Breast Cancer Clinical Trial
Official title:
Pain in Cancer Survivors
The purpose of this study is to find out about the pain and quality of life of individuals who are adult cancer survivors. By quality of life, we mean how you are feeling about different aspects of your life, including your physical health, your emotional health, and your ability to carry out daily activities. We are interested in people's opinions about their quality of life, as well as the factors that affect their quality of life. In addition, learning about pain will help us to develop new services for adult cancer survivors.
Status | Completed |
Enrollment | 200 |
Est. completion date | January 2012 |
Est. primary completion date | January 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Cancer treatment at MSKCC - Are from 1 to 10 years post-treatment completion at the time of study recruitment - No evidence of disease (NED) at the time of assessment; - Over 18 years of age - Can be reached by telephone - Able to provide informed consent - Able to speak and read English - Cancer survivors who received adjuvant therapies outside MSKCC will be asked to self-report the type and duration of cancer treatments received. Exclusion Criteria: - Undergoing active cancer treatment (ongoing tamoxifen use, hormone replacement therapy or use of biologics are permitted) - Evidence of encephalopathy, psychotic illness or cognitive impairment severe enough to preclude giving informed consent to the study staff, or completing the survey instruments of the study. |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Memorial Sloan-Kettering Cancer Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Memorial Sloan Kettering Cancer Center | Beth Israel Medical Center, Vanderbilt University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Descriptive statistics will be generated to describe the prevalence of pain and its psychosocial correlates. | 1 to 10 years post-treatment completion | No |
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