Aerobic and Strength Training Exercise in Improving Fitness and Arm Health During and After Radiation Therapy in Patients With Stage II-III Breast Cancer
Primary Purpose
Stage II Breast Cancer, Stage IIA Breast Cancer, Stage IIB Breast Cancer
Status
Suspended
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Best Practice
Exercise Intervention
Quality-of-Life Assessment
Questionnaire Administration
Sponsored by

About this trial
This is an interventional supportive care trial for Stage II Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Stage II-III breast cancer
- Prior surgery including lumpectomy or mastectomy and sentinel node biopsy or axillary lymph node dissection
- Prior chemotherapy in the neoadjuvant or adjuvant setting
- Radiation plan consisting of regional nodal radiation
- Must be suitable for an exercise program
Exclusion Criteria:
- Serious underlying medical comorbidity such as uncontrolled hypertension, cardiovascular disease, pulmonary disease, psychiatric illness, or any other condition for which the patient is not approved for exercise by their physician
- Physical handicap that would prevent participation in program
- Patients with metastatic breast cancer
Sites / Locations
- Ohio State University Comprehensive Cancer Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Arm I (usual care)
Arm II (aerobic and strength training exercise)
Arm Description
Patients receive usual care for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
Patients undergo a supervised aerobic and strength training exercise session over 40-60 minutes 3 times weekly for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
Outcomes
Primary Outcome Measures
Number of participants who complete 70% of all exercise sessions throughout the supervised program during and after radiation therapy (Pilot)
determine the feasibility of conducting an exercise program during and after radiation therapy and to determine what percent of patients will complete the exercise program.
Percent increase in fitness as measured by the 6 minute walk test in patients randomized to exercise program (Phase II)
Will be compared to usual care group.
Secondary Outcome Measures
Arm lymphedema as measured by arm circumference
Lymphedema will be classified into 3 stages. Stage I edema is reversible and characterized by pitting edema, increase in arm girth, and heaviness. Stage II is characterized by a spongy consistency of the arm without pitting edema. Stage III is the most advanced stage, lymphostatic elephantiasis
Arm range of motion as measured by goniometry
Shoulder flexion, external and internal rotation, and abduction will be measured.
Change in weight and BMI
BMI will be measured to evaluate body composition using the metric formula weight (kg)/ height 2 (m2).
Percent adherence to exercise as measured by the International Physical Activity Questionnaire and exercise logs
Duration of exercise will be calculated based on questionnaire and exercise log. Percentage of exercise adherence at 1-year follow-up will be compared between two groups. Generalized linear models will be utilized to model follow-up as a function of baseline and group.
Percent increase in arm strength as measured by one repetition maximum
Change in strength from baseline to post-intervention and follow-up will be obtained.
Quality of life as measured by FACT-B+4
The FACT B + 4 has been shown to have good internal consistency and stability. It is a 40 item Likert scale questionnaire with subscales (0 - 4) for physical well being, social/family well being, emotional well being, function well being, and 4 specific questions related to arm symptoms.
Subjective arm health as measured by FACT-B+4
The FACT B + 4 has been shown to have good internal consistency and stability. It is a 40 item Likert scale questionnaire with subscales (0 - 4) for physical well being, social/family well being, emotional well being, function well being, and 4 specific questions related to arm symptoms.
Full Information
NCT ID
NCT03102866
First Posted
March 20, 2017
Last Updated
April 3, 2023
Sponsor
Ohio State University Comprehensive Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT03102866
Brief Title
Aerobic and Strength Training Exercise in Improving Fitness and Arm Health During and After Radiation Therapy in Patients With Stage II-III Breast Cancer
Official Title
Can Aerobic and Strength Training Exercise Initiated During and Continued After Radiation Therapy for Breast Cancer Improve Fitness and Arm Health 1 Year Later?
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Suspended
Why Stopped
Internal data analysis
Study Start Date
August 30, 2017 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University Comprehensive Cancer Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This randomized pilot phase I/II trial studies how well aerobic and strength training exercise works in improving fitness and arm health during and after radiation therapy consisting of regional nodal radiation in patients with stage II-III breast cancer. Aerobic and strength training exercise training during and after radiation therapy may reduce treatment related toxicities and improve adherence to exercise long term in patients with breast cancer.
Detailed Description
PRIMARY OBJECTIVES:
I. To determine the feasibility of conducting an exercise program during and after radiation therapy and to determine what percent of patients will complete the exercise program. (Pilot) II. To determine the percent increase in fitness as measured by the 6 minute walk test in women receiving radiation therapy for breast cancer randomized to an exercise program at 1 year. (Phase II)
SECONDARY OBJECTIVES:
I. Percent adherence to exercise at 1 year as measured by the International Physical Activity Questionnaire and exercise logs.
II. Subjective arm health at 1 year as measured by Functional Assessment of Cancer Therapy Questionnaire for Breast Cancer version 4 (FACT-B+4).
