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Completed NCT00712751

The Sexual Health of Rectal Cancer Patients

Conditions: Rectal Cancer, Rectum

Sex: All
Ages: 21 Years – N/A
Healthy volunteers: No
Enrollment: 149
Sponsor: Memorial Sloan Kettering Cancer Center

Location: Mount Sinai Hospital New York New York

Summary

We know that treatment for rectal, colorectal or anal cancer can impact sexual function. This study aims to learn: * How the treatment affects emotional and social well-being. * How a new sexual health educational program affects you. Cancer patients seek education for lots of reasons. It often helps them cope because they can express their feelings with a trained professional. This study is open to individuals who have been treated for rectal, colorectal or anal cancer. It involves a new type of sexual health counseling program. It will teach participants skills that they can use to improve their sex lives. These skills may also improve physical and emotional well-being. We will compare the new type of sexual health program with the standard care patients receive after treatment for rectal, colorectal or anal cancer.

Eligibility Criteria

Inclusion Criteria: * At least six months post radiation and/or surgery for stage I-III rectal adenocarcinoma or rectosigmoid for cancer with an anastomosis at 15 cm or below and completed treatment * At least six months post radiation and/or chemotherapy for anal cancer. * Have no evidence of disease or recurrence * For women indicate Indicate moderate satisfaction or below on their overall sexual life (a score of "4" or lower on the question "Over the past 4 weeks, how satisfied have you been with your overall sexual life?" * For men indicate, and a score of "3" or lower on the question "How would you rate your confidence that you could get and keep an erection" for men) and a score of "2" or higher on the question "How much does this problem bother you? * In the judgment of the consenting professional interventionists, able to communicate in English well enough to work with English speaking and complete the study assessments. * Age 21 years or older. Exclusion Criteria: * Significant cognitive or psychiatric disturbance sufficient, in the investigator's judgment, to preclude participation in a psychotherapeutic intervention. * Are actively participating in protocol 06-151 * Participated in focus group or qualitative interview.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT00712751). StuddyBuddy aggregates publicly available trial information.