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Physical Activity Program for Breast Cancer (MFT4 Trial)
N/A
Waitlist Available
Led By Bernardine M. Pinto, PhD
Research Sponsored by University of South Carolina
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Ambulatory
Able to walk unassisted
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-month intervention
Awards & highlights
Summary
This trialwill measure effects of a 3-month physical activity intervention on breast cancer survivors not currently active. A web-based platform and virtual calls with a peer coach will be used to increase activity. Participants will be given a Fitbit to monitor activity.
Who is the study for?
This trial is for breast cancer survivors diagnosed within the last 5 years, who are currently inactive. They should be able to walk unassisted, read and speak English, and have access to a smartphone with Bluetooth and internet. Participants must not engage in more than 30 minutes of vigorous or 90 minutes of moderate-intensity physical activity weekly.
What is being tested?
The study tests if guidance from a peer coach can help increase moderate-intensity physical activity over three months compared to self-monitoring. Participants will be randomly placed into two groups: one receiving weekly virtual coaching and the other monitoring their own activity levels. Both groups get a Fitbit.
What are the potential side effects?
Since this trial involves increasing physical activity, potential side effects may include muscle soreness, fatigue, or injury due to exercise. However, these risks are generally low as activities are moderate in intensity.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can walk on my own without help.
Select...
I can walk by myself without help.
Select...
I was diagnosed with Stage 0-3 breast cancer in the last 5 years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-month intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-month intervention
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Accelerometer measured moderate-to-vigorous activity
Secondary study objectives
Self-Reported Fatigue
Self-Reported Mood
Self-Reported Physical Functioning
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: webMFTExperimental Treatment1 Intervention
Survivors randomized to webMFT will receive the evidence-based intervention for moderate-to-vigorous physical activity (MVPA) promotion that consists of MVPA counseling matched to patients' motivational readiness, and self-monitoring of MVPA (via Fitbit Inspire 2). The goal for the 3-month program will be to gradually increase the amount of moderate-intensity aerobic exercise that is performed, to the current national recommendations of at least 150 minutes of MPVA per week. Our goal is to promote aerobic exercise that is safe and enjoyable, such as walking.
Group II: MVPA trackingActive Control1 Intervention
These survivors will be asked to self-monitor moderate-to-vigorous physical activity (MVPA) participation by wearing the Fitbit Inspire 2 each day over 12 weeks. This group will not receive the MVPA counseling from the coaches.
Find a Location
Who is running the clinical trial?
University of Colorado, DenverOTHER
1,786 Previous Clinical Trials
2,787,540 Total Patients Enrolled
29 Trials studying Breast Cancer
6,821 Patients Enrolled for Breast Cancer
University of South CarolinaLead Sponsor
217 Previous Clinical Trials
121,297 Total Patients Enrolled
4 Trials studying Breast Cancer
763 Patients Enrolled for Breast Cancer
InquisitHealth, Inc.OTHER
2 Previous Clinical Trials
336 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I was diagnosed with Stage 0-3 breast cancer in the last 5 years.I can walk on my own without help.I can walk by myself without help.
Research Study Groups:
This trial has the following groups:- Group 1: MVPA tracking
- Group 2: webMFT
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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