Building a decision aid platform for cord blood storage for 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 study aims to improve the collection rate of cord blood by creating a decision aid network platform for pregnant women. It will investigate the awareness and intentions of pregnant women regarding cord blood collection, focusing on their decision-making processes. The study will analyze factors influencing their choices and explore the necessary tools to assist them in making informed decisions about cord blood retention. By addressing the current limitations in cord blood collection practices, the study seeks to enhance understanding and support for pregnant women in this area.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age \> 18 years old;

  * Pregnant women whose gestational age ≥12 weeks and registered in our hospital;

    * With a certain level of education, can complete the questionnaire independently;

      * Informed consent to participate in the study

Exclusion Criteria:

* There are patients with mental illness;

  * Participated in other clinical studies in the past three months.

Where it's running

• Zhongguo
  Jinan, China Recruiting

Study contacts

• Study coordinator: Ji Hong, master
• Email: honghongji-2005@163.com
• Phone: 13791120369

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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.