Study Results
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View full resultsBasic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2020-05-11
2022-03-29
Brief Summary
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The goal of this study is to compare an intervention that uses active games versus an intervention uses pedometer to encourage physical activity such as walking within breast cancer survivors in active cancer treatment. The study will include breast cancer survivor between the ages of 18 - 70 whom currently gets less than 150 minutes of planned physical activity per week and received a breast cancer diagnosis within 0 to 6 months. Participants will be randomized to participate in the support group using the active video game-based physical activity intervention (Wii and Xbox active games) or to participate in the existing UTMB breast cancer support group with pedometers (Digi-Walker CW-700/701). The investigators hypothesize that by engaging in active video gaming, breast cancer survivors will be motivated to initiate and maintain physical activity during treatment. This will ultimately increase functional capacity and prevent functional disability in breast cancer survivors.
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Detailed Description
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Aim 1: Evaluate the feasibility and acceptability of active video game-based physical activity intervention among BC survivors undergoing treatment within the support group setting. Measures of feasibility will include weekly attendance records, number of completed home-based worksheets, number of participants completing the program activities, technological issues, and adverse events.
Aim 2: Compare the support group using the active video game-based physical activity intervention to the existing UTMB breast cancer support group with pedometer. Primary outcomes will be changes in physical activity. Secondary outcomes will be changes in physical function, dietary pattern, and quality of life.
Aim 3: Develop tools for implementation of the Pink Warrior intervention within the clinic and community settings. A trainer's manual for the Pink Warrior intervention will be developed and UTMB Breast Cancer Support Group facilitators will be trained by research staff to implement the program.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Active video game teleconference support group
Participants will attend enhanced support group meetings via zoom teleconferencing software. Support group meetings will include group play of active video games and discussion of survivorship topics. Participants will self-monitor physical activity using Fitbit wearable activity monitors and will receive a water bottle and tote bag.
Active video game teleconference support group
12 sessions of teleconferenced support group meetings, including active video game play + self-paced walking monitored by Fitbit wearable device
Standard support group + pedometer
Participants will attend standard in-person support groups currently offered by the UTMB Breast Health Center. They will also receive a standard pedometer and a water bottle and tote bag.
Standard support group + pedometer
3 monthly sessions of in-person standard support group meetings + self-paced walking monitored by pedometer
Interventions
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Active video game teleconference support group
12 sessions of teleconferenced support group meetings, including active video game play + self-paced walking monitored by Fitbit wearable device
Standard support group + pedometer
3 monthly sessions of in-person standard support group meetings + self-paced walking monitored by pedometer
Eligibility Criteria
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Inclusion Criteria
2. Diagnosed with primary female breast cancer
3. 55 years to 79
4. Able to speak, read, and write in English
5. Able to travel to UTMB locations and/or MD Anderson Victory Lakes
6. Able to move arms and les as well as ambulate
7. Has a smartphone, tablet or computer and daily access to a reliable internet
Exclusion Criteria
2. Diagnosed dementia
3. Currently engage in 150 minutes or more of planned moderate intensity physical activity
4. Currently involved in another physical activity intervention
55 Years
79 Years
FEMALE
No
Sponsors
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M.D. Anderson Cancer Center
OTHER
National Institute on Aging (NIA)
NIH
The University of Texas Medical Branch, Galveston
OTHER
Responsible Party
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Principal Investigators
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Elizabeth J Lyons, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
University of Texas
Locations
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The University of Texas Medical Branch
Galveston, Texas, United States
UT MD Anderson Cancer Center
Houston, Texas, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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16-0040-02
Identifier Type: -
Identifier Source: org_study_id
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