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Research on the Construction of Cord Blood Storage Decision Aid Network Platform Based on "Internet +"

Q

Qianfoshan Hospital

Status

Enrolling

Conditions

Pregnant Women

Study type

Observational

Funder types

Other

Identifiers

NCT06001905
YXLL-KY-2023(059)

Details and patient eligibility

About

Cord blood, as an important alternative source of hematopoietic stem cells, can be used to reconstruct bone marrow hematopoietic and immune function, and is an effective means to treat children with blood diseases. However, at present, the collection rate of cord blood is not high in our country, only the mother have the right to decide whether or not. At the same time, domestic studies on cord blood collection are still very limited, for the lack of effective programs and policies, which can not provide help to improve the collection level of cord blood. Therefore, in order to improve the rate of umbilical cord blood collection, it is particularly necessary to build tools to help pregnant women decide whether to retain cord blood. This topic will investigate and analyze the cognition and retention intention of pregnant women for umbilical cord blood collection. At the same time, the related process of pregnant women for umbilical cord blood retention will be deeply explored. Based on the results of quantitative and qualitative investigation, Internet technology will be used to build a network platform for pregnant women for umbilical cord blood storage decision AIDS, and the effectiveness of this tool will be evaluated. To provide theoretical basis for clinical medical workers and umbilical cord blood bank staff to establish the decision plan of cord blood storage.

Enrollment

400 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Li Chang'e, master; Ji Hong, master

Data sourced from clinicaltrials.gov

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