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Virtual Reality-Based and Face-to-Face Relaxation Programs in Pregnant Women With Preeclampsia

StatusRecruiting
PhaseNot applicable
Started2025-09-08
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 10, 2026 (before its estimated September 1, 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2026-06-07
minor
Study Status, Arms and Interventions v3
Re-verified, no change to tracked fields
2025-09-19
notable
Not Yet Recruiting→Recruiting Study Status, Outcome Measures, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-09-01→confirmed 2025-09-08
Study sites0→1
2025-08-15
minor
Study Identification, Study Status, Oversight, Outcome Measures v1
Primary completion date2026-07-01→2026-09-01
Completion date2026-12-01→2026-09-01
Start date2025-07-01→2025-09-01
Primary endpoints8 entries, revised
SalivaryHeart CortisolRate TestVariability (HRV) Measurement via Photoplethysmography (PPG)
Study titlerevised
Virtual Reality-Based and Face-to-Face Relaxation Programs in Pregnant Women withWith Preeclampsia
2025-03-18
minor
Original filing
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 fetal health, increasing the likelihood of organ damage, preterm birth, and long-term cardiovascular and neurodevelopmental complications. Non-pharmacological interventions, including relaxation techniques, have been explored for symptom management. Progressive muscle relaxation (PMR) has shown efficacy in reducing stress, anxiety, and blood pressure. Recently, virtual reality (VR)-based relaxation techniques have gained attention for enhancing stress relief and improving health outcomes. This study aims to compare the effects of VR-based PMR with in-person PMR on maternal and fetal outcomes in preeclamptic pregnancies.
Trial Details
NCT Number NCT06893510
Lead Sponsor Istanbul University - Cerrahpasa
Conditions Pre-Eclampsia, Maternal Health, Relaxation, Virtual Reality, Fetal Monitoring
Enrollment 96 participants
Start Date 2025-09-08
Primary Completion 2026-09-01 (estimated)
Study Completion 2026-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-10