Actively Recruiting

Phase Not Applicable
Age: 2Years - 25Years
All Genders
NCT05058508

LCI-PED-NOS-EXER-001: Exercise in Pediatric Oncology Patients

Led by Wake Forest University Health Sciences · Updated on 2026-01-22

60

Participants Needed

1

Research Sites

190 weeks

Total Duration

On this page

Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

A

Atrium Health Levine Cancer Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to see if there are physical and emotional benefits to participating in a structured exercise regimen for those who are ages 2-25, are newly diagnosed with a blood or solid tumor cancer, and are currently undergoing or will begin cancer treatment.

CONDITIONS

Official Title

LCI-PED-NOS-EXER-001: Exercise in Pediatric Oncology Patients

Who Can Participate

Age: 2Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 2 to 25 years at time of consent
  • Newly diagnosed cancer and planning to undergo at least 3 full cycles of chemotherapy or systemic cancer treatment
  • Ability to read and understand English or Spanish
  • Ability to understand and follow study procedures for the entire study
  • Enrollment allowed up to 21 days after starting cancer treatment
  • Receiving care at Levine Children's Cancer and Blood Disorders Clinic
  • Not participating in another clinical trial that prevents joining this study
Not Eligible

You will not qualify if you...

  • Known heart problems that make exercise unsafe
  • Uncontrolled illness, psychiatric condition, or social situation limiting study compliance or safety
  • Recent or planned surgery within 4 weeks that limits mobility, unless exercise can be modified
  • Primary central nervous system tumor
  • Osteosarcoma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Levine Children's Hospital

Charlotte, North Carolina, United States, 28203

Actively Recruiting

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Research Team

M

Meg Lattanze

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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