Smart Phone Application in Increasing Physical Activity in Breast Cancer Survivors

Breast Cancer Clinical Trial

Official title:

Facilitating Motivational Readiness and Adoption of Physical Activity by Breast Cancer Survivors With a Smart Phone Application

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03054025
• Other study ID #: 15G.393
• Status: Terminated
• Phase: N/A
• Start date: September 2, 2015
• Est. completion date: May 17, 2018

Study information

• Verified date: October 2019
• Source: Thomas Jefferson University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 22
• Est. completion date: May 17, 2018
• Est. primary completion date: August 31, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: N/A and older

Eligibility

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

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Device:
• Smart Phone Monitoring Device
Use activity tracker application

Locations

Country	Name	City	State
United States	Sidney Kimmel Cancer Center at Thomas Jefferson University	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Sidney Kimmel Cancer Center at Thomas Jefferson University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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

External Links

•   Sidney Kimmel Cancer Center
•   Thomas Jefferson University Hospital