Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Exercise study of fitness and lungs in young people with childhood illness

Studies fitness and lung function in young people after leukemia, heart transplant, or lung disease.

Plain-language title generated from the registry record
Registry title: Fitness and Lung Function Among Survivors of Heart Transplant, Leukemia and Infant BPD Through Exercise

Key facts

Where
Minneapolis, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 8 and 25 years old?

Source: NCT05025774, who can take part

Where in United States

  • Masonic Cancer CenterMinneapolis, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Masonic Cancer Center, University of Minnesota
Trial code
NCT05025774
Record updated
24 November 2025
Original description
This study aims to more accurately assess cardiac function, ventilation and exercise capacity in a non-invasive fashion, and to better characterize exercise intolerance in the setting of three populations of individuals with chronic diseases of childhood (acute lymphoblastic leukemia (ALL), chronic lung disease (CLD) of prematurity, and post-heart transplant (HT))Read full original descriptionShow less

Fitness and Lung Function Among Survivors of Heart Transplant, Leukemia and Infant Bronchopulmonary Dysplasia (BPD, Also Known as Chronic Lung Disease of Prematurity) Through Exercise (FLASHLITE)

This study aims to more accurately assess cardiac function, ventilation and exercise capacity in a non-invasive fashion, and to better characterize exercise intolerance in the setting of three populations of individuals with chronic diseases of childhood (acute lymphoblastic leukemia (ALL), chronic lung disease (CLD) of prematurity, and post-heart transplant (HT))

Inclusion: Cases:; Acute lymphoblastic leukemia survivor, OR living with chronic lung disease of prematurity, OR living with heart transplant; 8-25 years old; Height: ≥ 48 inches; Ambulatory without assistance; English speaking; Normotensive (<95th percentile for age; okay if managed with antihypertensive medication); SpO2 >92%; Not pregnant; ALL survivor specific: must have completed therapy ≥ 3 months prior to study entry; Controls; 8-25 years old; Height: ≥ 48 inches; Ambulatory without assistance; English speaking; No history of arrhythmia or known cardiac dysfunction at baseline; Normotensive (<95th percentile for age; okay if managed with antihypertensive medication); SpO2 >95%; Not pregnant.

Exclusion: Cases:; ALL specific: received cranial radiation, bone marrow transplant recipients; Investigator or patient's primary physician deems the patient unsuitable for the study; Controls:; History of malignancy, CLD or HT or any other diagnosis which may reduce cardiorespiratory function; Investigator deems the patient unsuitable for the study.

ClinicalTrials.gov NCT05025774