Skip to content

Multidisciplinary Rehabilitation of Children and Adolescents After Acute Cancer Treatment

Multidisciplinary Rehabilitation of Children and Adolescents After Acute Cancer Treatment

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05154305
Enrollment
60
Registered
2021-12-13
Start date
2019-04-02
Completion date
2026-12-31
Last updated
2023-12-12

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

Conditions

Cancer Survivors, Exercise Therapy, Rehabilitation

Keywords

Multidisciplinary Rehabilitation, Cohort study, Childhood and adolescence

Brief summary

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 the beginning of the multidisciplinary program, the participants receive psychoeducation, diet advice, tips for participation, fatigue, and psychological well-being. In general, the rehabilitation program focusses on reintegration at school and leisure activity. After the first assessment, an individually adjusted physical program consisting of strength and endurance training will be made. This physical program will be executed 3 times a week, 2 times guided by a physical therapist at the University Hospital or at a private practice, and ones a week by themselves at home recorded by an activity tracker. Follow-up is foreseen on monthly basis. Participants will undergo assessment 3 times: 1) baseline (T0); 2) after 4 months treatment (T1); 3) after 1 year follow-up (T2). The purpose of this program is to encourage patients at risk for increasing their healthy habits, exercise and participation in order to decrease long-term (side) effects.

Interventions

* individually adjusted physical program consisting of strength and endurance training \> 3 times a week, 2 times guided by a physical therapist at the University Hospital or at a private practice, and ones a week by themselves at home recorded by an activity tracker. Follow-up is foreseen on monthly basis. * multidisciplinary coaching (discipline depending on personal needs of patient) on a monthly basis. These coaching sessions could be in small groups or individual.

Sponsors

VZW kinderkankerfonds, Belgium
CollaboratorUNKNOWN
University Hospital, Ghent
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 21 Years
Healthy volunteers
No

Inclusion criteria

* between 6 months and 8 years post acute cancer treatment * off medical treatment * all possible cancer diagnosis, except for brain tumors and sarcomas

Exclusion criteria

* not able to participate for 3 consecutive weeks * not able to perform a maximal cardiopulmonary exercise test * unwilling to cooperate * relapse

Design outcomes

Primary

MeasureTime frameDescription
Maximal exercise test20 minutesMaximal exercise test on a cycle ergometer
Body composition5 minutesBody composition by dietitian
Pediatric Quality of Life Inventory10 minutesassessment Quality of Life
Children's Assessment of Participation and Enjoyment (CAPE)10 minutesassessment participation
Preferences for Activities of Children (PAC)10 minutesassessment preferred activities

Countries

Belgium

Contacts

Primary ContactCatharina Dhooge, MD, PhD
CATHARINA.DHOOGE@UZGENT.BE00329/3322452
Backup ContactRuth Van Der Looven, MD
RUTH.VANDERLOOVEN@UZGENT.BE00329/332.69.39

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026