Quality of Life in Breast Cancer Patients and Survivors

NCT ID: NCT01272401

Last Updated: 2017-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-06-30

Study Completion Date

2011-05-31

Brief Summary

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The purpose of this study is to determine how physical activity, other lifestyle factors, and psychosocial factors are related to quality of life and other health outcomes across the breast cancer survival spectrum from diagnosis to long term survival in a nationally representative sample of breast cancer patients and survivors across a 6 month period of time.

Detailed Description

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Participants in this study will be asked to sign an informed consent, wear an activity monitor (similar to a pedometer) for 7 consecutive days and complete a packet of questionnaires. The questionnaires will take about 45 minutes to complete. All materials will be sent to participants via the US Postal Service and will need to be mailed back in the provided self-addressed stamped envelopes within 2 weeks. Participants will be asked to repeat these same assessments again in 6 months. NO lab visits will be required for participation. Women from all across the U.S. who have been diagnosed with breast cancer at any point in their lives are being sought. There is no limit on time since diagnosis or treatment status.

Conditions

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Breast Neoplasms

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Breast cancer patients and survivors

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Female
* Have received a breast cancer diagnosis and consider self a breast cancer patient or survivor
* Aged 18 years and older
* English speaking
* No limit on time since diagnosis

Exclusion Criteria

* Under the age of 18
* Male
* Have never been diagnosed with breast cancer
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Aging (NIA)

NIH

Sponsor Role collaborator

University of Illinois at Urbana-Champaign

OTHER

Sponsor Role lead

Responsible Party

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Edward McAuley

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Edward McAuley, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Illinois at Urbana-Champaign

Other Identifiers

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1F31AG034025-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

UIUC_IRB_10085

Identifier Type: -

Identifier Source: org_study_id

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