Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:48 PM
Ignite Modification Date:
2025-12-24 @ 10:48 PM
NCT ID:
NCT02926469
Eligibility Criteria:
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
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02926469
Study Brief:
Protocol Section:
NCT02926469