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NCT Number: NCT07660471

Mindfulness-Based Intervention in Primiparous Pregnant Women

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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Pregnancy is a period characterized by significant physical, psychological, and social changes. Fear of childbirth, low childbirth self-efficacy, and difficulties in self-compassion may negatively affect maternal well-being and childbirth experiences. Mindfulness-based interventions have been increasingly used to support psychological health during pregnancy; however, evidence regarding their effects on childbirth self-efficacy, fear of childbirth, and self-compassion remains limited.

This study is designed as a randomized controlled trial to evaluate the effectiveness of a mindfulness-based intervention among primiparous pregnant women attending a pregnancy school affiliated with a Healthy Life Center in Ağrı, Türkiye. A total of 128 eligible pregnant women will be randomly assigned to either an intervention group or a control group.

Participants in the intervention group will receive a four-week mindfulness-based intervention consisting of eight sessions focused on breathing awareness, body awareness, emotional awareness, non-judgmental acceptance, self-compassion, and mindfulness-based coping strategies for childbirth preparation. Participants in the control group will continue to receive routine antenatal education and standard prenatal care.

Data will be collected before and after the intervention using validated instruments assessing childbirth self-efficacy, fear of childbirth, and self-compassion. The results of this study may provide evidence for the integration of mindfulness-based approaches into antenatal care programs to enhance maternal psychological well-being and preparedness for childbirth.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women aged 18 years and older
  • Primiparous women
  • Singleton pregnancy
  • Gestational age between 28 and 32 weeks
  • No known obstetric complications
  • Ability to read and understand Turkish
  • Attendance at the Pregnancy School of the Healthy Life Center
  • Willingness to participate and provide written informed consent
  • Willingness to participate in the mindfulness-based intervention program

Exclusion criteria

  • 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
  • Previous participation in a structured mindfulness, meditation, or similar awareness-based program
  • Inability to attend intervention sessions regularly

Treatment and study plan

Mindfulness-based Intervention

Behavioral

A four-week mindfulness-based intervention consisting of eight sessions delivered twice weekly. The program includes breathing awareness, body awareness, emotional awareness, non-judgmental acceptance, self-compassion practices, and mindfulness-based coping strategies for childbirth preparation. Sessions will be delivered face-to-face and will last approximately 60-90 minutes each.

Primary outcomes

  1. Childbirth Self-Efficacy

    Time frame: Baseline and 4 weeks after intervention

    Assessment of childbirth self-efficacy using the Childbirth Self-Efficacy Scale.

  2. Fear of Childbirth

    Time frame: Baseline and 4 weeks after intervention

    Assessment of fear of childbirth using the Wijma Delivery Expectancy/Experience Questionnaire Version A (W-DEQ-A).

  3. Self-Compassion

    Time frame: Baseline and 4 weeks after intervention

    Assessment of self-compassion using the Self-Compassion Scale.

Study contacts

Contact information is provided by the study sponsor or research team.

Ebru Solmaz, PhD

CONTACT

[email protected]

+905377737260

Sponsors and collaborators

Lead sponsor

Agri Ibrahim Cecen University

Other

Registry information

Official study title

Effect of a Mindfulness-Based Intervention on Childbirth Self-Efficacy, Fear of Childbirth, and Self-Compassion in Primiparous Pregnant Women: A Randomized Controlled Trial

Acronym: MBCP

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 22, 2026
Registry last updated
Jun 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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