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Effects of a Supervised Progressive Resistance Training With Breast Cancer Patients During Adjuvant Radiotherapy - A Randomised Controlled Intervention Trial


N/A
18 Years
N/A
Open (Enrolling)
Female
Breast Cancer, Cancer-related Fatigue

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Trial Information

Effects of a Supervised Progressive Resistance Training With Breast Cancer Patients During Adjuvant Radiotherapy - A Randomised Controlled Intervention Trial


Inclusion Criteria:



- histologically confirmed primary breast cancer, stage I-III, after lumpectomy or
mastectomy, indication for adjuvant radiotherapy

- BMI: 18-40

- ability to understand and follow the study protocol

Exclusion Criteria:

- contraindication for exercise

- participation in the BEATE trial or another systematic resistance or relaxation
training

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Outcome Measure:

Fatigue measured by Fatigue Assessment Questionnaire (FAQ)

Outcome Time Frame:

change between baseline and week 13 (end of intervention)

Safety Issue:

No

Principal Investigator

Karen Steindorf, Prof. Dr.

Investigator Role:

Principal Investigator

Investigator Affiliation:

German Cancer Research Center

Authority:

Germany: Ethics Commission

Study ID:

BEST

NCT ID:

NCT01468766

Start Date:

February 2011

Completion Date:

June 2014

Related Keywords:

  • Breast Cancer
  • Cancer-Related Fatigue
  • Breast Neoplasms
  • Fatigue

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