Quality of Life in Patients Undergoing Total Pelvic Exenteration

This protocol represents the first study to comprehensively evaluate QOL in a mixed population of male and female patients treated with total, anterior or posterior pelvic exenteration. This unique approach to QOL assessment which is both domain-centered and able to emphasize individual differences through the C-SHIP model has the potential to set the standard for evaluating QOL in patients who undergo extensive pelvic surgery. The longitudinal design of this study facilitates the documentation of patients'responsiveness to change. By analyzing participants' responses at intervals we will be able to document the redefinition of life goals which occurs as patients adapt to their new health status. The data and analysis completed in first three years of this study will be used to generate further hypotheses for future investigation.

Inclusion criteria

• All patients (male and female) who are scheduled to undergo total, anterior or posterior pelvic exenteration for pelvic malignancies arising in gynecologic, colorectal or urologic organs are eligible for participation in the study. Anterior or posterior pelvic exenteration must involve formation of a permanent ostomy (urostomy or colostomy).
• Participants must be able to speak and read English proficiently.
• Participants must be able to provide written informed consent.
• Patients must be 18 years of age or older to enroll.

Exclusion criteria

• Subjects may be excluded or withdrawn from the study based on the following criteria.
• Development of a cognitive or psychiatric deficit resulting in an inability to provide meaningful informed consent
• Inability to speak or read in English.