Advanced Pelvic Floor Training Program for Prostate Cancer Surgery
AFPX
A Randomized Pilot Study of Conventional Versus Advanced Pelvic Floor Exercises to Treat Urinary Incontinence After Radical Prostatectomy
1 other identifier
interventional
88
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Jan 2015
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 3, 2014
CompletedFirst Posted
Study publicly available on registry
September 8, 2014
CompletedStudy Start
First participant enrolled
January 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 28, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
September 28, 2017
CompletedOctober 26, 2017
October 1, 2017
2.7 years
September 3, 2014
October 24, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Recruitment
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.
When recruitment is complete (approximately 12 months after study initiation; October 2015)
Adherence to intervention group
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.
26 weeks post-operatively
Study retention
Retention will be assessed by measuring attrition throughout the intervention period and at each assessment.
26 weeks post-operative
24-hour Pad Test for Urinary Leakage
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.
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operatively
Pelvic Floor Strength
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.
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26, weeks post-operatively
Secondary Outcomes (5)
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 Arms (2)
Usual Care
NO INTERVENTIONThe usual care group will receive generic pelvic floor muscle exercise (PMFX) instructions and demonstrations by the research coordinator at the initial post-operative time point. This will include instruction on how to engage the pelvic floor and specific PFMX prescription. Repetition volume will start at 20 repetitions per day during weeks 1-2; 60/day during weeks 3-4; and 90/day during weeks 5-6, and 100+/day for weeks 7-26. The total number of repetitions will be divided equally between rhythmic (contract and relaxed over one second) and sustained contractions (contract and hold for up to 10 seconds).
Advanced Pelvic Floor Exercise (APFX)
EXPERIMENTALParticipants in this group will receive detailed week-by-week description of the program. The program progresses participants through stages of training every two weeks, starting the introduction of basic PFMX, and slowly incorporates Pfilates and Hypopressives exercises until week 8, where patients will maintain the final stage of training until week 26 or urinary incontinence is completely resolved.
Interventions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Guelph-Humberlead
- Princess Margaret Hospital, Canadacollaborator
- University Health Network, Torontocollaborator
Study Sites (1)
University Health Network
Toronto, Ontario, M5G 2C4, Canada
Related Publications (1)
Santa Mina D, Au D, Alibhai SM, Jamnicky L, Faghani N, Hilton WJ, Stefanyk LE, Ritvo P, Jones J, Elterman D, Fleshner NE, Finelli A, Singal RK, Trachtenberg J, Matthew AG. A pilot randomized trial of conventional versus advanced pelvic floor exercises to treat urinary incontinence after radical prostatectomy: a study protocol. BMC Urol. 2015 Sep 16;15:94. doi: 10.1186/s12894-015-0088-4.
PMID: 26377550DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Scientist
Study Record Dates
First Submitted
September 3, 2014
First Posted
September 8, 2014
Study Start
January 1, 2015
Primary Completion
September 28, 2017
Study Completion
September 28, 2017
Last Updated
October 26, 2017
Record last verified: 2017-10