Condition
Advanced Malignant Mesothelioma|Carcinoma of the Appendix|Ovarian Sarcoma|Ovarian Stromal Cancer|Pseudomyxoma Peritonei|Recurrent Colon Cancer|Recurrent Malignant Mesothelioma|Recurrent Ovarian Epithelial Cancer|Recurrent Ovarian Germ Cell Tumor|Stage III Colon Cancer|Stage III Ovarian Epithelial Cancer|Stage III Ovarian Germ Cell Tumor|Stage IV Colon Cancer|Stage IV Ovarian Epithelial Cancer|Stage IV Ovarian Germ Cell Tumor|Unspecified Childhood Solid Tumor, Protocol Specific
Estimated Enrollment: 10
Age Group: Child, Adult, Senior
Gender: All
Study Type: Interventional
Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Supportive Care
Study ID Numbers: CCCWFU 97110|NCI-2010-00980
Study First Received: May 13, 2010
Last Updated: January 17, 2017
Estimated Primary Completion Date: April 2011
Primary Outcome Measures:
Assess feasibility of instituting an orientation program, brief follow up care and phone calls in this patient population|Reduce pre-treatment distress and anxiety|Improve pre-treatment self-efficacy|Provide educational material delivered by the SRB|Improve overall post-operative QOL ratings at 3 months, relative to discharge
Sponsors and Collaborators:
Wake Forest University Health Sciences
Website Link: https://ClinicalTrials.gov/show/NCT01126346
