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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02216604
Date of registration: 13/08/2014
Prospective Registration: No
Primary sponsor: German Cancer Research Center
Public title: Exercise in Pediatric Cancer Patient Undergoing Anti-Cancer Treatment ONKOKIDS-HD
Scientific title: Physical Activity Intervention Program for Childhood Cancer Patients Under Chemo- and/or Radiation Therapy
Date of first enrolment: May 2011
Target sample size: 50
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02216604
Study type:  Interventional
Study design:  Allocation: Non-Randomized. Intervention model: Factorial Assignment. Primary purpose: Supportive Care. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
Germany
Contacts
Name:     Joachim Wiskemann, PhD
Address: 
Telephone:
Email:
Affiliation:  National Center for Tumor Diseases
Key inclusion & exclusion criteria

Inclusion Criteria:

- pediatric cancer diagnosis (primary leukemia, brain tumors and bone tumors

- date of diagnosis not longer than 8 weeks ago

Exclusion Criteria:

- severe cardiac impairment

- bone metastasis inducing skeletal fragility

- other orthopedic diseases or any other circumstance that would impede ability to give
informed consent or adherence to study requirements.



Age minimum: 5 Years
Age maximum: 21 Years
Gender: All
Health Condition(s) or Problem(s) studied
Childhood Cancer
Intervention(s)
Behavioral: Multimodal Exercise Intervention
Primary Outcome(s)
Feasibility after 6 month [Time Frame: after primary treatment (6 month)]
Secondary Outcome(s)
Feasibility between 6 and 12 month [Time Frame: between end of primary treatment (6 month) and one year]
Physical performance [Time Frame: after primary treatment (6 month) and after one year]
Quality of Life [Time Frame: after primary treatment (6 month) and after one year]
Secondary ID(s)
S105-2011
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
University Hospital Heidelberg
Children's Medical Hospital, University of Leipzig, Leipzig, Germany
Heidelberg University
University of Leipzig
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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