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Study identifier: NCT05154305 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Multidisciplinary Rehabilitation of Children and Adolescents After Acute Cancer Treatment

Condition: Cancer Survivors · Rehabilitation · Exercise Therapy  ·  Sponsor: University Hospital, Ghent

PhaseNA
Planned participants60
Who can joinAll sexes, 8 Years to 21 Years
Healthy volunteersNo

About this study

Recent numbers display a 85% survival-rate in children after a very harmful disease such as cancer. However, the survivors still experience mild to severe side effects of the primary disease or treatment. A long time follow-up in the University Hospital of Ghent in children with cancer displays important long term side effects such as: reduced muscle strength; reduced endurance capacity; reduced exercise tolerance; fatigue; disturbed body composition with increased risk for obesity and/or diabetes and osteoporosis; and neuropathic damage and myopathy. These physical complaints have a significant impact on the activities and participation in daily living. The purpose of this interventional study is to create a rehabilitation program for children after acute cancer treatment. The goal is to minimalize the previous described long term side effects of the disease. The current study should allow us to determine the effects of the intervention at the level of functioning, activities and participation. In addition, we account for the environment and personal factors as described by the International Classification of Functioning, disability and health (ICF-criteria). The study population consists of children between 8 and 11 years and adolescents of 12 to 21 years old. All participants receive a multidisciplinary treatment for 4 months, guided by a team which includes: oncologist, rehabilitation doctor, physical therapist, dietitian, psychologist, and occupational therapist. At …

This description comes directly from the study's public registry record.

Talk to the study team

Catharina Dhooge, MD, PhD  ·  00329/3322452  ·  CATHARINA.DHOOGE@UZGENT.BE

Ruth Van Der Looven, MD  ·  00329/332.69.39  ·  RUTH.VANDERLOOVEN@UZGENT.BE

Always discuss trial participation with your own doctor first.

Locations (1)

Ghent University HospitalGhent, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT05154305