pain (VRH4L)

Primary Purpose

Labor Pain, Virtual Reality, Hypnosis

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
VRH (Virtual Reality Hypnosis)
Standard care
Sponsored by
Clinique Saint-Jean, Bruxelles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Labor Pain focused on measuring non-pharmacological analgesia

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age: ≥ 18 and ≤ 45 years
  2. Pregnant with term gestation
  3. Willing to adhere to the rules linked to the use of the VRH headset: turning off mobile phone, visit bathroom in advance, no new visitors and no interference of the partner other than when the woman would ask him so
  4. Provision of written informed consent
  5. Induced labor

Exclusion Criteria:

  1. Complicated pregnancy ( HELLP,…)
  2. Scheduled caesarian delivery
  3. Receipt of epidural analgesia or opioid painkillers before start active labor phase
  4. Low auditory acuity that precludes use of the device
  5. Low visual acuity that precludes use of the device
  6. Head or face wounds precluding use of the device
  7. Schizophrenia
  8. Epilepsy
  9. Dizziness
  10. Non-proficiency in French and/or Dutch (research language)

Sites / Locations

  • Clinique Saint-Jean

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Intervention VR group

Standard treatment

Arm Description

. In the VRH group the patients received a 30-minute session of virtual reality hypnosis when in active labor and had access to standard care.

Patients in the control group received only standard care.

Outcomes

Primary Outcome Measures

Post interventional pain scores
Primary outcome was the difference in post intervention pain score between the two arms. Difference in Numerical Rating Scale (0 to 10, where 0 is no pain and 10 is maximum pain) pain scores after the intervention between the VRH and Standard care group.

Secondary Outcome Measures

Pain 30 minutes after intervention
Measure of Numerical Rating Scale (0 to 10, where 0 is no pain and 10 is maximum pain) after 30 minutes
Maternal heart rate
Measured heart rate during and after intervention as an absolute value.
Nausea
Nausea and vomiting scores (0-3, 0 = no nausea, 3= nausea and vomiting))
Satisfaction of the mother
Likert scale (-2,0,2) .-2 is very dissatisfied, 1= dissatisfied, 0= not satisfied, nor dissatisfied, 1= satisfied and 2 is very satisfied

Full Information

First Posted
November 6, 2021
Last Updated
January 3, 2022
Sponsor
Clinique Saint-Jean, Bruxelles
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1. Study Identification

Unique Protocol Identification Number
NCT05167383
Brief Title
Virtual Reality to Reduce Labor Pain
Acronym
VRH4L
Official Title
A Prospective Randomized Controlled Monocentric Study Evaluating the Impact of Virtual Reality Hypnosis During Labor
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
May 30, 2021 (Actual)
Study Completion Date
May 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clinique Saint-Jean, Bruxelles

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
Background and Goal of Study Labor pain remains an area where different analgesia options are looked for, more specifically non-pharmacological remedies are popular. Hypnosis and virtual reality (VR) have been studied with encouraging results. However, until now, the combination of VR and hypnosis (VRH) has not been assessed during labor, although it has shown promising results in other acute pain areas. The VRH4L study will evaluate the efficacy of Virtual Reality Hypnosis (VRH) in reducing pain during labor. Hypnosis is delivered as a standardized therapeutic intervention through virtual reality, using a digital sedation software (AQUA ®, Oncomfort SA). For this prospective, interventional parallel group, monocentric randomized controlled trial full term women who were planned for an induction of labor at the St-Jean Hospital in Brussels from March to May 2021 were included. Women with complicated pregnancies and patients with contraindications to VR were excluded. Patients were randomized in two arms. In the VRH group the patients received a 30-minute session of virtual reality hypnosis when in active labor and had access to standard care. Patients in the control group received only standard care. Primary outcome was the difference in post intervention pain score between the two arms. Secondary outcomes were the difference in pain score 30 minutes after the intervention, vital signs correlated to pain, satisfaction of the experience, interaction with the midwife and prevalence of side effects. Data was analyzed using the student's T test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Labor Pain, Virtual Reality, Hypnosis
Keywords
non-pharmacological analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective interventional Randomized Controlled Trial
Masking
Investigator
Masking Description
The investigator only gets the anonymized prospective data from the patients
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention VR group
Arm Type
Active Comparator
Arm Description
. In the VRH group the patients received a 30-minute session of virtual reality hypnosis when in active labor and had access to standard care.
Arm Title
Standard treatment
Arm Type
Placebo Comparator
Arm Description
Patients in the control group received only standard care.
Intervention Type
Device
Intervention Name(s)
VRH (Virtual Reality Hypnosis)
Intervention Description
Hypnosis is delivered as a standardized therapeutic intervention through virtual reality, using a digital sedation software (AQUA ®, Onfomfort SA).
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
The standard treatment (ST) for labor pain as used in our hospital contains massage, aquatherapy and postural exercises. This is always available for any woman in labor.
Primary Outcome Measure Information:
Title
Post interventional pain scores
Description
Primary outcome was the difference in post intervention pain score between the two arms. Difference in Numerical Rating Scale (0 to 10, where 0 is no pain and 10 is maximum pain) pain scores after the intervention between the VRH and Standard care group.
Time Frame
T1(before intervention) and T3 (directly after intervention)
Secondary Outcome Measure Information:
Title
Pain 30 minutes after intervention
Description
Measure of Numerical Rating Scale (0 to 10, where 0 is no pain and 10 is maximum pain) after 30 minutes
Time Frame
T4 (30 min after intervention)
Title
Maternal heart rate
Description
Measured heart rate during and after intervention as an absolute value.
Time Frame
T1(before intervention) , T2 (During intervention), T3 (directly after intervention) and T4 (30 min after intervention)
Title
Nausea
Description
Nausea and vomiting scores (0-3, 0 = no nausea, 3= nausea and vomiting))
Time Frame
T1(before intervention) , T3 (directly after intervention) and T4 (30 min after intervention)
Title
Satisfaction of the mother
Description
Likert scale (-2,0,2) .-2 is very dissatisfied, 1= dissatisfied, 0= not satisfied, nor dissatisfied, 1= satisfied and 2 is very satisfied
Time Frame
T6 (day 1 postpartum)

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant woman
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: ≥ 18 and ≤ 45 years Pregnant with term gestation Willing to adhere to the rules linked to the use of the VRH headset: turning off mobile phone, visit bathroom in advance, no new visitors and no interference of the partner other than when the woman would ask him so Provision of written informed consent Induced labor Exclusion Criteria: Complicated pregnancy ( HELLP,…) Scheduled caesarian delivery Receipt of epidural analgesia or opioid painkillers before start active labor phase Low auditory acuity that precludes use of the device Low visual acuity that precludes use of the device Head or face wounds precluding use of the device Schizophrenia Epilepsy Dizziness Non-proficiency in French and/or Dutch (research language)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louise Piccart, Dr.
Organizational Affiliation
Resident Anesthesiologie
Official's Role
Study Chair
Facility Information:
Facility Name
Clinique Saint-Jean
City
Brussel
ZIP/Postal Code
1000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Publication of abstract (Poster on the ESA 2021) and Study Report (Paper in the Acta Belgica, end of 2021)
IPD Sharing Time Frame
end 2021- begin 2022

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Virtual Reality to Reduce Labor Pain

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