Title | Immersive virtual reality analgesia in un-medicated laboring women (during stage 1 and 2): a randomized controlled trial | The Effect of Virtual Reality on Pain in Primiparity Women | The effect of cognitive behavioral techniques using virtual reality on birth pain: a randomized controlled trial | Virtual Reality Reduces Pain in Laboring Women: A Randomized Controlled Trial | The Effect of Showing Images of the Foetus with the Virtual Reality Glass During Labour Process on Labour Pain, Birth Perception and Anxiety | Comparison of the effectiveness of virtual reality and chewing mint gum on labor pain and anxiety: a randomized controlled trial | Virtual Reality, Fear of Pain and Labor Pain Intensity: A Randomized Controlled Trial | Immersive virtual reality on childbirth experience for women: a randomized controlled trial | Virtual reality is beneficial in decreasing pain in labouring women: A preliminary study | Virtual Reality Analgesia in Labor: The VRAIL Pilot Study—A Preliminary Randomized Controlled Trial Suggesting Benefit of Immersive Virtual Reality Analgesia in Unmedicated Laboring Women |
Authors | Narges Momenyan, Ali Asghar Safaei, Sedighe Hantoushzadeh | Intan Gumilang Pratiw, Farid Husin, Ahmad Rizal Ganiem, Hadi Susiarno, Achmad Arifin, Firman Wirahkusuma | Elif Yagmur Gür, Serap Ejder Apay | Melissa S. Wong, MD, MHDS, Brennan M.R. Spiegel, MD, MSHS, Kimberly D. Gregory, MD, MPH | Bihter Akin, Mine Yilmaz Kocak, Zehra Küçükaydın, Kübra Güzel | Atefeh Ebrahimian, Roghaieh Rahmani Bilandi, Mohammad Reza Rahmani Bilandi, Zahra Sabzeh | Halimeh Mohammadi, Javad Rasti, Elham Ebrahimi | Elif Gizem Carus, Nazli Albayrak, Halit Mert Bildirici, Selen Gur Ozmen | Lorna Massov, Brian Robinson, Edgar Rodriguez-Ramirez, Robyn Maude | David P. Frey, DO, Melissa E. Bauer, DO, Carrie L. Bell, MD, Lisa Kane Low, PhD, CNM, Afton L. Hassett, PsyD, Ruth B. Cassidy, MA, Katherine D. Boyer, BS, Sam R. Sharar, MD |
Year of publication | 2021 | 2017 | 2020 | 2020 | 2021 | 2022 | 2023 | 2022 | 2023 | 2019 |
Country of study | Iran | Indonesia | Turkey | United States | Turkey | Iran | Iran | Turkey | New Zealand | United States |
Study design | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial | Randomized controlled trial with Cross-over | Randomized controlled trial with Cross-over |
Sample size | 52 | 60 | 273 | 40 | 100 (50 intervention group, 50 control group) | 93 (31 in each group) | 130 | 42 (21 in each group) | 14 | 28 (27 completed) |
Inclusion criteria | Healthy Iranian women, age 18–45, first-time giving birth after 38 weeks, no desire for pharmacologic pain intervention, low-risk pregnancy, anticipated vaginal delivery | Indonesian national, low risk of pregnancy without obstetric complication, came to health public services on latent phase | Not having visual or auditory impairment, admitted to the delivery room for vaginal delivery, term pregnancy (38–40 weeks), active phase of labor (5–7 cm dilatation), no obstetric risks, not receiving oxytocin, carrying a live fetus | Nulliparous, term women in labor with pain scores of 4 to 7, having regular contractions at least every 5 minutes, ≥ 18 years old, English-speaking, able to give informed consent | In the 28th week of pregnancy, primiparous, head presentation, no risks regarding the pregnant woman and foetus, over the age of 18, agreed to participate in the study | Consent to participate, gravida 1 or 2, singleton pregnancy, live embryo, active phase of childbirth, maternal age 18–35 years, pregnancy stage 37–41 weeks, no medical or mental illness, no abnormal embryos, cephalic presentations, low risk pregnancy | Healthy pregnant women, 37–41 weeks gestation, singleton pregnancy, vertex presentation, no chronic medical conditions or pregnancy complications | Women between 18–42 years of age, 37–41 weeks gestation, singleton pregnancy, vertex presentation, no history of chronic medical conditions, no pregnancy complications | Women at ≥ 35 weeks gestation, nulliparous or multiparous in active first stage of labour, pain score > 8, three contractions in ten minutes lasting 60–90 seconds | Healthy women at ≥ 32 weeks’ gestation giving birth for the first time, in the first stage of labor with anticipated vaginal delivery |
