Optimization of Remotely Delivered Physical Activity Intervention for Breast Cancer Survivors



Status:Active, not recruiting
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:3/28/2019
Start Date:April 24, 2017
End Date:July 31, 2020

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Designing With Dissemination in Mind: Optimization of a mHealth Physical Activity Intervention for Breast Cancer Survivors

The overall objective of the proposed research is to pilot test the feasibility and
acceptability of a set of more scalable technology-supported physical activity promotion
intervention strategies in breast cancer survivors using tMultiphase Optimization Strategy
Trial (MOST) methodology. MOST involves highly efficient randomized experimentation to assess
the effects of individual intervention strategies, and thereby identify which strategies and
what strategy levels make the important contributions to the overall program's effect on
physical activity. This information then guides assembly of an optimized physical activity
program, that achieves target outcomes with least resource consumption and participant
burden. The resulting intervention will have great potential for scalability because it uses
technology (smartphones) participants already own and requires no on-site visits.


Inclusion Criteria:

1. Diagnosed with Stage I-III breast cancer within the last 5 years

2. Have completed last cancer treatment (adjuvant chemotherapy, radiation therapy or
surgery) at least 3 months prior to enrollment

3. English speaking

4. Currently participate in less than 60 minutes of moderate and vigorous physical
activity per week

5. Own a smartphone

6. Have access to a computer with Internet

7. Participants may be using adjuvant endocrine therapies.

8. Willing to be waitlisted for future wave if current wave reaches capacity

Exclusion Criteria:

-Women will be excluded if they report any of the following:

1. Respiratory, joint or cardiovascular problems precluding physical activity

2. Metastatic disease

3. Planned elective surgery during duration of the intervention/follow-up that would
interfere with participation (e.g., breast reconstructive surgery).

ONLY IF PARTICIPATING IN OPTIONAL BLOOD COLLECTION:

1. A prior cardiovascular event (i.e. stroke, myocardial infarction)

2. Have been diagnosed with an acute or chronic immune system medical conditions, or
conditions that impact immune and endocrine function (e.g., CFS, Lupus, rheumatoid
arthritis, Hepatitis C, or immunosuppressive treatment requiring conditions)
We found this trial at
1
site
303 East Superior Street
Chicago, Illinois 60611
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from
Chicago, IL
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