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Clinical Trials in Turkey / NCT07660393
Recruiting Not applicable

The Use of Virtual Reality Glasses in Women With Premature Rupture of Membranes

NCT07660393 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-16
Last updated
2026-08-11

Condition(s) studied

Fetal Health AnxietyPrenatal DistressPrenatal Attachment

Investigational drug(s) / intervention(s)

Standard prenatal careNature-themed video

Standard prenatal care: The control group will receive standard prenatal care and treatment provided by the hospital. After the study is completed, control group participants will be shown nature-themed videos via Virtual Reality Glasses (VRG) if they wish.

Nature-themed video: Pregnant women with premise rupture of membranes (PRM) in the intervention group will be shown a nature-themed video prepared by the researchers with nature sounds via Virtual Reality Glasses (VRG) twice a day for at least five minutes each time for three days.

Study summary

The Effect of Virtual Reality Glass Use on Fetal Health Anxiety, Prenatal Distress, and Maternal-Fetal Attachment in Women with Premature Rupture of Membranes: A Randomized Controlled Trial

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being 18 years of age or older * Being nulliparous * Having a diagnosis of preterm premature rupture of membranes (PPROM) * Being between 24 and 37 weeks of gestation * Having a singleton pregnancy * Being hospitalized in the ward for at least 3 days * Having no visual or hearing impairment * Being communicative and mentally and psychologically healthy * Being able to speak and express oneself in Turkish Exclusion Criteria: * Having an additional diagnosis besides preterm premature rupture of membranes (PPROM) (e.g., preeclampsia, fetal distress, fetal anomalies, gestational diabetes, bleeding, etc.) * Having a chronic disease (e.g., hypertension, diabetes mellitus, thyroid disorders, etc.) * Having conceived through assisted reproductive technologies (ART) * Having any skin infection.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Seyhan Çankaya Konya Turkey (Türkiye) Recruiting

More Selcuk University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07660393 on ClinicalTrials.gov ↗ ← All trials in Turkey