Virtual Reality in Labor and Delivery for Reduction in Pain
NCT03437031 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2021-11-26
Summary
The purpose of this study is to identify whether use of virtual reality devices can improve the pain management of women in labor and delivery. The investigators will perform a randomized controlled trial of patients in labor at Cedars-Sinai Medical Center.
Conditions
- Labor Pain
- Virtual Reality
- Alternative Medicine
Interventions
- DEVICE
-
Virtual Reality device
For those patients randomized to VR, the study staff member will explain the use of the Samsung VR goggle set, and thereafter will allow the patient to use the device freely for up to 30 minutes. Intervals of 2-5 minutes is suggested for first-time use, and patients will be to allowed to discontinue it at any time as long as they are not experiencing any discomfort or side effects (dizziness, motion sickness, etc.). The study staff member will be present at all times, and will work with hospital staff as necessary to ensure the patient is receiving appropriate clinical care throughout the duration of the intervention.
Sponsors & Collaborators
-
Cedars-Sinai Medical Center
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-03-01
- Primary Completion
- 2019-02-19
- Completion
- 2019-02-19
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
A Comparison Study Of Two Different Techniques For Identifying The Epidural Space In Parturients In Labour
NCT01574391 ·Status: COMPLETED ·Phase: NA
-
Comparison of Epidural Labor Pain Relief Techniques on Maternal and Fetal Outcomes
NCT02008591 ·Status: COMPLETED ·Phase: PHASE4
-
Optimal Regimen of Patient-controlled Epidural Analgesia in Laboring Patients
NCT03566342 ·Status: TERMINATED
-
Evaluation of the Effect the Medical Team in the Delivery Room Has on Pain Management During Labor.
NCT03045705 ·Status: WITHDRAWN ·Phase: NA
-
The Impact of Virtual Doula Services on Birth Outcomes in Rural Communities
NCT07293741 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
The Effects of Labor Stages and Interventions on Hemodynamic Measures During & After Childbirth With Noninvasive Sensors
NCT03838965 ·Status: COMPLETED ·Phase: NA
-
Semi-permanent Acupuncture Effect on Cervical Ripening
NCT06357962 ·Status: TERMINATED ·Phase: NA
-
Inertial Sensors for Obstetrical Walking Epidural Tracking
NCT06471790 ·Status: RECRUITING
-
Induction to Labour With Double Cervical Ballon at Home Versus at Hospital
NCT06053073 ·Status: RECRUITING ·Phase: NA
-
A Clinical Phase II Study of the Materna Device to Shorten Delivery Time During Childbirth
NCT06698185 ·Status: WITHDRAWN ·Phase: NA
-
3D Ultrasound-guided Labor Epidural Analgesia in the Morbid Obese Parturient
NCT03405311 ·Status: TERMINATED ·Phase: NA
-
Induction of Labor in Patients With Unfavorable Cervical Conditions
NCT00604487 ·Status: COMPLETED ·Phase: NA
-
Comparison of Loss of Resistance Techniques
NCT00638274 ·Status: COMPLETED ·Phase: PHASE2
-
Visual Aids for Induction of Labor RCT
NCT05671224 ·Status: COMPLETED ·Phase: NA
-
Study to Determine if Monitoring of Labor Shortens the Time to Delivery
NCT01005667 ·Status: WITHDRAWN ·Phase: NA
-
Optimizing Management of the 2nd Stage of Labor: Multicenter Randomized Trial
NCT02137200 ·Status: TERMINATED ·Phase: NA
-
Testing the Efficiency of a Device Meant to Relieve Labour Pain
NCT00426725 ·Status: COMPLETED ·Phase: NA
-
Noninvasive Monitoring of Uterine Activity and Fetal Heart Rate
NCT05782296 ·Status: COMPLETED
-
VPIA Remifentanil for Labour Pain to Reduce Maternal Desaturation and Improve Analgesic Titration
NCT02733835 ·Status: UNKNOWN ·Phase: PHASE4
-
Nitrous Oxide and Neuraxial Labor Analgesia Use on Maternal Fetal Outcomes
NCT04813874 ·Status: WITHDRAWN
-
Neuraxial Versus Systemic Analgesia for Latent Phase Labor Effect on Rate of Operative Delivery
NCT00380978 ·Status: COMPLETED ·Phase: NA
-
Cervical Volume by Three-Dimensional Ultrasound as a Predictor of Preterm Delivery
NCT00342550 ·Status: COMPLETED
-
Evaluation of Objective Pain Measurement Device
NCT03975660 ·Status: COMPLETED ·Phase: NA
-
Prelabor Visual Biofeedback by a Self-operated Ultrasound Device
NCT06049784 ·Status: RECRUITING ·Phase: NA
-
Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix
NCT03752073 ·Status: TERMINATED ·Phase: NA