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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02559362
Other study ID # UPCC 23114
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2015
Est. completion date June 3, 2016

Study information

Verified date April 2020
Source Abramson Cancer Center of the University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date June 3, 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- women,

- breast cancer diagnosis,

- all races will be included.

Exclusion Criteria:

- men,

- those with no breast cancer (ductal carcinoma in situ),

- pregnant women,

- children

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Survey


Locations

Country Name City State
United States Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Abramson Cancer Center of the University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of subjects providing completed surveys 1 year
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