Clinical trial Recruiting at 1 site Interventional Ages 15 to 19

Mindfulness training to reduce childbirth fear and strengthen bonding and breastfeeding in pregnant teens

Official title: Effect of Mindfulness-Based Stress Reduction Training on Fear of Childbirth, Maternal and Paternal Bonding and Breastfeeding Success in Adolescent Pregnant Women and Their Partners

Run by Inonu University · NCT07540923 · Data updated 2026-11-12

This program will try mindfulness-based stress reduction (MBSR) with pregnant teens and their partners to see if it lowers fear of childbirth, improves parent–infant bonding, and increases breastfeeding success.

More Mindfulness trials

Quick facts

Study typeInterventional
Ages15 Years to 19 Years
SexAll
Enrollment54 (estimated)
SponsorInonu University
Academic / other
Locations1 site (Malatya, Malatya)
StatusRecruiting
StartedDecember 1, 2025
Main results expectedApril 30, 2026
Study endsMay 30, 2026
Registry record updatedApril 21, 2026
Trial IDNCT07540923 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are literate, first-time pregnant adolescents aged 15–19 in their 30–33 weeks of gestation who do not have high-risk pregnancies and whose partners agree to participate.

Probably not a fit

Patients with chronic medical conditions, active physical or psychiatric disorders in either partner, fetal anomalies, prior MBSR training, or those unable to complete the sessions are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled program gives MBSR training to primiparous pregnant adolescents (ages 15–19) and their partners during the third trimester and compares outcomes to routine care. Participants attend structured mindfulness sessions designed to reduce stress and childbirth fear while encouraging present-moment bonding and parenting skills. Primary outcomes include measures of fear of childbirth, maternal and paternal bonding, and breastfeeding success after birth. The intervention is delivered at Inonu University in Malatya and requires partners to participate actively.

Why it matters

Potential benefit: If successful, the intervention could lower childbirth fear and strengthen mother– and father–infant bonding while increasing the likelihood of successful breastfeeding in adolescent parents.

How similar studies have gone: Mindfulness-based programs have shown benefits for reducing perinatal anxiety and improving maternal bonding in adult populations, but evidence specifically in adolescent pregnancies and partner-included interventions is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Being between 15-19 years of age
2. Being in the third trimester of pregnancy (30-33 weeks of gestation)
3. Being primiparous
4. Having no history of miscarriage, abortion or similar obstetric problems during pregnancy
5. Not having a high-risk pregnancy diagnosis
6. Being literate
7. Partner accepting to actively participate in the parenting process

Exclusion Criteria:

1. Having a chronic disease
2. Having physical or psychological health problems
3. Having a psychiatric diagnosis in the participant or their partner
4. Having a detected health problem or congenital anomaly in the fetus
5. Having previously received Mindfulness-Based Stress Reduction (MBSR) training
6. Not completing the planned training program
7. Voluntarily withdrawing from the study

Where it's running

  • Inonu University Faculty of Medicine
    Malatya, Malatya, Turkey (Türkiye)
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.