Quality of Life in Breast Cancer Patients and Survivors

Breast Neoplasms Clinical Trial

Official title:

Determinants and Correlates of Physical Activity in Breast Cancer Survivors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01272401
• Other study ID #: UIUC_IRB_10085
• Secondary ID: 1F31AG034025-01A
• Status: Completed
• Phase: N/A
• First received: July 2, 2010
• Last updated: February 21, 2017
• Start date: June 2010
• Est. completion date: May 2011

Study information

• Verified date: February 2017
• Source: University of Illinois at Urbana-Champaign
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 500
• Est. completion date: May 2011
• Est. primary completion date: May 2011
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Breast Neoplasms

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
University of Illinois at Urbana-Champaign	National Institute on Aging (NIA)

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quality of life. Health-related quality of life will be assessed utilizing a breast cancer specific quality of life measure and global quality of life will be assessed using the satisfaction with life scale.		Baseline
Primary	Quality of life. Health-related quality of life will be assessed utilizing a breast cancer specific quality of life measure and global quality of life will be assessed using the satisfaction with life scale.		6 months
Secondary	Self-efficacy for engaging in physical activity and overcoming barriers to physical activity.		Baseline
Secondary	Physical activity as measured by questionnaire and 7 day accelerometry.		Baseline
Secondary	Self-efficacy for engaging in physical activity and overcoming barriers to physical activity.		6 months
Secondary	Physical activity as measured by questionnaire and 7 day accelerometry.		6 months