Exercise Program of Breast Cancer Patients Undergoing Chemotherapy With or Without Radiation

NCT01157767 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2021-09-01

No results posted yet for this study

Summary

The purpose of this study is to study if a patients follows an exercise program specifically designed for them during the time of their treatment after surgery. Their ability to follow the program and its influence on their weight maintenance and early post-operative lymphedema rates will also be studied. Lymphedema is a condition in which excess fluid collects in tissue and causes swelling of the arm(s).

Conditions

Interventions

OTHER

standardized regimen of exercises, including a warm-up period, ROM arm exercises, and strength training exercises.

Module I is a group of arm movements. It consists of stretching exercises coordinated with breathing exercises to restore their physical mobility, range of motion and flexibility of shoulders. Module I is to be performed daily. In Module II the exercises are a series of copyrighted, sequential movements designed to put the body in proper alignment. It is a special series of muscle movements to help establish better body alignment, as well as increased strength and flexibility of one's arms, legs, and spine, each exercise is 4 repetitions. Module III is the walking and the resistance weight training program. The walking program is whole body exercise, multi-joint, weight-bearing, low impact and for beginners to advanced.

Sponsors & Collaborators

Principal Investigators

  • Alexandra Heerdt, MD, MPH · Memorial Sloan Kettering Cancer Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-11
Primary Completion
2021-08-23
Completion
2021-08-23

Countries

  • United States

Study Locations

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Entities

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 NCT01157767 on ClinicalTrials.gov