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Medical assessment of adverse health outcomes in Dutch childhood cancer survivors; a nationwide project; DCOG LATER Q2008 onderzoek: Bone mineral density and body composition in survivors of childhood cancer

Medical assessment of adverse health outcomes in Dutch childhood cancer survivors; a nationwide project; DCOG LATER Q2008 onderzoek: Bone mineral density and body composition in survivors of childhood cancer - DCOG LATER Q2008 - bone

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47723
Enrollment
2500
Registered
2015-01-23
Start date
2016-05-04
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

botten, bewegingsapparaat en fitheid impaired fitness and motor impairment osteonecrosis osteoposoris

Interventions

None listed

Sponsors

Stichting Kinderoncologie Nederland
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients who were treated for childhood cancer (before age 18) in one of the Pediatric Oncology Centers between 1960 and 2001 and who survived for at least 5 years after diagnosis will be included in the DCOG LATER study. Participating centres are located in Amsterdam (VU University Medical Center (VUMC)), Groningen (Children's Cancer Center/ University Medical Center Groningen (UMCG)), Rotterdam (Rotterdam Erasmus MC-Sophia (REMC-S), Nijmegen (University Medical Center Nijmegen (UMCN)), Leiden (Leiden University Medical Center (LUMC) and Utrecht (Princess Máxima Center for Pediatric Oncology (PMC)). From this cohort, 2500 childhood cancer survivors will be asked to participate in this study. (BMI will be assessed in all 7000 survivors as regular patient care).

Exclusion criteria

Exclusion criteria: diagnosis of childhood cancer with survival less than 5 years, age at diagnosis >17 years or diagnosis while residing in foreign country, no cardiologic impairment(fitness)

Design outcomes

Primary

MeasureTime frame
1- Prevalence and exogenous and genetic risk factors of osteopenia and osteoporosis and subsequent fractures, per persons years in CCS. 2- Prevalence of over- and underweight as expressed by BMI and LBM. 3- Treatment and diagnosis related risk factors for irreversible osteonecrosis. 4- Treatment and diagnosis related risk factors for impaired motor function and muscle strength

Secondary

MeasureTime frame
N.A.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)