Prostate Cancer Clinical Trial

Physical Therapy for Men Undergoing Prostatectomy

Summary

The purpose of this study is to determine if pelvic floor muscle training with a physical therapist before and after surgery will improve health-related quality of life following robot-assisted radical prostatectomy.

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Full Description

Goals of the present study will be to determine whether initiating pelvic floor muscle training preoperatively improves quality of life symptoms related specifically to urinary health following robot-assisted radical prostatectomy. Drawing definitive conclusions from past studies is challenging secondary to various inconsistencies including: variability of physical therapy intervention, poorly defined definitions of continence, as well as poorly defined quality of life measurements. Additionally, the vast majority of studies combined open and robotic prostatectomy increasing cohort heterogeneity and further blurring interpretation of results. The investigators' study will focus exclusively on patients undergoing robot-assisted radical prostatectomy. Standardized pelvic floor muscle therapy as well as clearly defined patient outcomes (ie: validated questionnaires) will be utilized to determine whether preoperative initiation of formal pelvic floor physical therapy can improve health-related quality of life following surgery.

In the era of robot-assisted radical prostatectomy does physical therapist initiated preoperative pelvic floor muscle training lessen the expected postoperative drop off in urinary related quality of life and/or improve patient's recovery of continence following surgery?

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Eligibility Criteria

Inclusion Criteria:

Patients scheduling to undergo robot-assisted radical prostatectomy
Patients willing and able to complete the EPIC questionnaire in its entirety
Ability to provide informed consent

Exclusion Criteria:

Previous prostate surgery
Radiation treatment
History of incontinence defined as any pad use for urinary leakage in the past 6 months

Study is for people with:

Prostate Cancer

Estimated Enrollment:

160

Study ID:

NCT02558946

Recruitment Status:

Unknown status

Sponsor:

Indiana University

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There is 1 Location for this study

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IU Health Methodist Hospital and IU Health University Hospital
Indianapolis Indiana, 46202, United States More Info
Kim Smoot
Contact
317-962-0869
Ronald Boris, MD
Principal Investigator

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Study is for people with:

Prostate Cancer

Estimated Enrollment:

160

Study ID:

NCT02558946

Recruitment Status:

Unknown status

Sponsor:


Indiana University

How clear is this clinincal trial information?

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