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Clinical Trial Summary

The goal of this research study is to learn whether investigators can successfully give the PediRISE program to families-in other words, whether most families are interested in participating in a study about the PediRISE program, including a 50-50 chance of receiving standard usual care, and a 50-50 chance of receiving the PediRISE support program. The names of the study groups in this research study are: - PediRISE Program Group - Usual Care Group


Clinical Trial Description

This is a pilot, multi-center, randomized research study for the feasibility of the administration of the PediRISE program among 40 poverty exposed children with newly diagnosed cancer. Randomization means there is an equal chance of being assigned to the PediRISE Program Group or the Usual Care Group. Study procedures include screening for eligibility, study visits, and completion of surveys and questionnaires. Participation in this study will last for about 6-months. It is expected that about 40 pediatric participants with parents/guardians will take part in this research study. This study is being supported by grants from the American Cancer Society and the Children's Cancer Research Fund. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06283251
Study type Interventional
Source Dana-Farber Cancer Institute
Contact Kira Bona, MD, MPH
Phone 617-632-4688
Email Kira_Bona@dfci.harvard.edu
Status Not yet recruiting
Phase N/A
Start date June 2024
Completion date December 31, 2024

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