Clinical Trials Directory

Trials / Completed

CompletedNCT01468766

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (actual)
Sponsor
German Cancer Research Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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

TypeNameDescription
OTHERSupervised progressive resistance training2x60 minutes per week for 12 weeks
OTHERSupervised progressive muscle relaxation training (Jacobson method)2x60 minutes per week for 12 weeks

Timeline

Start date
2011-02-01
Primary completion
2013-07-01
Completion
2014-07-01
First posted
2011-11-09
Last updated
2016-04-19

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01468766. Inclusion in this directory is not an endorsement.