NCT02559362

Brief Summary

The goal of the study is to establish the feasibility/willingness of breast cancer patients to delay surgery to do an exercise program, or be randomized to an exercise training program following treatment, and to see if that willingness correlates with prior physical activity history.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2015

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2015

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 19, 2015

Completed
3 months until next milestone

First Posted

Study publicly available on registry

September 24, 2015

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2016

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 3, 2016

Completed
Last Updated

April 9, 2020

Status Verified

April 1, 2020

Enrollment Period

1.2 years

First QC Date

June 19, 2015

Last Update Submit

April 7, 2020

Conditions

Breast Cancer

Outcome Measures

Primary Outcomes (1)

  • Number of subjects providing completed surveys

    1 year

Interventions

SurveyBEHAVIORAL

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Breast cancer subjects

You may qualify if:

  • women,
  • breast cancer diagnosis,
  • all races will be included.

You may not qualify if:

  • men,
  • those with no breast cancer (ductal carcinoma in situ),
  • pregnant women,
  • children

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Abramson Cancer Center of the University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

Location

MeSH Terms

Conditions

Breast Neoplasms

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Kathryn Schmitz, PhD

    Abramson Cancer Center at Penn Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 19, 2015

First Posted

September 24, 2015

Study Start

April 1, 2015

Primary Completion

June 1, 2016

Study Completion

June 3, 2016

Last Updated

April 9, 2020

Record last verified: 2020-04

Locations

US(1)