Skip to main content
Clinical Trials/NCT02233608
NCT02233608
Completed
Phase 1

A Randomized Pilot Study of Conventional Versus Advanced Pelvic Floor Exercises to Treat Urinary Incontinence After Radical Prostatectomy

University of Guelph-Humber1 site in 1 country88 target enrollmentJanuary 2015

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Prostate Cancer Patients Undergoing Radical Prostatectomy
Sponsor
University of Guelph-Humber
Enrollment
88
Locations
1
Primary Endpoint
Recruitment
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Radical prostatectomy is a common and effective treatment for prostate cancer but is associated with urinary incontinence that can persist for several months after surgery and significantly reduce quality of life. Studies have shown that routine performance of pelvic floor exercises after radical prostatectomy can aid in the recovery of urinary control; however, conventional pelvic floor exercises do not produce consistent results. Research indicates that incorporating other deep abdominal muscles can further activate the pelvic floor making it stronger than by activating the pelvic floor alone. Specifically, 'Pfilates' and 'Hypopressives' are two new techniques that combine traditional pelvic floor exercises with activation of supportive muscles. Our proposed study will be the first to test the effect of an advanced pelvic floor exercise training program that includes Pfilates and Hypopressives to treat urinary incontinence following radical prostatectomy. Our primary aim of this study is to assess the feasibility of conducting a full-scale RCT of an advanced pelvic floor exercise training program, including standard pelvic floor exercises, Pfilates, and Hypopressives techniques on urinary incontinence. Feasibility will be determined by measuring recruitment success, retention, outcome capture, and intervention adherence, tolerance, and safety. We hypothesize men under going radical prostatectomy for prostate cancer in the advance pelvic floor training program will report greater improvement in urinary incontinence and health-related quality of life.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
September 28, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Daniel Santa Mina

Scientist

University Health Network, Toronto

Eligibility Criteria

Inclusion Criteria

  • Men with localized prostate cancer (stage cT1-cT2) who have consented for radical prostatectomy (open retropubic, laparoscopic, robot-assisted laparoscopic)
  • Between the the ages of 40 and 80 years
  • Proficient in English

Exclusion Criteria

  • i) Diagnosed with a known neurological disease, autoimmune connective tissue disorder;
  • ii) Have prior experience with pelvic floor training by a healthcare provider;
  • iii) Have uncontrolled hypertension;
  • iv) Have diagnosed COPD (Chronic Obstructive Pulmonary Disease) and/or chronic restrictive respiratory disease; or
  • v) Have a history of inguinal herniation

Outcomes

Primary Outcomes

Recruitment

Time Frame: When recruitment is complete (approximately 12 months after study initiation; October 2015)

Prior pelvic floor training trials in prostate cancer patients undergoing radical prostatectomy have observed recruitment rates of 21-70%. We will measure recruitment success through participant recruitment per week and record reasons for non-participation from those who inquire about the study and are eligible to participate but refuse.

Adherence to intervention group

Time Frame: 26 weeks post-operatively

Adherence to the two groups (standard pelvic floor exercises and advanced pelvic floor exercises) will be measured through a logbook that is included in their respective program manuals as well as a logbook completed by the research coordinator during the weekly telephone communications.

Study retention

Time Frame: 26 weeks post-operative

Retention will be assessed by measuring attrition throughout the intervention period and at each assessment.

24-hour Pad Test for Urinary Leakage

Time Frame: At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operatively

A 24-hour pad test will be used to measure urinary incontinence by assessing the quantity of urine lost in one day. A urinary leakage pad is measured after a 24-hour period and compared to the unused pad weight and is used to most accurately assess the severity of urinary incontinence.

Pelvic Floor Strength

Time Frame: At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26, weeks post-operatively

Digital rectal examination of pelvic floor strength by a specially trained pelvic floor physiotherapist will be conducted. Pelvic floor strength will be graded on the Modified Oxford Scale.

Secondary Outcomes

  • Quality of Life(At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operative)
  • 3-Day Bladder Diary for Urinary Incontinence(At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively)
  • Self-Reported Urinary Incontinence, Prostate Symptoms, and Erectile Function(At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively)
  • Body Composition(At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively)
  • Physical Activity(At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operatively)

Study Sites (1)

Loading locations...

Similar Trials