Virtual Reality in Labor and Delivery for Reduction in Pain
Status: | Recruiting |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/2/2019 |
Start Date: | March 1, 2018 |
End Date: | August 1, 2019 |
Contact: | Melissa S Wong, MD |
Email: | Melissa.Wong2@cshs.org |
Phone: | 310-423-0895 |
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.
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.
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 hypothesize that use of
virtual reality devices will result in a reduction in pain medication use, in epidural use,
and prolong the duration of time prior to the patient receiving an epidural.
The study will be conducted as two parallel randomized controlled trials: one for latent
labor patients and one for patients in active labor (defined by whether they are < 6 cm or >
6 cm). Within each phase of labor, there will be 20 in the Virtual Reality arm and 20 in the
Control arm for a total of 80 patients.
the pain management of women in labor and delivery. The investigators hypothesize that use of
virtual reality devices will result in a reduction in pain medication use, in epidural use,
and prolong the duration of time prior to the patient receiving an epidural.
The study will be conducted as two parallel randomized controlled trials: one for latent
labor patients and one for patients in active labor (defined by whether they are < 6 cm or >
6 cm). Within each phase of labor, there will be 20 in the Virtual Reality arm and 20 in the
Control arm for a total of 80 patients.
Inclusion Criteria:
1. Female
2. >18 years old
3. Pregnant with term gestation
4. Nullipara
5. Pain due to contractions rated from 4-7
6. Contractions at least every 5 minutes x 30 minutes preceding
7. Pain scores obtained at least every 60 minutes
Exclusion Criteria:
1. Parous
2. Use of intravenous medications for pain relief prior to the intervention
3. Use of an epidural
4. Preterm gestation
5. Pain not due to contractions
6. Pain score of 3 or below or 8 or above
We found this trial at
1
site
8700 Beverly Blvd # 8211
Los Angeles, California 90048
Los Angeles, California 90048
(1-800-233-2771)
Principal Investigator: Kimberly D Gregory, MD MPH
Phone: 310-423-0895
Cedars Sinai Med Ctr Cedars-Sinai is known for providing the highest quality patient care. Our...
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