search
Back to results

The Effect of Walking on Fatigue During Radiotherapy in Breast Cancer Patients 65 and Older (WWE)

Primary Purpose

Breast Cancer, Fatigue

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Walk With Ease Arm A
Sponsored by
The West Clinic, Memphis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Cancer

Eligibility Criteria

65 Years - undefined (Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥65 years of age
  • Histologically confirmed Stage I, II or III breast cancer status post breast surgery with or without adjuvant chemotherapy.
  • Scheduled to undergo hypofractionated or standard fractionated radiation therapy to the breast or chest wall.
  • English speaking.
  • IRB approved, signed written informed consent.
  • Approval from their treating radiation oncologist to engage in moderate-intensity physical activity. This will be obtained by the study research coordinator and documented on the study screening form (attached).
  • Patient-assessed ability to walk and engage in moderate physical activity Willing and able to meet all study requirements.

Exclusion Criteria:

  • One or more significant medical conditions that in the physician's judgment preclude participation in the walking intervention.
  • Receiving accelerated partial breast irradiation.
  • Unable to walk or engage in moderate-intensity physical activity.
  • Already participated in Walk with Ease Program.
  • Already actively walking (≥120 minutes per week).

Sites / Locations

  • UNC Lineberger Comprehensive Cancer Center
  • The West Clinic/ University of Tennesee West Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Arm A

Arm B

Arm Description

Women randomized to the WWE program will receive a workbook, and a daily walking log, the latter to be completed during the study.

Patients randomized to the usual care arm will receive a document with information on exercise to improve fatigue during radiotherapy

Outcomes

Primary Outcome Measures

Compare the change in treatment related fatigue from baseline to last week of radiotherapy between patients in the WWE intervention and usual care arms using the Fatigue Symptom Index (FSI).
change in fatigue index

Secondary Outcome Measures

Compare the change in treatment related fatigue from baseline to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the FSI.
change in fatigue index
Change in Treatment Related Fatigue Symptom Index
Compare the change in treatment related fatigue from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the PROMIS Fatigue 8a scale.
Change in Physical Funcionality Index
Compare the change in physical functionality from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the Short Physical Performance Battery and PROMIS Short Form v1.0

Full Information

First Posted
April 20, 2015
Last Updated
December 12, 2017
Sponsor
The West Clinic, Memphis
Collaborators
University of Tennessee West Cancer Center
search