III. Arm lymphedema at 1 year as measured by arm circumference. IV. Arm range of motion at 1 year as measured by goniometry. V. Quality of life at 1 year as measured by FACT-B+4. VI. Percent increase in arm strength as measured by one repetition maximum at 1 year.
VII. Change in weight and body mass index (BMI) 1 year after completion of radiation.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM I: Patients receive usual care for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
ARM II: Patients undergo a supervised aerobic and strength training exercise session over 40-60 minutes 3 times weekly for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
After completion of study, patients are followed up at 1 year.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stage II Breast Cancer, Stage IIA Breast Cancer, Stage IIB Breast Cancer, Stage III Breast Cancer, Stage IIIA Breast Cancer, Stage IIIB Breast Cancer, Stage IIIC Breast Cancer
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm I (usual care)
Arm Type
Active Comparator
Arm Description
Patients receive usual care for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
Arm Title
Arm II (aerobic and strength training exercise)
Arm Type
Experimental
Arm Description
Patients undergo a supervised aerobic and strength training exercise session over 40-60 minutes 3 times weekly for 6 weeks during radiation therapy and for 12 weeks after completion of radiation therapy.
Intervention Type
Other
Intervention Name(s)
Best Practice
Other Intervention Name(s)
standard of care, standard therapy
Intervention Description
Receive usual care
Intervention Type
Behavioral
Intervention Name(s)
Exercise Intervention
Intervention Description
Undergo aerobic and strength training exercise
Intervention Type
Other
Intervention Name(s)
Quality-of-Life Assessment
Other Intervention Name(s)
Quality of Life Assessment
Intervention Description
Ancillary studies
Intervention Type
Other
Intervention Name(s)
Questionnaire Administration
Intervention Description
Ancillary studies
Primary Outcome Measure Information:
Title
Number of participants who complete 70% of all exercise sessions throughout the supervised program during and after radiation therapy (Pilot)
Description
determine the feasibility of conducting an exercise program during and after radiation therapy and to determine what percent of patients will complete the exercise program.
Time Frame
Up to 1 year
Title
Percent increase in fitness as measured by the 6 minute walk test in patients randomized to exercise program (Phase II)
Description
Will be compared to usual care group.
Time Frame
At 1 year
Secondary Outcome Measure Information:
Title
Arm lymphedema as measured by arm circumference
Description
Lymphedema will be classified into 3 stages. Stage I edema is reversible and characterized by pitting edema, increase in arm girth, and heaviness. Stage II is characterized by a spongy consistency of the arm without pitting edema. Stage III is the most advanced stage, lymphostatic elephantiasis
Time Frame
Baseline up to 1 year
Title
Arm range of motion as measured by goniometry
Description
Shoulder flexion, external and internal rotation, and abduction will be measured.
Time Frame
Baseline up to 1 year
Title
Change in weight and BMI
Description
BMI will be measured to evaluate body composition using the metric formula weight (kg)/ height 2 (m2).
Time Frame
Baseline up to 1 year
Title
Percent adherence to exercise as measured by the International Physical Activity Questionnaire and exercise logs
Description
Duration of exercise will be calculated based on questionnaire and exercise log. Percentage of exercise adherence at 1-year follow-up will be compared between two groups. Generalized linear models will be utilized to model follow-up as a function of baseline and group.
Time Frame
Baseline up to 1 year
Title
Percent increase in arm strength as measured by one repetition maximum
Description
Change in strength from baseline to post-intervention and follow-up will be obtained.
Time Frame
Baseline up to 1 year
Title
Quality of life as measured by FACT-B+4
Description
The FACT B + 4 has been shown to have good internal consistency and stability. It is a 40 item Likert scale questionnaire with subscales (0 - 4) for physical well being, social/family well being, emotional well being, function well being, and 4 specific questions related to arm symptoms.
Time Frame
Baseline up to 1 year
Title
Subjective arm health as measured by FACT-B+4
Description
The FACT B + 4 has been shown to have good internal consistency and stability. It is a 40 item Likert scale questionnaire with subscales (0 - 4) for physical well being, social/family well being, emotional well being, function well being, and 4 specific questions related to arm symptoms.
Time Frame
Baseline up to 1 year
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Stage II-III breast cancer
Prior surgery including lumpectomy or mastectomy and sentinel node biopsy or axillary lymph node dissection
Prior chemotherapy in the neoadjuvant or adjuvant setting
Radiation plan consisting of regional nodal radiation
Must be suitable for an exercise program
Exclusion Criteria:
Serious underlying medical comorbidity such as uncontrolled hypertension, cardiovascular disease, pulmonary disease, psychiatric illness, or any other condition for which the patient is not approved for exercise by their physician
Physical handicap that would prevent participation in program
Patients with metastatic breast cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sasha Beyer, MD
Organizational Affiliation
Ohio State University Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University Comprehensive Cancer Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
http://cancer.osu.edu
Description
The Jamesline
Learn more about this trial
Aerobic and Strength Training Exercise in Improving Fitness and Arm Health During and After Radiation Therapy in Patients With Stage II-III Breast Cancer
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