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Not yet recruitingNCT07660471MBCPUpdated Jun 22, 2026

Mindfulness-Based Intervention in Primiparous Pregnant Women

An interventional study of Mindfulness-Based Intervention in Pregnancy, Fear of Childbirth and Childbirth Self-efficacy, sponsored by Agri Ibrahim Cecen University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by Agri Ibrahim Cecen University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
128
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Pregnancy
  • Fear of Childbirth
  • Childbirth Self-efficacy
  • Self-Compassion

Keywords

  • Mindfulness
  • Mindfulness-Based Intervention
  • Pregnancy
  • Primiparous Pregnant Women
  • Fear of Childbirth
  • Childbirth Self-Efficacy
  • Self-Compassion
  • Maternal Mental Health
  • Randomized Controlled Trial
03

In context

Lead sponsor

Agri Ibrahim Cecen University is the lead sponsor of 40 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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
  • Willingness to participate in the mindfulness-based intervention program

Exclusion criteria

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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
128 participants (estimated)

Study arms

  • Experimental
    Mindfulness-Based Intervention Group

    Participants in this group will receive a four-week mindfulness-based intervention consisting of eight sessions focused on breathing awareness, body awareness, emotional awareness, self-compassion, and mindfulness-based coping strategies for childbirth preparation.

    Behavioral: Mindfulness-Based Intervention

  • No intervention
    Routine Antenatal Care Group

    Participants will receive routine antenatal education and standard prenatal care. No mindfulness-based intervention will be administered.

Interventions

  • BehavioralMindfulness-Based Intervention

    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.

06

What researchers measure

Primary outcomes

  1. Childbirth Self-Efficacy

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

    Time frame: Baseline and 4 weeks after intervention

  2. Fear of Childbirth

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

    Time frame: Baseline and 4 weeks after intervention

  3. Self-Compassion

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

    Time frame: Baseline and 4 weeks after intervention

07

Study locations

1 site
  • Healthy Life Center Pregnancy School
    Ağrı, Turkey (Türkiye)
08

References and documents

Publications

  • Feli R, Heydarpour S, Yazdanbakhsh K, Heydarpour F. The effect of mindfulness-based counselling on the anxiety levels and childbirth satisfaction among primiparous pregnant women: a randomized controlled trial. BMC Psychiatry. 2024 Dec 31;24(1):964. doi: 10.1186/s12888-024-06442-3. PubMed 39741245 ↗

Related links

Individual participant data

Plan to share: No — Individual participant data will not be publicly available in order to protect participant confidentiality and privacy. Only de-identified aggregate study results will be reported.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07660471
Lead sponsor
Agri Ibrahim Cecen University
Responsible party
Ebru SOLMAZ (Lecturer Doctor, Agri Ibrahim Cecen University) — Principal investigator
First posted
Jun 22, 2026
Start date
Jun 1, 2026 (estimated)
Primary completion
Oct 31, 2026 (estimated)
Completion
Oct 31, 2026 (estimated)
Last update
Jun 22, 2026

Study contacts

Ebru Solmaz, PhD
Contact
esolmaz@agri.edu.tr
+905377737260

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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