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NCT Number: NCT04815447

Cardiopulmonary Fitness and Its Clinical Determinants of a Population of Childhood Cancer Survivor

Medical progress have made it possible to considerably improve the survival of children with an oncological disease. Currently, the survival rate increased to above 90 % in the most developed countries . This increase of childhood cancer survivors (CCS) asks us about their future and their quality of life. Assessing health related life quality , previous studies observe that in this particular population of patients, it is related to a poor physical capacity , physical activity level and many of these patients do not meet the activity level recommended by the world health organization due to fatigability and sedentary behaviours . In addition to these habits, the CCS are more susceptible to develop cardiovascular risk (CVR) leading to cardiovascular disease in adulthood and increases them mortality . Furthermore, CCS who have been experiencing hematopoietic stem cells transplantation (HSCT) are more susceptible to develop these CVR. In parallel with the common CVR, lower cardiopulmonary fitness assessed by cardiopulmonary exercise test (CPET) in the general population has been established as a major and independent CVR for cardiologic events.

Cardiopulmonary fitness assessed by maximal cardiopulmonary exercise test (CPET) allows physicians to measure metabolic response to maximal effort in a population that is known as VO2max. This domain of applied physiology permits a new way to approach the understanding of global health prognosis in chronic disease. For example, decrease of VO2max is involved in lower quality of life in patients with congenital heart disease. Cardiopulmonary exercise test for VO2max exploration has been demonstrated feasible in child patients with leukemia or other tumors after intensive chemotherapy, prior to HSCT.

Assessment of cardiopulmonary fitness in CCS is already described in previous studies, but this study aimed to compare a maximal CPET assessment on a large childhood cancer survivors cohort with healthy control, on a quite young cohort, during the oncologic follow up and find out its determinants.

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Key information

Age range

6 year–25 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Uh Montpellier

Montpellier, 34295, France

About this study

This is a controlled, monocentric, cross-sectional study conducted in a tertiary care center for oncologic disease in children (Montpellier University Hospital, France) was carried out between November 2010 and November 2020.

Two groups were identified: CCS group and control group.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for CCS group :

  • aged between 5 and 25 years old,
  • having been complete a full regimen for oncological disease and considered in remission at the end of treatment. Remission was considered in absence of relapse or new treatment initiated before the CPET end point.

Inclusion criteria

for control group :

  • children referred for a nonsevere functional symptom linked to exercise (murmur, palpitation or dyspnoea) or for a medical sports certificate.
  • completely normal check-up, including physical examination, ECG, echocardiography and spirometry.

Exclusion criteria

for control group:

  • Children with any chronic disease, medical condition (cardiac, neurological, respiratory, muscular or renal)
  • Children with any medical treatment
  • Children requiring any further specialised medical consultation

Treatment and study plan

Primary outcomes

  1. comparison of VO2max for CCS patients compared to control children

    Time frame: 1 day

    comparison of the mean of VO2max value in ml/kg/min between CCS group and control group

Secondary outcomes

  1. comparison of ventilatory anaerobic threshold (VAT) for CCS patients compared to control children

    Time frame: 1 day

    comparison of the mean of VAT value in ml/kg/min between CCS group and control group

  2. correlation between clinical determinants and VO2max in the CCS group

    Time frame: 1 day

    with multivariate analysis, we will look for the correlation between the clinical determinants and the decreased of VO2max in CCS group.

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Collaborators

  • Pediatric Oncology Department, Montpellier University Hospital, France
  • Pediatric and Congenital Cardiology Department, Montpellier University Hospital, France

Registry information

Official study title

Cardiopulmonary Fitness and Its Clinical Determinants of a Population of Childhood Cancer Survivor: a Controlled Retrospective Study

Acronym: ONCO-SPORT

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Mar 25, 2021
Registry last updated
Apr 20, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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