Effects of a Supervised Progressive Resistance Training With Breast Cancer Patients During Adjuvant Radiotherapy - A Randomised Controlled Intervention Trial
Interventional
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Fatigue measured by Fatigue Assessment Questionnaire (FAQ)
change between baseline and week 13 (end of intervention)
No
Karen Steindorf, Prof. Dr.
Principal Investigator
German Cancer Research Center
Germany: Ethics Commission
BEST
NCT01468766
February 2011
June 2014
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