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Clinical Trial: Quality of Life in African-American or Caucasian Women Survivors of Breast Cancer
This study is not yet open for patient recruitment.
Verified by National Cancer Institute (NCI) December 2005
Purpose
RATIONALE: Studying quality of life in cancer survivors may help determine the long-term effects of breast cancer and may help improve the quality of life for future cancer survivors.
PURPOSE: This clinical trial is studying the quality of life in African-American or Caucasian women survivors of breast cancer.
| Condition | Intervention |
|---|---|
| Cancer Depression Fatigue Quality of Life Sexual Dysfunction and Infertility Sleep Disorders Spiritual Concerns | Procedure: complications of therapy assessment/management Procedure: fatigue assessment/management Procedure: psychosocial assessment/care Procedure: quality-of-life assessment Procedure: screening intervention Procedure: study of socioeconomic and demographic variables Procedure: supportive care/therapy |
MedlinePlus related topics: Cancer; Cancer Alternative Therapies; Depression; Sleep Disorders
Genetics Home Reference related topics: Cancer; Cancer--Living with Cancer
Study Type: Interventional
Study Design: Treatment
Official Title: Survey Study of Long-Term Disease-Specific, Generic, and Global Quality of Life in African-American or Caucasian Women Breast Cancer Survivors
OBJECTIVES:
- Compare African-American survivors of breast cancer to Caucasian survivors of breast cancer on disease-specific, generic, and global quality of life measures.
- Compare African-American survivors of breast cancer to an age-matched control group of African-American women with no history of breast cancer on these quality of life measures.
OUTLINE: Patients and healthy participants complete a battery of quality of life (QOL) questionnaires over approximately 65 minutes by mail or over the phone, including the Sexual Function Index, Functional Assessment of Cancer Therapy - Fatigue, Concerns About Recurrence Scale, and other measures of symptoms/side effects, the RAND Physical Functioning -10 Scale, Center for Epidemiologic Studies - Depression Scale, assessment of family function/social support, ENRICH Marital Satisfaction Scale, Reed Spiritual Perspective Scale, assessment of coping, and the Index of Well-being. Demographic, disease, treatment, and comorbidity information is collected using questionnaires and medical chart review.
PROJECTED ACCRUAL: A total of 195 patients and healthy participants will be accrued for this study.
Eligibility
DISEASE CHARACTERISTICS:
- Meets 1 of the following criteria:
- African-American or Caucasian breast cancer survivor
- Diagnosed with stage I-III breast cancer between the years of 1995-2003
- Receiving follow up care at the Indiana University Cancer Center (IUCC), the IUCC Northside Clinic, Spring Mill Clinic, or Wishard Memorial Hospital
- Healthy African-American
- Acquaintance of an African-American breast cancer survivor whose age is within five years of that of the patient
- Not known to have breast cancer
PATIENT CHARACTERISTICS:
- Female
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
Location and Contact Information
Kathleen Russell, RN, DNS, Study Chair, Indiana University School of Medicine
More Information
Clinical trial summary from the National Cancer Institute''''s PDQ® database
Last Updated: December 21, 2005
Record first received: December 20, 2005
ClinicalTrials.gov Identifier: NCT00268502
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2006-01-10

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