NCT04262180Completed
Physical Activity Promotion for Breast and Endometrial Cancer Survivors
Multi-site Adaptive Trial of a Technology-based, EHR-integrated Physical Activity Intervention in Breast and Endometrial Cancer Survivors
Source: ClinicalTrials.gov · Last updated 24 Oct 2025
Brief summary (registry, in English)
Many breast and endometrial cancer survivors do not get enough physical activity. Technology-based interventions can be inexpensive and easy to scale up, however they are not effective for all women. The purpose of this study is test an adaptive physical activity intervention approach that reserves the most resources and support for women who do not fare well with a lower-cost, minimal intervention. The results from this trial will inform the development of scalable physical activity interventions for breast and endometrial cancer survivors.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 323 (actual)
- First submitted
- 6 Feb 2020
- Start date
- 9 Nov 2020
- Primary completion date
- 15 Sept 2025
- Lead sponsor
- University of Wisconsin, Madison
- Diseases
- Endometrial cancer
- NCT number
- NCT04262180
What you commit to
- Study type: Interventional
- Participants enrolled: 323
- From 9 Nov 2020 to the primary completion date, 15 Sept 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Any absolute contraindications to exercise (i.e. acute myocardial infarction, severe orthopedic conditions), metastatic disease or planned elective surgery during intervention/ follow-up.
Other
- Self-reported difficulty transitioning walking 1 block (as a proxy measure of basic physical functioning), or inability to work towards the intervention goals
- Plans to become pregnant or to move from the area within the next two years
- Current enrollment in another dietary or physical activity trial
Who the study is looking for
- Female adult (≥18 years of age)
- Diagnosis of Stage I-III breast or Stage I-II Type 1 endometrial cancer within the past 5 years.
- At least 3 months past completion of primary active treatment (i.e., surgery, chemotherapy, and/or radiation). May still be undergoing endocrine or Human epidermal growth factor receptor 2 (Her2) therapies.
- Insufficiently active, defined as ≤60 min/week of MVPA, performed in bouts of ≥10 minutes.This is 40% of the recommended amount of MVPA based on the 2008 Federal Guidelines and the American Cancer Society's guidelines for cancer survivors. The 7-Day Recall will be used to screen for physical activity; eligibility will be confirmed prior to randomization using the ActiGraph accelerometer.
- Able to access high-speed Internet daily at home on a computer, smartphone, or tablet. Internet access may be through a household connection or a wireless provider (e.g., Verizon, AT\&T). For compatibility with the Fitbit, the device must run a Windows, Apple, or Android operating system.
- Have a MyChart account or be willing to create one.
- Fluent in spoken and written English language.
- For safety, participants will be screened using the Physical Activity Readiness Questionnaire (PAR-Q) and the Falls Risk Screener, which address joint and cardiovascular problems, balance issues, and other concerns. Physician consent will be obtained for all participants who meet the following criteria:
- Answer yes to ≥1 question on the PAR-Q OR
- Answer yes to ≥4 questions on the Falls Risk Screener
- Willing and able to attend study visits at the University of Wisconsin, Madison or Northwestern University, Chicago
- Own and can use a smartphone
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Department of Preventative Medicine, Northwestern University Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Department of Kinesiology, University of Wisconsin Coordinator of this site? Confirm its status | Madison | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.