HEM-SURVIVE: Structuralized Follow-up for Childhood Hematological Malignancy Survivors

Sponsor
The Children's Hospital of Zhejiang University School of Medicine
Study ID
NCT07483749
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

Eligibility Criteria

Sex
ALL
Age
1 Year - 21 Years
Healthy Volunteers
Not accepted

Study Details

This study aims to construct a structuralized follow-up model for survivors of childhood hematological malignancies in China. Using a multicenter prospective cohort design, it will identify the burden and risk factors of late effects. The study hypothesizes that a standardized follow-up path managed by an electronic platform will improve follow-up compliance and reduce the missed diagnosis rate of late effects.

Key Dates

First listed
Mar 19, 2026
Start date
Mar 25, 2026
Status verified
Dec 2025
Primary completion
Dec 31, 2028
Completion
Dec 31, 2028

Study Design

Enrollment
400 participants (estimated)

Arms

  • Arm: HEM-SURVIVE Structured Follow-up Mode
    Implementation of a structured follow-up system based on exposure-oriented risk stratification (four levels: Minimal, Standard, High, and Ultra-high risk). It includes standardized examination packages (A, A+, B, and C), multidisciplinary (MDT) survivor clinics, and digital management via the HEM-SURVIVE APP.
  • Arm: Conventional Follow-up Mode
    Routine follow-up practices currently used in China. Examination projects are determined empirically by the attending physician and family, which lacks a unified path and systematic proactive monitoring. Key examinations for late effects are often triggered only after symptoms appear.

Primary Outcome Measure

Incidence of severe late-effect composite endpoint. [ Time Frame: From the date of enrollment to the end of follow-up (up to 36 months). ]

Central Contacts

Find similar trials

Related Studies