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Virtual Reality Analgesia in Labor: The VRAIL Pilot Study

Virtual Reality Analgesia in Labor: The VRAIL Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02926469
Acronym
VRAIL
Enrollment
28
Registered
2016-10-06
Start date
2016-10-25
Completion date
2017-04-14
Last updated
2018-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor Pain

Keywords

Virtual Reality, Analgesia, Immersive Virtual Reality, VR, Labor, Pain

Brief summary

The purpose of the proposed study is to evaluate the feasibility of using immersive Virtual Reality (VR) during labor. We will also explore whether VR distraction is helpful for reducing subjective pain during labor, even if this pain is severe or excruciating. We predict that VR is feasible in this setting and that VR distraction will reduce acute pain and anxiety during labor.

Detailed description

This study used an over the counter consumer product to create a virtual reality experience so that we could assess whether there was a decrease in perception of pain.

Interventions

DEVICEVirtual Reality

Using Virtual Reality during labor

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Any woman giving birth for the first time at or after 32 weeks * Low risk pregnancy without obstetric complications * In first stage of labor for vaginal delivery * Desires non-pharmacologic alternative for pain control

Exclusion criteria

* Younger than 18 or older than 45 years of age * Presence of fetal or placental anomaly * High risk pregnancy or anesthetic concerns (BMI\>40, difficult airway, hemorrhage, nonreassuring FHR, malpresentation) * Current use of pharmacologic analgesia including neuraxial anesthesia * Not capable of answering study measures using numeric rating scale * Any face/head/neck injuries that interfere with the use of Virtual Reality equipment * Any form of contact precautions * Severe hearing or vision deficits * Susceptibility to motion sickness * Seizure history * History of psychiatric disorder, chronic pain, migraines, or addiction * Delirium, psychosis, any form of developmental delay, or Organic Brain Disorder * Requiring an interpreter for communication

Design outcomes

Primary

MeasureTime frameDescription
Pain and Anxietyone time for the duration of one minute after 10 minutes of contractions with standard carePain is measured one time after 10 minutes of contractions with standard care, by asking the subjects about their pain and anxiety level, using a questionnaire called graphic rating scale.
Satisfactionone time for the duration of one minute after using Virtual RealityEvaluate women's attitudes towards Virtual Reality use during labor through a satisfaction questionnaire.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026