Mindfulness-Based Intervention in Primiparous Pregnant Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorAgri Ibrahim Cecen University

About this trial

This randomized controlled trial aims to evaluate the effect of a mindfulness-based intervention on childbirth self-efficacy, fear of childbirth, and self-compassion among primiparous pregnant women. Eligible pregnant women will be randomly assigned to either a mindfulness intervention group or a control group receiving routine antenatal education and standard prenatal care. The intervention program will consist of eight sessions delivered over four weeks. Outcomes will be assessed before and after the intervention using validated measurement tools. The findings may contribute to the development of effective psychosocial interventions to improve maternal well-being during pregnancy.

Eligibility criteria

Qualifiers

Pregnant women aged 18 years and older

Primiparous women

Singleton pregnancy

Gestational age between 28 and 32 weeks

Disqualifiers

Multiple pregnancy

High-risk obstetric complications (e.g., preeclampsia, gestational diabetes, placenta previa)

Diagnosed severe psychiatric disorders (e.g., psychotic disorders, bipolar disorder)

Substance or alcohol dependence

Trial design

Treatments tested in this trial

  • Mindfulness-Based Intervention

Treatment groups

128 Participants
are divided into 2 treatment groups

Sponsors and collaborators