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Effect of Video -Based vs Standard ınformation on Maternal Anxiety and Procedure Decision in Pregnant Woman Offered Amniocentesis or Cvs

RecruitingNAAges 18 Years - 45 YearsFemaleAnkara City Hospital Bilkent
NCT07876726 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This prospective study evaluates the impact of video-based patient education compared to standard verbal informed consent on state anxiety levels and procedure acceptance rates in pregnant women undergoing invasive prenatal diagnostic testing (amniocentesis or chorionic villus sampling). Participants are assigned to four groups based on their video preference and procedural recommendation to assess changes in anxiety scores (STAI-S) before and after counseling, as well as final decisions regarding the procedure.

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📋 Eligibility rules (as published)
Inclusion Criteria * Presenting to the Perinatology Unit, * Aged between 18 and 45 years, * Having a singleton and live pregnancy, * Recommended for invasive prenatal diagnostic testing due to medical indications, * Proficient in reading, writing, and understanding the Turkish language, * Willing to participate in the study (consenting to informed consent). Exclusion Criteria: * Having a history of psychiatric disorders or depression, * Currently using psychiatric/psychotropic medication, * Having a history of invasive procedures in previous pregnancies, * Having a multiple pregnancy, * Having visual, auditory, or cognitive impairments, * Leaving more than 3 questions unanswered in the data collection tools (scales and forms) or withdrawing/dropping out of the study before completion.
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What it tests

  • Multilingual Video-Based Patient Education
  • Standard Verbal Informed Consent
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Where

1 site
Ankara Bilkent City Hospital
Ankara, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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