1. Study Identification

Unique Protocol Identification Number
NCT02434367
Brief Title
The Effect of Walking on Fatigue During Radiotherapy in Breast Cancer Patients 65 and Older
Acronym
WWE
Official Title
Phase 2 Randomized Study of a Walking Intervention for Radiation-related Fatigue Among Breast Cancer Patients Receiving Adjuvant Radiation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
August 2014 (Actual)
Primary Completion Date
June 30, 2017 (Actual)
Study Completion Date
June 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The West Clinic, Memphis
Collaborators
University of Tennessee West Cancer Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This multicenter randomized (1:1) phase 2 study is designed to assess the efficacy of the Walk with Ease exercise program on improving fatigue after adjuvant radiotherapy compared to usual care in 50 women with stage 0-3 breast cancer who have undergone breast surgery. Prior to initiation of radiation, during the last week, and 4-6 weeks post radiation, women in both arms will complete a number of surveys including questionnaires on fatigue, pain, depression, sleep, and social support. In addition, a blood sample will be collected prior to, during the last week of radiation, and 4-6 weeks post radiation to explore measures of inflammatory biomarkers, and their potential association with exercise and fatigue.
Detailed Description
Recruitment, consent, and randomization will occur at first postoperative visit with a radiation oncologist. A 1:1 randomization will occur between WWE program and usual care (scripted discussion on benefit of exercise during radiotherapy). Prior to initiation of radiation, women in both arms will complete 68 questions from questionnaires on pain, depression, sleep, and social support. In addition, peripheral blood will be drawn for analysis of pre-radiation measures of inflammatory biomarkers. Women randomized to the WWE program will also receive a daily walking log that they will be asked to fill out and return on the last week of radiation (6 weeks for standard fractionation and 4.5 weeks for hypofractionation), and at 4-6 weeks post radiotherapy. Also, on their last week of radiotherapy and 4-6 weeks after radiotherapy all patients will repeat the questionnaires and a blood draw for measures of inflammatory biomarkers. Contact with study participants will be at 3 points in time after enrollment and randomization: Baseline: At this meeting, requirements of the study will be reviewed, and study materials provided (for control arm: a one page explanation discussing the potential benefits of exercise on fatigue, for experimental arm: WWE workbook, and printed walking log). Participants will complete questionnaires and undergo other assessments including a blood draw. For those on the experimental arm, they will be asked to begin the walking program within a week, noting their walking experience in their daily log. Last week of radiation: All participants will repeat questionnaires and other assessments during any day of their last week of radiation. A repeat blood draw will be taken. In addition those on the WWE arm will have their walking log reviewed. For those receiving hypofractionated radiotherapy, this will occur at week 4. For those receiving standard fractionation this will occur at week 6. 4-6 weeks following end of radiation: All participants will repeat questionnaires and other assessments. A repeat blood draw will be taken. In addition those on the WWE arm will have their walking log reviewed. Patients randomized to the usual care arm will receive a document with information on exercise to improve fatigue during radiotherapy. The sheet will summarize the findings of the 3 randomized studies on exercise intervention during radiotherapy. The primary activity required of study subjects is a 4-6-week self-directed (non-group) WWE walking program that participants do at a place and time that is convenient for them. Participants are asked to walk at a safe and comfortable pace, increasing their minutes per day at a rate they can sustain, with the ultimate goal of 30 minutes/day for at least 5 days/week. They are asked to maintain a daily walking log that is provided to them, entering total minutes per day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Fatigue
Keywords
Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A
Arm Type
Experimental
Arm Description
Women randomized to the WWE program will receive a workbook, and a daily walking log, the latter to be completed during the study.
Arm Title
Arm B
Arm Type
No Intervention
Arm Description
Patients randomized to the usual care arm will receive a document with information on exercise to improve fatigue during radiotherapy
Intervention Type
Behavioral
Intervention Name(s)
Walk With Ease Arm A
Other Intervention Name(s)
WWE
Intervention Description
Walk With Ease is the Arthritis Foundation's evidence-based walking intervention to help with fatigue and pain. The interention is a self directed program that helps guide participants in a safe and comfortable paced walking program with an ultimate goal of walking for 30 minutes per day, five days per week.
Primary Outcome Measure Information:
Title
Compare the change in treatment related fatigue from baseline to last week of radiotherapy between patients in the WWE intervention and usual care arms using the Fatigue Symptom Index (FSI).
Description
change in fatigue index
Time Frame
Four months
Secondary Outcome Measure Information:
Title
Compare the change in treatment related fatigue from baseline to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the FSI.
Description
change in fatigue index
Time Frame
Four months
Title
Change in Treatment Related Fatigue Symptom Index
Description
Compare the change in treatment related fatigue from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the PROMIS Fatigue 8a scale.
Time Frame
Four months
Title
Change in Physical Funcionality Index
Description
Compare the change in physical functionality from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms using the Short Physical Performance Battery and PROMIS Short Form v1.0
Time Frame
Four months
Other Pre-specified Outcome Measures:
Title
Change in Pro-Inflammatory Cytokines
Description
Explore the association between pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6) at baseline, last week of radiation, and 1-4 months after radiation and changes in fatigue and exercise during those time periods. We will assess both the association of cycle.
Time Frame
Four months
Title
Compare the change in fatigue-related side effects from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy between patients in the WWE intervention and usual care arms.
Description
change in fatigue index
Time Frame
Four months
Title
Explore the association between the change in fatigue-related side effects from baseline to last week of radiotherapy and to 1-4 months post-radiotherapy with the change in fatigue at the same time-points.
Description
change in fatigue index
Time Frame
Four months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥65 years of age Histologically confirmed Stage I, II or III breast cancer status post breast surgery with or without adjuvant chemotherapy. Scheduled to undergo hypofractionated or standard fractionated radiation therapy to the breast or chest wall. English speaking. IRB approved, signed written informed consent. Approval from their treating radiation oncologist to engage in moderate-intensity physical activity. This will be obtained by the study research coordinator and documented on the study screening form (attached). Patient-assessed ability to walk and engage in moderate physical activity Willing and able to meet all study requirements. Exclusion Criteria: One or more significant medical conditions that in the physician's judgment preclude participation in the walking intervention. Receiving accelerated partial breast irradiation. Unable to walk or engage in moderate-intensity physical activity. Already participated in Walk with Ease Program. Already actively walking (≥120 minutes per week).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noam VanderWalde, MD
Organizational Affiliation
The West Clinic/University of Tennessee West Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
UNC Lineberger Comprehensive Cancer Center
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
The West Clinic/ University of Tennesee West Cancer Center
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38120
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Effect of Walking on Fatigue During Radiotherapy in Breast Cancer Patients 65 and Older

We'll reach out to this number within 24 hrs