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Perinatal Anxiety / Virtual Reality Forest Mindfulness Intervention / Perinatal Depression · Interventional Study
ClinicalTrials.gov · August 18, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a study registration for a randomized controlled trial comparing virtual reality forest-based mindfulness to conventional mindfulness for perinatal anxiety and depression. No results are available in this registry record; the study is currently recruiting and has not yet reported outcomes.
Interventional, Randomized, Parallel, Open label, Prevention purpose. Perinatal Anxiety, Perinatal Depression, Maternal Mental Health; Female; age from 18 Years; accepts healthy volunteers. Intervention: VR-Based Mindfulness Intervention. Compared with: Conventional Mindfulness Intervention — Active Comparator. n = 100. 1 site: Taiwan.
This is a study registration for a randomized controlled trial comparing virtual reality forest-based mindfulness to conventional mindfulness for perinatal anxiety and depression. No results are available in this registry record; the study is currently recruiting and has not yet reported outcomes.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
Results from this trial, once available, may inform whether immersive virtual reality enhances engagement and efficacy of mindfulness-based interventions for perinatal mental health compared to conventional approaches. Until results are reported, no clinical recommendation can be made.
This is a registry record for an ongoing, actively recruiting randomized controlled trial with no results yet reported; it describes planned methods and endpoints only.
As stated by the source record.
Quoted from the source exactly as published.
Results from this trial, once available, may inform whether immersive virtual reality enhances engagement and efficacy of mindfulness-based interventions for perinatal mental health compared to conventional approaches. Until results are reported, no clinical recommendation can be made.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07606248). This is a study registration, not published results. Lead sponsor: National Taiwan University Hospital. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 100 participants (ESTIMATED). Conditions: Perinatal Anxiety, Perinatal Depression, Maternal Mental Health. Interventions: BEHAVIORAL: Virtual Reality Forest Mindfulness Intervention; BEHAVIORAL: Conventional Mindfulness Intervention. Primary outcome measures: Generalized Anxiety Disorder-7 (GAD-7) Score , Baseline (20-24 weeks gestation), post-intervention (32 weeks gestation to before delivery), and 1 month, 3 months, and 6 months postpartum; Edinburgh Postnatal Depression Scale (EPDS) Score , Baseline (20-24 weeks gestation), post-intervention (32 weeks gestation to before delivery), and 1 month, 3 months, and 6 months postpartum. Brief summary: Perinatal anxiety and depression are common mental health concerns that may negatively affect maternal well-being, infant development, and family functioning. Mindfulness-based interventions have shown beneficial effects on reducing psychological distress during pregnancy; however, maintaining attention and engagement during mindfulness practice may be challenging for some pregnant women. This randomized controlled trial aims to evaluate the feasibility and effectiveness of an integrated virtual forest environment and mindfulness-based intervention for improving mental health in perinatal women. Pregnant women between 20 and 24 weeks of gestation will be randomly assigned to either an experimental group receiving virtual reality (VR)-based forest mindfulness intervention or a control group receiving conventional mindfulness intervention. Both groups will participate in a 9-week mindfulness program and receive app-based mindfulness practice. The experimental group will additionally receive immersive VR forest-based mindfulness sessions during prenatal visits. Outcomes including anxiety, depression, mindfulness awareness, physiological indicators, and intervention acceptability will be assessed during pregnancy and postpartum follow-up.
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