Mindfulness program for first-time pregnant women

Is this trial a fit for you?

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

What this trial studies

This interventional study compares a mindfulness-based stress reduction program to standard care in nulliparous pregnant women between 12 and 28 weeks of gestation. Participants are randomly assigned to the mindfulness program or a control group. The program focuses on stress-reduction techniques, body awareness, and coping strategies to support psychological well-being during pregnancy. Outcomes include prenatal anxiety, concerns about fetal health, and overall psychological well-being. The study is conducted at Amasya University and affiliated hospital sites.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Be 18 years of age and older,
* Have at least a primary school graduate
* Not having given birth before
* Be between the 12th and 28th weeks of pregnancy,
* Have internet access

Exclusion Criteria:

* Having any communication problems (language, hearing, vision, speech, etc.),
* Having a diagnosis of high-risk pregnancy, or having a diagnosis of a psychiatric illness (depression, psychosis, etc.)

Where it's running

• Amasya University Sabuncuoğlu Şerefeddin Training and Research Hospital
  Amasya, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: ELİF KETEN EDİS, Assoc. Prof., PhD
• Email: elifketen05@gmail.com
• Phone: +903582115005

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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.