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Completed
NCT07757243
Mindfulness for Perinatal Distress
Conditions: Perinatal Anxiety
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 356
Sponsor: Shenzhen Kangning Hospital
Location: Shenzhen Kangning Hospital Shenzhen Guangdong
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.
Eligibility Criteria
Inclusion Criteria:
* Pregnant women at 20 to 30 gestational weeks.
* No obvious pregnancy complications.
* Able to complete questionnaires independently.
* Willing to participate in the study and able to complete the 8-week intervention.
* Provided written informed consent.
Exclusion Criteria:
* Self-harm behavior or suicidal tendency.
* Current psychiatric medication use.
* Severe mental disorder, such as schizophrenia, bipolar disorder, or organic mental disorder.
* Severe somatic disease, such as abnormal liver or renal function, brain injury, heart disease, or epilepsy.
* Pregnancy complications or expected inability to complete the intervention or follow-up.
Source: ClinicalTrials.gov (NCT07757243). StuddyBuddy aggregates publicly available trial information.