Study Stopped
funding discontinued
Smart Phone Application in Increasing Physical Activity in Breast Cancer Survivors
Facilitating Motivational Readiness and Adoption of Physical Activity by Breast Cancer Survivors With a Smart Phone Application
2 other identifiers
interventional
22
1 country
1
Brief Summary
This pilot clinical trial studies how well a smart phone application works in increasing physical activity in breast cancer survivors. A smart phone application that increases physical activity may help reduce the likelihood of cancer coming back in breast cancer survivors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable breast-cancer
Started Sep 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 2, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2016
CompletedFirst Submitted
Initial submission to the registry
January 31, 2017
CompletedFirst Posted
Study publicly available on registry
February 15, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
May 17, 2018
CompletedApril 29, 2025
April 1, 2025
12 months
January 31, 2017
April 28, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Features of the mobile application that were most used by participants
Descriptive statistics using proportions and 90% confidence intervals will be calculated for various features.
3 weeks
Study Arms (1)
Supportive care (smart phone application)
EXPERIMENTALParticipants download the physical activity readiness smart phone application onto their personal smartphone and receive training on how to use the app which includes animated video clips, tailored email reminders, and feedback on progress for 3 weeks.
Interventions
Use activity tracker application
Eligibility Criteria
You may qualify if:
- A participant is only able to participate in one phase, not both phases, of the research study
- Must have completed breast cancer treatment
- Those on adjuvant hormonal therapy are allowed to participate in the research study (either phase)
You may not qualify if:
- Those who currently meet the Centers for Disease Control and Prevention (CDC)'s physical activity guidelines
- Those who do not currently use a smartphone (of any kind)
- Those who do not read and speak English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sidney Kimmel Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Andrea Barsevick, PhD
Sidney Kimmel Cancer Center at Thomas Jefferson University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 31, 2017
First Posted
February 15, 2017
Study Start
September 2, 2015
Primary Completion
August 31, 2016
Study Completion
May 17, 2018
Last Updated
April 29, 2025
Record last verified: 2025-04