Building a decision aid platform for cord blood storage for pregnant women
Research on the Construction of Cord Blood Storage Decision Aid Network Platform Based on "Internet +"
This study is trying to see if a new online tool can help pregnant women understand and decide whether to store their baby's cord blood.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | Qianfoshan Hospital Academic / other |
| Locations | 1 site (Jinan) |
| Trial ID | NCT06001905 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women over 18 years old, with a gestational age of at least 12 weeks, who can independently complete a questionnaire.
Not a fit: Patients with mental illnesses or those who have participated in other clinical studies in the past three months may not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly increase the rate of cord blood collection, providing more hematopoietic stem cells for treating blood diseases in children.
How similar studies have performed: While there is limited research on cord blood collection in this context, the approach of using decision aids for medical choices has shown promise in other health-related studies.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Jinan
- Zhongguo — Jinan, China (Recruiting)
Study contacts
- Study coordinator: Ji Hong, master
- Email: honghongji-2005@163.com
- Phone: 13791120369
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.