A cross-sectional survey on genetic counseling and genetic testing in hemophilia carrier care in Japan

A cross-sectional survey on genetic counseling and genetic testing in hemophilia carrier care in Japan - A cross-sectional survey on genetic counseling and genetic testing in hemophilia carrier care in Japan

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000060633

Enrollment

109

Registered

2026-02-09

Start date

2026-01-09

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemophilia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The physician representative of each block core hospital designated by the Hemophilia Care Network Committee of the Japan Society on Thrombosis and Hemostasis (17 institutions, excluding Tokyo Medical University Hospital). The physician representative of each regional core hospital designated by the Hemophilia Care Network Committee of the Japan Society on Thrombosis and Hemostasis (92 institutions).

Exclusion criteria

Exclusion criteria: Individuals who do not provide consent to participate in the questionnaire (i.e., do not agree / do not check the consent box)

Design outcomes

Primary

Measure	Time frame
Whether each institution provides (1) genetic counseling and (2) genetic testing-based hemophilia carrier diagnosis.	—

Countries

Japan

Contacts

Public ContactMasato Bingo

Tokyo Medical University Department of Laboratory Medicine

bingo@tokyo-med.ac.jp0333426111

Outcome results