Skip to content

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

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03054025
Enrollment
22
Registered
2017-02-15
Start date
2015-09-02
Completion date
2018-05-17
Last updated
2025-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

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.

Detailed description

PRIMARY OBJECTIVES: I. To conduct a pilot study to inform the design of a mobile health application for smartphone that is targeted to increase physical activity and reduce risks associated with breast cancer.

Interventions

DEVICESmart Phone Monitoring Device

Use activity tracker application

Sponsors

Sidney Kimmel Cancer Center at Thomas Jefferson University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* 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)

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Features of the mobile application that were most used by participants3 weeksDescriptive statistics using proportions and 90% confidence intervals will be calculated for various features.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026