Exclusion criteria | High-risk pregnancy, need for other analgesia methods, fetal or placental anomaly, inability to assess pain, hearing or vision impairment, mental disorders, seizure history, motion sickness predisposition, undesirable VR content memory | Parturient rejects the VR intervention, came in active phase of labor before intervention, did not receive complete intervention, obstetric complication | Visual or auditory impairment, not meeting other inclusion criteria, refusal to participate | Use of any medications for pain relief prior to intervention, preterm gestation, pain not due to contractions, pain scores outside of the intended range, risk for seizures, sensitivity to flashing light/motion, medical condition predisposing to nausea/dizziness, injury to eyes/face/neck or arms | Elective caesarean, got pregnant with assisted reproductive techniques, vision and hearing problems, decided to go into labor in another institution, emergency cesarean section | Mother's unwillingness to cooperate, midwifery problems, use of Entonox and spinal and epidural anesthesia, chewing gum less than 20 min, watching virtual reality film less than 20 min | Migraine, headache, dizziness, motion sickness, epilepsy, psychiatric disorders, visual or auditory disabilities, history of cesarean section | Migraine, headache, dizziness, motion sickness, epilepsy, psychiatric disorders, visual or auditory disabilities, history of cesarean section | Use of pharmacologic analgesia, age < 18, hearing or vision deficits, psychiatric disorders, seizure history, predisposition for motion sickness, requiring an interpreter | Current use of pharmacologic analgesia, age < 18 or > 45, fetal or placental anomaly, high-risk pregnancy, fetal concerns requiring urgent delivery, inability to indicate pain intensity, requiring interpreter, hearing or vision deficits, psychiatric disorders, seizure history, predisposition for motion sickness |
Health status | Healthy, low-risk pregnancy | Low risk of pregnancy without obstetric complication | Low risk of pregnancy without obstetric complication | Healthy, term pregnancy | Healthy, no risks regarding the pregnant woman and foetus | Healthy, low risk pregnancy | Healthy, no chronic medical conditions or pregnancy complications | Healthy, no chronic medical conditions or pregnancy complications | Healthy, no chronic medical conditions or pregnancy complications | Healthy, low-risk pregnancy |
Intervention Details | | | | | | | | | | |
Description of the VR intervention | Simulated environment with nature scenes and sounds, presented in 360 degrees video, each intervention lasted 10 minutes during contractions | VR distraction sequence scenery like river, beach, waterfall, lake, developed by Festivo©, presented using smartphone Lenovo K4 Note VR series. Each intervention lasted 10 minutes during labor. | Video of newborn photographs with classical music (Beethoven-Moonlight Sonata), video of newborn photograph album, introductory film of Turkey, classical music (Beethoven-Moonlight Sonata), routine hospital care | Labor protocol visualization by applied VR containing imagery of blossoming tree, ocean waves, crackling campfire with meditative auditory guidance specific to pregnancy and laboring women | Ultrasound images of the foetus recorded on the 28th week of pregnancy shown with VR glass during labor process | Virtual reality glasses containing 360-degree video with nature landscapes (Samsung Gear VR Virtual Reality Headset with Samsung Mobile S7), performed twice (4–5 cm and 7–8 cm dilatations), each intervention lasted 20 min | Samsung Gear VR Headset streaming a game with pleasant sounds (flow of water), simulating a sea shore, used from early labor (4 cm dilation) for at least 20 minutes until the end of the first stage of labor | Oculus Quest All-in-one VR Gaming Headset with Nature Treks environments, used in early labor (3 cm dilation) for 20 min and after epidural analgesia in active labor (6–7 cm dilation) for 20 min | Oculus Go headset with Ocean Rift scuba diving simulation, playful dolphins scene with accompanying dolphin sounds, breathing sounds, and classical music | Ocean Rift scuba diving simulation with manatee calls and underwater breathing sounds, additional relaxing music from Brain.fm |
Type of VR equipment used | Head-mounted display powered by Samsung S3, noise reduction headphones | Smartphone Lenovo K4 Note VR series | Samsung Gear VR2 VRG | VR goggle set | VR Box 3D virtual reality glass | Samsung Gear VR Virtual Reality Headset with Samsung Mobile S7 | Samsung Gear VR Headset | Oculus Quest All-in-one VR Gaming Headset | Oculus Go headset | Samsung GearVR head-mounted display, Galaxy S7 phone, noise-reducing headphones powered by parallel S5 phone |
Stage(s) of labor during which VR was used | First and second stages | Latent phase (1–3 cm dilatation), Active phase (4–5 cm, 7–8 cm dilatation) | Active phase (5–7 cm dilatation) | During labor with pain scores of 4 to 7 | During labor | Active phase (4–5 cm and 7–8 cm dilatations) | Early labor (4 cm dilation) until the end of the first stage of labor | Early labor (3 cm dilation) and active labor (6–7 cm dilation) | Active labor | First stage of labor during unmedicated contractions |
Control group details | Usual care | Usual care | Routine hospital care | No additional intervention (usual care) | Routine procedures in the hospital | Routine maternity unit care according to national protocol | Standard care without VR intervention | Standard care without VR intervention | No VR intervention, standard care | Unmedicated labor without analgesics, alternative therapies, or systematic distraction |