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Advanced Pelvic Floor Training Program for Prostate Cancer Surgery (AFPX)

Primary Purpose

Prostate Cancer Patients Undergoing Radical Prostatectomy

Status
Completed
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Advanced Pelvic Floor Muscle Exercise (APFX)
Sponsored by
University of Guelph-Humber
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer Patients Undergoing Radical Prostatectomy focused on measuring Prostate cancer, Radical prostatectomy, Pelvic floor muscle exercises, Pfilates, Hypopressives, Urinary Incontinence

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Usual Care

Advanced Pelvic Floor Exercise (APFX)

Arm Description

The 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).

Participants 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.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Quality of Life
Prostate specific quality of life will be measured using the Functional Assessment of Cancer Treatment-Prostate (FACT-P) and the Patient-Oriented Prostate Utility Scale (PORPUS).
3-Day Bladder Diary for Urinary Incontinence
The bladder diary is a standard instrument for self-reporting voiding patterns. Items include fluid intake, frequency of toilet voids, episode of urine loss, number of pads used, and activity during event for the three-day period. Bladder diaries are widely used in clinical trials assessing urinary incontinence after radical prostatectomy.
Self-Reported Urinary Incontinence, Prostate Symptoms, and Erectile Function
Urological symptoms are assessed using the International Prostate Symptom Score (IPSS). Additional, a single item regarding leaking urine and bladder control from the PORPUS will be used to evaluate incontinence. Erectile function will be assessed using the 5-item International Index of Erectile Function scale (5-IIEF).
Body Composition
Body composition will be assessed via bioelectrical impedance analysis, height, weight, waist and hip circumference, and body mass index.
Physical Activity
Physical activity level will be measured wight he 3-item Godin Leisure Time Exercise Questionnaire - Leisure Score Index (GLTEQ-LSI).

Full Information

First Posted
September 3, 2014
Last Updated
October 24, 2017
Sponsor
University of Guelph-Humber
Collaborators
Princess Margaret Hospital, Canada, University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT02233608
Brief Title
Advanced Pelvic Floor Training Program for Prostate Cancer Surgery
Acronym
AFPX
Official Title
A Randomized Pilot Study of Conventional Versus Advanced Pelvic Floor Exercises to Treat Urinary Incontinence After Radical Prostatectomy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
September 28, 2017 (Actual)
Study Completion Date
September 28, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guelph-Humber
Collaborators
Princess Margaret Hospital, Canada, University Health Network, Toronto

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer Patients Undergoing Radical Prostatectomy
Keywords
Prostate cancer, Radical prostatectomy, Pelvic floor muscle exercises, Pfilates, Hypopressives, Urinary Incontinence

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
88 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
The 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).
Arm Title
Advanced Pelvic Floor Exercise (APFX)
Arm Type
Experimental
Arm Description
Participants 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.
Intervention Type
Behavioral
Intervention Name(s)
Advanced Pelvic Floor Muscle Exercise (APFX)
Primary Outcome Measure Information:
Title
Recruitment
Description
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.
Time Frame
When recruitment is complete (approximately 12 months after study initiation; October 2015)
Title
Adherence to intervention group
Description
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.
Time Frame
26 weeks post-operatively
Title
Study retention
Description
Retention will be assessed by measuring attrition throughout the intervention period and at each assessment.
Time Frame
26 weeks post-operative
Title
24-hour Pad Test for Urinary Leakage
Description
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.
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operatively
Title
Pelvic Floor Strength
Description
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.
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26, weeks post-operatively
Secondary Outcome Measure Information:
Title
Quality of Life
Description
Prostate specific quality of life will be measured using the Functional Assessment of Cancer Treatment-Prostate (FACT-P) and the Patient-Oriented Prostate Utility Scale (PORPUS).
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operative
Title
3-Day Bladder Diary for Urinary Incontinence
Description
The bladder diary is a standard instrument for self-reporting voiding patterns. Items include fluid intake, frequency of toilet voids, episode of urine loss, number of pads used, and activity during event for the three-day period. Bladder diaries are widely used in clinical trials assessing urinary incontinence after radical prostatectomy.
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively
Title
Self-Reported Urinary Incontinence, Prostate Symptoms, and Erectile Function
Description
Urological symptoms are assessed using the International Prostate Symptom Score (IPSS). Additional, a single item regarding leaking urine and bladder control from the PORPUS will be used to evaluate incontinence. Erectile function will be assessed using the 5-item International Index of Erectile Function scale (5-IIEF).
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively
Title
Body Composition
Description
Body composition will be assessed via bioelectrical impedance analysis, height, weight, waist and hip circumference, and body mass index.
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 week post-operatively
Title
Physical Activity
Description
Physical activity level will be measured wight he 3-item Godin Leisure Time Exercise Questionnaire - Leisure Score Index (GLTEQ-LSI).
Time Frame
At baseline, approximately 1 week prior to surgery, and 2, 6, 12, 26 weeks post-operatively

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
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
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
26377550
Citation
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.
Results Reference
derived

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Advanced Pelvic Floor Training Program for Prostate Cancer Surgery

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