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NCT05025774Recruiting

Fitness and Lung Function Among Survivors of Heart Transplant, Leukemia and Infant BPD Through Exercise

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)

Source: ClinicalTrials.gov · Last updated 24 Nov 2025

Brief summary (registry, in English)

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))

Status (registry)
Recruiting
Study type
Observational
Enrollment
90 (estimated)
First submitted
5 Aug 2021
Start date
14 Mar 2025
Primary completion date
1 Nov 2026
Lead sponsor
Masonic Cancer Center, University of Minnesota
NCT number
NCT05025774

What you commit to

  • Study type: Observational
  • Planned participants: 90
  • From 14 Mar 2025 to the primary completion date, 1 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Cases:
    • ALL specific: received cranial radiation, bone marrow transplant recipients
    • Investigator or patient's primary physician deems the patient unsuitable for the study

Other illness

  • Controls:
    • History of malignancy, CLD or HT or any other diagnosis which may reduce cardiorespiratory function
    • Investigator deems the patient unsuitable for the study

Who the study is looking for

  • 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

Age in the registry: 8 years to 25 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Masonic Cancer Center
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.