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Life sciences · Interventional Study
ClinicalTrials.gov · October 1, 2026
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Interventional Study.
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Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT00932997). This is a study registration, not published results. Lead sponsor: City of Hope Medical Center. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 300 participants (ESTIMATED). Conditions: Breast Cancer, Cancer Survivor, Psychosocial Effects of Cancer and Its Treatment. Interventions: BEHAVIORAL: telephone-based intervention; OTHER: counseling intervention; OTHER: educational intervention; OTHER: questionnaire administration; PROCEDURE: psychosocial assessment and care; PROCEDURE: quality-of-life assessment. Primary outcome measures: Increased knowledge about the psychological and physical impact of breast cancer , 9 months post study enrollment; Improved psychological functioning (depression and anxiety) , 9 months post study enrollment; Improved family and social functioning (changes in family and partner communications) , 9 months post study enrollment. Brief summary: RATIONALE: Telephone sessions and survivorship booklets may increase knowledge about the psychological and physical impact of breast cancer and increase awareness of available resources. It is not yet known whether survivorship booklets are more effective when given alone or together with individual telephone sessions in informing breast cancer survivors. PURPOSE: This randomized clinical trial is studying individual telephone sessions given together with survivorship booklets compared with survivorship booklets alone to see how well they work in increasing knowledge about the impact of breast cancer in African American and Latina breast cancer survivors.