acute lymphoblastic leukemia leukemia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All subjects from the VUmc, the UMCU and the UMCN that have been treated according to the Dutch Childhood Oncology Group (DCOG) ALL-9 or ALL-10 protocol and that participated in the DREAMS I study. Healthy age and sex matched controls, existing of: 1) friends of ALL survivors who participate in the DREAMS study, 2) friends of current ALL patients in the VUmc, 3) friends of survivors of childhood cancer who visit the outpatient clinic late effects of the VUmc.
Exclusion criteria
Exclusion criteria: Prolonged glucocorticoid therapy for other reasons than treatment for ALL. Chronic health conditions that might influence HPA axis activity.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HPA axis regulation (cortisol) and sympathetic nervous system activity (blood pressure, heart rate) during relaxation and during the Trier social stress test. | — |
Secondary
| Measure | Time frame |
|---|---|
| The association between HPA axis activity and sympathetic nervous system activity and fatigue and quality of life. | — |
Countries
Netherlands