Main
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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:
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ClinicalTrials.gov |
Last refreshed on:
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12 December 2020 |
Main ID: |
NCT02216604 |
Date of registration:
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13/08/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Exercise in Pediatric Cancer Patient Undergoing Anti-Cancer Treatment
ONKOKIDS-HD |
Scientific title:
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Physical Activity Intervention Program for Childhood Cancer Patients Under Chemo- and/or Radiation Therapy |
Date of first enrolment:
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May 2011 |
Target sample size:
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50 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02216604 |
Study type:
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Interventional |
Study design:
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Allocation: Non-Randomized. Intervention model: Factorial Assignment. Primary purpose: Supportive Care. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Germany
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Contacts
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Name:
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Joachim Wiskemann, PhD |
Address:
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Telephone:
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Email:
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Affiliation:
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National Center for Tumor Diseases |
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Key inclusion & exclusion criteria
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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
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Health Condition(s) or Problem(s) studied
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Childhood Cancer
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Intervention(s)
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Behavioral: Multimodal Exercise Intervention
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Primary Outcome(s)
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Feasibility after 6 month
[Time Frame: after primary treatment (6 month)]
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Secondary Outcome(s)
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Feasibility between 6 and 12 month
[Time Frame: between end of primary treatment (6 month) and one year]
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Physical performance
[Time Frame: after primary treatment (6 month) and after one year]
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Quality of Life
[Time Frame: after primary treatment (6 month) and after one year]
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Secondary ID(s)
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S105-2011
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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