MedTrace Logo

Effects of a Supervised Progressive Resistance Training With Breast Cancer Patients During Adjuvant Radiotherapy

NCT01468766 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2016-04-19

No results posted yet for this study

Summary

The purpose of this randomized intervention study is to investigate the effects and biological mechanisms of a supervised 12-week progressive resistance training on fatigue and immunological and inflammatory biomarkers in breast cancer patients during adjuvant radiotherapy. To determine the effect of the exercise itself beyond potential psychosocial effects due to attention by trainers or the group support, patients in the control group have a comparable training schedule (i.e. 60 min, twice a week, for 12 weeks) but with relaxation training (Jacobsen method).

Conditions

Interventions

OTHER

Supervised progressive resistance training

2x60 minutes per week for 12 weeks

OTHER

Supervised progressive muscle relaxation training (Jacobson method)

2x60 minutes per week for 12 weeks

Sponsors & Collaborators

  • University Hospital Heidelberg

    collaborator OTHER

  • National Center for Tumor Diseases, Heidelberg

    collaborator OTHER

  • German Cancer Research Center

    lead OTHER

Principal Investigators

  • Karen Steindorf, Prof. Dr. · German Cancer Research Center

  • Karin Potthoff, Dr. · University Hospital Heidelberg

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2013-07-31
Completion
2014-07-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01468766 on ClinicalTrials.gov