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The Efficacy of Pre-operative Educational Pelvic Floor Intervention on Urinary Continence

Primary Purpose

Prostatectomy, Pelvic Floor Disorders

Status
Active
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Pre operative exercise
Control Group
Sponsored by
European Institute of Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostatectomy focused on measuring Prostatectomy, Pelvic Floor Disorders, Robotic Surgical Procedures, rehabilitation

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent form
  • Age >= 40 <= 70 years old
  • Body mass Index <= 27
  • Indication of robotic prostate surgery
  • Tumor with clinical stage T1 and T2.
  • Extracapsular Extension Score <= 3, measured with magnetic resonance before surgery.

Exclusion Criteria:

  • Pathologic T3 tumor with radiotherapy indication
  • Previous prostate surgery
  • Previous urinary incontinence.
  • Metabolic disorder
  • Central or peripheral neurologic disorders
  • Inability to understand informed consent or to carry out the rehabilitation protocol autonomously.

Sites / Locations

  • Istituto Europeo di Oncologia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pre operative exercise

Control group

Arm Description

The educational pelvic floor intervention group will receive one months before surgery a physiotherapy visit were will be explain to patients and care giver the pelvic floor anatomy and biomechanics and how perform the exercises to be follow at home focusing on pelvic muscles awareness and contraction. Patients and care giver will receive a daily exercise diary to fill at home and will be advised to follow the exercise program.

The control group will be just informed about the study protocol and will not receive any pre-operative intervention.

Outcomes

Primary Outcome Measures

Change in self-reported urinary continence
Continence (completely dry patient) will be defined as the sum of no urinary leakage reported by the patient in his bladder diary

Secondary Outcome Measures

The degree of urinary incontinence.
Assesment of the degree of urinary incontinence based on a 24 hours pad test.
Quality of life instrument
Assesment of quality of life using the The Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire.
Assesment of the post traumatic distress using the Impact of event Scale (IES).
Scale range from 0 to 4 with lower values representing better outcomes
Assesment of the individual resilience with the resilience scale for adults (RSA).
Scale range from 1 to 5 with lower values representing better outcomes
Assesment of the urinary status with the International Consultation on Incontinence (ICIQ) Questionnaire.
Summed of sub scales range from 0 to 3, 0 to 6 and 1 to 10. Minimum score of 1 and maximum score of 19, with lower values representing better outcomes

Full Information

First Posted
October 18, 2018
Last Updated
June 27, 2023
Sponsor
European Institute of Oncology
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1. Study Identification

Unique Protocol Identification Number
NCT03714984
Brief Title
The Efficacy of Pre-operative Educational Pelvic Floor Intervention on Urinary Continence
Official Title
The Efficacy of Pre-operative Educational Pelvic Floor Intervention on Urinary Continence in Patients Underwent Robotic Prostatectomy. A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 15, 2018 (Actual)
Primary Completion Date
December 4, 2019 (Actual)
Study Completion Date
December 4, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
European Institute of Oncology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Prostate cancer is the most common type of cancer between male population and urinary incontinence (UI) is the most common of long-term sequelae. Nowadays, robotic prostatectomy became the surgery standard but there is still discrepant results regards the incidence of UI and there is a lack of studies about the use of pelvic floor rehabilitation in this population. Our study aims to assesses the efficacy of preoperative educational method in urinary incontinence after robotic prostatectomy.
Detailed Description
Prostate cancer is the most common type of cancer between male population, with 161,300 new cases a year in the USA and an incidence of 10% in Italy. Since many years surgery is the treatment of choice, both at an early stage and in advanced cases, but involves side effects. From the post-operative problem presents in literature, urinary incontinence (UI) is the most common of long-term sequelae and significantly affects the quality of life and the psychological aspect in the post-surgical period. The incidence of UI after prostatectomy surgery varies between 0.8% and 87% in the first 3 and 6 months and between 5% and 44.5% after 1 year. This variability depends on the UI definition and the type of measurement used, which are not homogeneous among the various studies in the literature. Evaluations that are not objective make it difficult to compare the results obtained, thus creating discrepancies. To date, robotic prostatectomy is becoming the gold standard for its recognized greater accuracy when compared with the open surgery and laparoscopic procedure, with a reduced learning curve for operators and giving better post-surgical results. Progress technological aspects, such as the three-dimensional vision of the operative field, the macroscopic magnification and better image resolution, have made the robotic procedure a less invasive surgery with better functional outcomes. Despite these factors, UI is still present and in the majority of cases management is not completely evidence based. Moreover there is not yet a definite consensus regarding the predictive factors (age, disease stage, body weight, prostate volume and other comorbidities) in the incidence of the UI. When patients presents UI diagnoses, the conservative intervention through the pelvic floor rehabilitation is recommended in an attempt to reduce the impact of this complication. Muscle strengthening and pelvic floor awareness after surgery are used for years in clinical practice with results widely documented in the literature, but their effectiveness in the pre-operative period, especially if after robotic surgery, has not yet been sufficiently studied. Currently, there are discrepant results mainly due to the type of rehabilitative methodology applied and the time of beginning the preoperative treatment. Our study tries to evaluate, through an objective and reproducible measurement, the efficacy of a preoperative educational method in urinary incontinence after robotic prostatectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatectomy, Pelvic Floor Disorders
Keywords
Prostatectomy, Pelvic Floor Disorders, Robotic Surgical Procedures, rehabilitation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Superiority trial with 1:1 allocation ratio, randomized with two-arm parallel group
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pre operative exercise
Arm Type
Experimental
Arm Description
The educational pelvic floor intervention group will receive one months before surgery a physiotherapy visit were will be explain to patients and care giver the pelvic floor anatomy and biomechanics and how perform the exercises to be follow at home focusing on pelvic muscles awareness and contraction. Patients and care giver will receive a daily exercise diary to fill at home and will be advised to follow the exercise program.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
The control group will be just informed about the study protocol and will not receive any pre-operative intervention.
Intervention Type
Other
Intervention Name(s)
Pre operative exercise
Intervention Description
After randomization participants will be allocated in two groups. The educational pelvic floor intervention group will receive two months before surgery a physiotherapy visit were will be explain to patients and care giver the pelvic floor anatomy and biomechanics and how perform the exercises to be follow at home focusing on pelvic muscles awareness and contraction.
Intervention Type
Other
Intervention Name(s)
Control Group
Intervention Description
The control group will be just informed about the study protocol and will not receive any pre-operative intervention.
Primary Outcome Measure Information:
Title
Change in self-reported urinary continence
Description
Continence (completely dry patient) will be defined as the sum of no urinary leakage reported by the patient in his bladder diary
Time Frame
1,3,6 months and 1 year after surgery
Secondary Outcome Measure Information:
Title
The degree of urinary incontinence.
Description
Assesment of the degree of urinary incontinence based on a 24 hours pad test.
Time Frame
1,3,6 months and 1 year after surgery
Title
Quality of life instrument
Description
Assesment of quality of life using the The Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire.
Time Frame
1,3,6 months and 1 year after surgery
Title
Assesment of the post traumatic distress using the Impact of event Scale (IES).
Description
Scale range from 0 to 4 with lower values representing better outcomes
Time Frame
1,3,6 months and 1 year after surgery
Title
Assesment of the individual resilience with the resilience scale for adults (RSA).
Description
Scale range from 1 to 5 with lower values representing better outcomes
Time Frame
1,3,6 months and 1 year after surgery
Title
Assesment of the urinary status with the International Consultation on Incontinence (ICIQ) Questionnaire.
Description
Summed of sub scales range from 0 to 3, 0 to 6 and 1 to 10. Minimum score of 1 and maximum score of 19, with lower values representing better outcomes
Time Frame
1,3,6 months and 1 year after surgery

