The Use of Virtual Reality Glasses in Women With Premature Rupture of Membranes
Recruiting · NCT07660393 · Interventional (participants receive a specific treatment) · Lead sponsor: Selcuk University
View the official record on ClinicalTrials.gov →Interventions studied
Nature-themed videoStandard prenatal care
What this trial is about
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
Who can take part
Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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.
Where it is running
1 location listed.
- Seyhan Çankaya - Konya, Turkey (Türkiye)