This study, called the UNC Childhood, Adolescent, and Young Adult Cancer Cohort (UNC-CAYACC), is creating a registry of children, adolescents, and young adults (up to age 39) who have been diagnosed with cancer. The goal is to gather information to help researchers better understand cancer outcomes in these age groups, especially for those aged 15-39. You can join if you are between 1 and 39 years old, speak English or Spanish, and have been diagnosed with cancer. The study will involve physical and mental assessments, questionnaires about your health and quality of life, body measurements, and providing samples for future research. The main goals are to build this registry and complete functional assessments over five years.

Study design

This is an observational study, meaning researchers will collect information without giving any specific treatments. It plans to enroll about 500 participants.

What's involved

You would complete physical and cognitive assessments, fill out questionnaires, have body measurements taken, and provide biospecimens (like blood or tissue samples).

Compensation

Not stated in the trial record.

Follow-up

The study aims to develop the registry and complete functional assessments over five years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.