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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06001905
Other study ID # YXLL-KY-2023(059)
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 10, 2022
Est. completion date July 10, 2024

Study information

Verified date August 2023
Source Qianfoshan Hospital
Contact Ji Hong, master
Phone 13791120369
Email honghongji-2005@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date July 10, 2024
Est. primary completion date July 10, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Zhongguo Jinan

Sponsors (2)

Lead Sponsor Collaborator
Qianfoshan Hospital Shandong Nursing Association

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Construct the network platform of cord blood storage decision aid tool Construct the network platform of cord blood storage decision aid tool based on "Internet +" and apply it to clinical practice to provide support and help for pregnant women in cord blood storage decision, avoid decision regret, and improve pregnant women's willingness and satisfaction in cord blood storage. 2024.07.10
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