Feasibility and Acceptability of Remote Saliva Collection

StatusRecruiting
PhaseNot specified
Started

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Record History

  1. Study First Submitted
The purpose of this study is to evaluate the practicality and acceptability of collecting biological samples and health information from childhood survivors of acute lymphoblastic leukemia (ALL) and their siblings. Participants will provide saliva, blood, hair, and fingernail samples, complete questionnaires, and participate in sleep monitoring. The information collected will help researchers understand how cancer treatment and neighborhood conditions may affect stress hormones, inflammation, and long-term health. Primary Objective \- To evaluate the feasibility of collecting multiple biological specimens, surveys, and sleep assessment among child and adolescent survivors of ALL and their siblings.
Trial Details
NCT Number NCT07884474
Lead Sponsor St. Jude Children's Research Hospital
Collaborators: National Cancer Institute (NCI)
Conditions
(from sponsor)
Survivors of Childhood Cancer, Acute Lymphoblastic Leukemia, Childhood
Related terms Precursor Cell Lymphoblastic Leukemia-Lymphoma
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov