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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention VR group | Active Comparator | . 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. |
|
| Standard treatment | Placebo Comparator | Patients in the control group received only standard care. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| VRH (Virtual Reality Hypnosis) | Device | Hypnosis is delivered as a standardized therapeutic intervention through virtual reality, using a digital sedation software (AQUA ®, Onfomfort SA). |
| Measure | Description | Time Frame |
|---|---|---|
| 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. | T1(before intervention) and T3 (directly after intervention) |
| Measure | Description | Time Frame |
|---|---|---|
| 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 | T4 (30 min after intervention) |
| Maternal heart rate |
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Inclusion Criteria:
Exclusion Criteria:
Pregnant woman
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| Name | Affiliation | Role |
|---|---|---|
| Louise Piccart, Dr. | Resident Anesthesiologie | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clinique Saint-Jean | Brussels | 1000 | Belgium |
Publication of abstract (Poster on the ESA 2021) and Study Report (Paper in the Acta Belgica, end of 2021)
end 2021- begin 2022
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 23, 2021 | Aug 18, 2021 | Prot_SAP_000.pdf |
| ICF | No | No | Yes | Informed Consent Form | Nov 20, 2020 | Aug 18, 2021 | ICF_001.pdf |
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| ID | Term |
|---|---|
| D048949 | Labor Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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Prospective interventional Randomized Controlled Trial
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The investigator only gets the anonymized prospective data from the patients
| Standard care | Behavioral | 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. |
|
Measured heart rate during and after intervention as an absolute value.
| T1(before intervention) , T2 (During intervention), T3 (directly after intervention) and T4 (30 min after intervention) |
| Nausea | Nausea and vomiting scores (0-3, 0 = no nausea, 3= nausea and vomiting)) | T1(before intervention) , T3 (directly after intervention) and T4 (30 min after intervention) |
| 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 | T6 (day 1 postpartum) |