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Examining a Training Program for for Acute Lymphoblastic Leukemia Childhood Cancer Survivors (JUMP)

University of Maryland Baltimore (UMB) logo

University of Maryland Baltimore (UMB)

Status

Completed

Conditions

Childhood Cancer

Treatments

Behavioral: JUMP

Study type

Interventional

Funder types

Other

Identifiers

NCT05086354
HP-00078339

Details and patient eligibility

About

Acute lymphoblastic leukemia (ALL) is the most common pediatric malignancy, with the peak incidences occurring in children two to five years of age. Children with ALL received neurotoxic chemotherapy agents for two to three years that causes decreased distal muscle strength and poor timing of muscle activation. After completion of medical treatment, ALL childhood cancer survivors (ALL CCS) are more likely to have an inactive lifestyle, resulting in life-long gross motor proficiency differences compared to their peers. ALL CCS typically do not utilize physical therapists' expertise after medical treatment has been completed. There are limited physical therapy (PT) intervention studies for ALL CCS.

Full description

We are performing a feasibility study to examine a movement based intervention that utilizes fast movements through jumping rope to improve balance, coordination, movement speed, and movement agility. The abilities to generate fast movements are required to perform functional activities and for playing sports. Participants will receive five in-person PT sessions and a home program for six weeks. The goal of this research is to determine the feasibility, acceptability, and promise of a PT program that emphasizes fast movements in ALL CCS.

Enrollment

10 patients

Sex

All

Ages

6 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children 6-17 years old
  • Completed medical treatment for ALL within the past five years (1 to 60 months)
  • Speak English.

Exclusion criteria

  • Diagnosis of a neurological disorder such as cerebral palsy, Down syndrome
  • Currently receiving PT services.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

One group that all receive the intervention of jumping rope.
Experimental group
Description:
All participants will be in one group. Every participant receives the same intervention.
Treatment:
Behavioral: JUMP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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