Effects of a Supervised Progressive Resistance Training With Breast Cancer Patients During Adjuvant Radiotherapy - A Randomised Controlled Intervention Trial
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)
Karen Steindorf, Prof. Dr.
German Cancer Research Center
Germany: Ethics Commission