Virtual Reality-Based and Face-to-Face Relaxation Programs in Pregnant Women With Preeclampsia
Recruiting
N/A
Interventional Study
Pre-Eclampsia
Maternal Health
Relaxation
Virtual Reality
Fetal Monitoring
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 96 (estimated)
- Sponsor
- Istanbul University - Cerrahpasa · Other
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About This Trial
Preeclampsia, affecting 2-8% of pregnancies globally, is a leading hypertensive disorder in pregnancy. It is clinically characterized by elevated blood pressure (≥140/90 mmHg) after the 20th gestational week, often accompanied by proteinuria and systemic complications such as thrombocytopenia, liver dysfunction, and cerebral symptoms. This condition poses significant risks for both maternal and fe…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Hospitalized with a diagnosis of preeclampsia.
* Gestational age ≥26 weeks.
* 18 years or older.
* Singleton and viable pregnancy.
* Willing to participate in the study voluntarily.
Exclusion Criteria:
* Multiple pregnancy.
* Pregnancy achieved through assisted reproductive …
Contacts