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Smart Phone Application in Increasing Physical Activity in Breast Cancer Survivors

Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University (Other)
Overall Status
Terminated
CT.gov ID
NCT03054025
Collaborator
(none)
22
Enrollment
1
Location
1
Arm
32.5
Actual Duration (Months)
0.7
Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Smart Phone Monitoring Device
 N/A

Detailed Description

PRIMARY OBJECTIVES:
  1. 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Facilitating Motivational Readiness and Adoption of Physical Activity by Breast Cancer Survivors With a Smart Phone Application
Actual Study Start Date :
Sep 2, 2015
Actual Primary Completion Date :
Aug 31, 2016
Actual Study Completion Date :
May 17, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Supportive care (smart phone application)

Participants 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.

Device: Smart Phone Monitoring Device
Use activity tracker application
Other Names:
  • Monitor

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Features of the mobile application that were most used by participants [3 weeks]

      Descriptive statistics using proportions and 90% confidence intervals will be calculated for various features.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sidney Kimmel Cancer Center at Thomas Jefferson University Philadelphia Pennsylvania United States 19107

    Sponsors and Collaborators

    • Sidney Kimmel Cancer Center at Thomas Jefferson University

    Investigators

    • Principal Investigator: Andrea Barsevick, PhD, Sidney Kimmel Cancer Center at Thomas Jefferson University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Sidney Kimmel Cancer Center at Thomas Jefferson University
    ClinicalTrials.gov Identifier:
    NCT03054025
    Other Study ID Numbers:
    • 15G.393
    First Posted:
    Feb 15, 2017
    Last Update Posted:
    Nov 1, 2019
    Last Verified:
    Oct 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Breast Neoplasms

    Study Results

    No Results Posted as of Nov 1, 2019