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Perinatal Anxiety / Group Discussion / Routine Health Education · Interventional Study
ClinicalTrials.gov · September 11, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a registered randomized controlled trial comparing an 8-week mindfulness intervention to group discussion and health education in pregnant women with perinatal anxiety. The trial has completed recruitment of 356 participants, but results are not yet posted in this registry record and therefore no efficacy or safety conclusions can be drawn.
Interventional, Randomized, Parallel, Single masking, Treatment purpose. Perinatal Anxiety; Female; age from 18 Years. Intervention: Group Mindfulness Intervention. Compared with: Group Discussion — Active Comparator; Health Education — Active Comparator. n = 356. 1 site: China.
This is a registered randomized controlled trial comparing an 8-week mindfulness intervention to group discussion and health education in pregnant women with perinatal anxiety. The trial has completed recruitment of 356 participants, but results are not yet posted in this registry record and therefore no efficacy or safety conclusions can be drawn.
No efficacy or safety results are reported in this registry record
The source did not state who this applies to in practice.
This is a completed trial registry record with no results posted; the study design and planned outcomes are registered but efficacy and safety data are not yet reported in this source.
As stated by the source record.
Quoted from the source exactly as published.
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 (NCT07757243). This is a study registration, not published results. Lead sponsor: Shenzhen Kangning Hospital. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 356 participants (ACTUAL). Conditions: Perinatal Anxiety. Interventions: BEHAVIORAL: Group Mindfulness Intervention; BEHAVIORAL: Group Discussion; BEHAVIORAL: Routine Health Education. Primary outcome measures: Change in anxiety symptoms , Baseline and immediately after the 8-week intervention; Change in depressive symptoms , Baseline and immediately after the 8-week intervention; Change in fear of childbirth , Baseline and immediately after the 8-week intervention. Brief summary: This randomized controlled intervention study evaluated an 8-week group mindfulness intervention for pregnant women at 20 to 30 gestational weeks. Participants were randomized to mindfulness-based group intervention, group discussion, or health education. The study assessed anxiety, depressive symptoms, and fear of childbirth before and after intervention, and an exploratory subsample completed a pain dot-probe task to examine pain-related attention processing.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.