Postural Training for Standing and Sitting in Men Suffering From Post-prostatectomy Urinary Incontinence (EDULAPRO)
Existing research highlights the difficulty of identifying an optimal rehabilitation technique for improving male urinary continence. However, several authors have demonstrated the benefits of treatment based on improving movement control, often referred to as postural motor contro. The main principles are: respect for the neutral lumbopelvic position, reduction of intra-abdominal constraints and ecology of movement. With the aim of encouraging patient-centred clinical practice, patients are asked to fill in an assessment form on which they note the most disabling gestures with regard to their UI during the initial assessment. In our experience, 'sitting down or getting up from a chair' is the item most frequently and most severely reported. In practical terms, posture and body movements play a vital role in the management of pelvic strain. For example, excessive pressure on the bladder due to poor postural control would increase stress on the bladder. Optimal postural control would have the advantage of reducing and promoting continence mechanisms. If we take the example of the transition from sitting to standing, postural control aims to improve neuromuscular coordination and promote continence.
In the context of health education during the first session, it might be interesting to study the impact of modifying postural control when standing/sitting on urinary incontinence and how patients feel about it.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: benoit steenstrup, MKDE
- Phone Number: 02 32 88 82 65
- Email: benoit.steenstrup@chu-rouen.fr
Study Contact Backup
- Name: déborah lebedieff
- Phone Number: 0232888265
- Email: deborah.lebedieff@chu-rouen.fr
Study Locations
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Rouen, France
- CHU Rouen
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Contact:
- benoit steenstrup
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Vannes, France
- CH Bretagne Atlantique
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Men over the age of majority.
- Men who had had a prostatectomy within one year of inclusion.
- Positive response to the question 'Do you leak urine when you stand or sit up?
- Patients with a medical prescription for post-prostatectomy urinary incontinence rehabilitation.
- Patients who are able to understand and follow the instructions relating to postural education when standing up or sitting down.
- Patients who have read and understood the information note and who have not objected to participating in the research.
- Patients affiliated to a social security scheme.
Exclusion Criteria:
- Urinary leakage before prostatectomy (diagnosed by a doctor)
- Pad test ≤ 0 grams at the inclusion visit, before showing the postural control technique.
- On anticholinergic treatment initiated less than 3 months ago.
- Impossible to carry out postural control education (spinal surgery, serious neurological or orthopaedic pathology).
- Patients deprived of their liberty by an administrative or judicial decision or protected adults (under guardianship or trusteeship).
- Participation in other interventions: Individuals participating at the same time in other post-prostatectomy rehabilitation programmes or similar clinical studies.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
the sign of the difference between the results of the two pad tests of 3 times 24 hours.
Time Frame: 15 days
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15 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024/0203/OB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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