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent form Age >= 40 <= 70 years old Body mass Index <= 27 Indication of robotic prostate surgery Tumor with clinical stage T1 and T2. Extracapsular Extension Score <= 3, measured with magnetic resonance before surgery. Exclusion Criteria: Pathologic T3 tumor with radiotherapy indication Previous prostate surgery Previous urinary incontinence. Metabolic disorder Central or peripheral neurologic disorders Inability to understand informed consent or to carry out the rehabilitation protocol autonomously.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luiz Felipe Nevola Teixeira, PT
Organizational Affiliation
European Institute of Oncology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istituto Europeo di Oncologia
City
Milano
State/Province
Lombardia
ZIP/Postal Code
20141
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28732186
Citation
Fossati N, Di Trapani E, Gandaglia G, Dell'Oglio P, Umari P, Buffi NM, Guazzoni G, Mottrie A, Gaboardi F, Montorsi F, Briganti A, Suardi N. Assessing the Impact of Surgeon Experience on Urinary Continence Recovery After Robot-Assisted Radical Prostatectomy: Results of Four High-Volume Surgeons. J Endourol. 2017 Sep;31(9):872-877. doi: 10.1089/end.2017.0085. Epub 2017 Jul 21.
Results Reference
background
PubMed Identifier
20227168
Citation
Centemero A, Rigatti L, Giraudo D, Lazzeri M, Lughezzani G, Zugna D, Montorsi F, Rigatti P, Guazzoni G. Preoperative pelvic floor muscle exercise for early continence after radical prostatectomy: a randomised controlled study. Eur Urol. 2010 Jun;57(6):1039-43. doi: 10.1016/j.eururo.2010.02.028. Epub 2010 Mar 1.
Results Reference
background
PubMed Identifier
18384853
Citation
Moore KN, Valiquette L, Chetner MP, Byrniak S, Herbison GP. Return to continence after radical retropubic prostatectomy: a randomized trial of verbal and written instructions versus therapist-directed pelvic floor muscle therapy. Urology. 2008 Dec;72(6):1280-6. doi: 10.1016/j.urology.2007.12.034. Epub 2008 Apr 2.
Results Reference
background
PubMed Identifier
16406909
Citation
Burgio KL, Goode PS, Urban DA, Umlauf MG, Locher JL, Bueschen A, Redden DT. Preoperative biofeedback assisted behavioral training to decrease post-prostatectomy incontinence: a randomized, controlled trial. J Urol. 2006 Jan;175(1):196-201; discussion 201. doi: 10.1016/S0022-5347(05)00047-9.
Results Reference
background

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The Efficacy of Pre-operative Educational Pelvic Floor Intervention on Urinary Continence

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