Physical Activity Program for Breast Cancer Survivors

Pilot SMART of a Remotely Delivered, Adaptive Physical Activity Intervention for Breast Cancer Survivors

Recruiting N/A Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
55 (estimated)
Sponsor
Dartmouth-Hitchcock Medical Center · Other
Who this trial is looking for

This trial is looking for breast cancer survivors who want to increase their physical activity. Participants will meet with an exercise specialist and wear an activity monitor to track their progress.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am 18 years or older.
  • I have completed primary cancer treatment for Stage 0-III breast cancer within the last 5 years.
  • I currently do less than 60 minutes of moderate-vigorous physical activity each week.
  • I own a smartphone or tablet and can use it for surveys.
  • I can wear an activity monitor during the study.
  • I have access to the internet for surveys.

You may not be able to join if

  • I do not speak or read English.
  • I have major health issues that prevent me from exercising.
  • I am currently pregnant.
  • I have a history of severe mental illness or take certain mood medications.
  • I have moderate to severe depressive symptoms.
  • I have moderate to severe cognitive impairment.
  • I have clinically significant substance use issues.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The goal of this clinical trial is to evaluate the feasibility of randomizing participants to a "step-up" intervention pathway when they perform \<150 minutes of MVPA at the 6-week data collection burst. Participants who performed \<150 minutes of MVPA at the 6-week data collection burst will be randomized to either continue with the standard intervention or advance to the step-up intervention. Th…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: -≥18 years old * Within 5 years of completing primary cancer treatment (surgery, chemotherapy, and radiation) for Stage 0-III breast cancer * \<60 mins/week moderate-vigorous physical activity (MVPA) with no major changes for the past 6- months * Own an Android or iPhone smartp…
Contacts

Courtney J Stevens, PhD

6036509643

courtney.j.stevens@dartmouth.edu

CONTACT

Aislinn Mitcham, BA

6036466545

aislinn.e.mitcham@hitchcock.org

CONTACT