Evaluation of the Effect of a Postural Reflex Rehabilitation Program on a Foam Surface on Stress Urinary Incontinence in Women

NCT ID: NCT04390204

Last Updated: 2025-09-24

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 116 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-09-21
• Study Completion Date: 2025-11-21

Brief Summary

Urinary incontinence is defined by the International Continence Society as "any involuntary loss of urine complained by the patient". UI is a debilating condition affecting 25% to 45% of the female population. It is a recognized factor impairing the women's quality of life in women. Age, type and severity of UI as well as stress, fears and beliefs are variables that significantly affect the quality of life scores . Its costs are estimated at 2% of the health budget in European countries. Stress urinary incontinence (SUI) is characterized by a loss of urine that occurs with increased intra-abdominal pressure, such as coughing, laughing, sneezing, jumping, running, lifting loads or any other physical activity

. SUI accounts for 50% of UI types. For HAS (Haute Autorité de Santé), the first-line treatment is a conservative, non-medicinal and non-surgical treatment. Hay Smith's 2010 literature review concludes that pelvic floor muscle rehabilitation (PMP) must be the first-line treatment for SUI. However, there is a lack of evidence to define the best treatment regimen for PFM rehabilitation.

For 25 years, we have been performing assessment and rehabilitation programs for urinary incontinence. We see daily, as literature suggests, a link between continence and postural control. Previous studies, such as that we carried out within our service, tend to confirm the positive impact of reflex postural control on continence. Our team has already shown the feasibility of such a program and its effectiveness on stress urinary incontinence. Foam surfaces are devices used in the rehabilitation of reflex postural control. Several studies have shown that rehabilitation programs on foam surfaces improve reflex postural control better than the same exercises on stable ground. Smith et al. have shown impaired motor control of MPP on foam surfaces in women with stress urinary incontinence. However, the effect of a rehabilitation program with foam surface on urinary symptoms has never been evaluated.

For our main outcome, we propose to follow the recommendations of L. Rimstad in his recent prospective study of SUI assessment in 147 subjects aged 36 to 63 years, wich seems more in accordance with postural control disorder than the "gold standard" supine cough test wich has been found to have low sensitivity. The test pad on a trampoline allows to object a SUI in 91% of the negative patients to the test pad on firm surface. It therefore makes it possible to object stress urinary incontinence without invasive urodynamic investigations. It therefore seems justified for the comfort of our patients and the relevance of our results. The preliminary assessments and the skills of the physiotherapist make it possible to assess the patient's ability to perform this test. Our experience of carrying out trampoline tests or exercises for 25 years, as of the Rimstad team in the context of the treatment of SUI for 10 years, allows us to carry out this test in good conditions of efficiency , comfort and safety. Thus, we hypothesize that a rehabilitation program by supervised reflex postural control exercises on a foam surface can reduce the volume of urinary leakage in women. This study will also show the influence of such a program on symptoms and quality of life in women with urinary incontinence.

Innovative nature of our study We do not find in the literature any evaluation of the effectiveness of exercises on foam surface on stress urinary incontinence Our protocol, by its minimally invasive nature, would promote a better emotional experience for our patients Most studies in the context of incontinence are based on a semi-objective outcome assessment with symptoms questionnaire. We suggest using the short stress pad test, a more objective test for women, recommended by several authors We will observe the impact of our protocol on pelvic and low back pain, quality of life and any restrictions on social participations We hope to confirm the best acceptance of non-invasive treatments, without intravaginal probe in continence rehabilitation

Our protocol goes in the direction of:

• Literature reviews on urinary incontinence through supervised group sessions
• WHO's recommendations on the maintenance of balance and physical functions, and also the prevention of falls in adults

Conditions

Urinary Incontinence,Stress

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Experimental

Motor control exercises are performed on foam mats. The physiotherapist instructs them, and gives a description on paper, as well as a USB key allowing to view the exercises on video. A supervised home self-rehabilitation program on foam mats is implemented.

Group Type: EXPERIMENTAL

intervenions

Intervention Type: OTHER

• Motor control exercises
• A supervised home self-rehabilitation program

control

According to the recommendations of learned societies, patients are offered voluntary MPP contraction work, in strength and endurance, in increasing complexity, under manual endocavitary control and under biofeedback. A supervised program of self-rehabilitation at home by voluntary contraction of MPP is set up.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

intervenions

• Motor control exercises
• A supervised home self-rehabilitation program

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 9≥18
• Patient with urinary incontinence according to the ICS criteria
• Patient affiliated to social security
• Patient having read and understood the information letter and signed the consent form
• Woman of childbearing age with effective contraception or menopausal status

Exclusion Criteria

• Neurological, psychiatric and digestive pathology wich induces stress urinary incontinence
• Pregnant or parturient or lactating woman
• Person deprived of liberty by administrative or judicial decision or a person placed under the safeguard of justice, or guardianship or curatorship
• Anti-cholinergic treatment initiated less than 3 months ago
• Patient unable to complete the 15 planned visits to physiotherapist
• Patient participating in another clinical trial
• Patient unable to perform the first stress test pad
• No urinary leakage noted during the stress pad test (difference of weight before and after protection pad test = 0 g)

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Rouen

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Cabinet Rééducation Grabels

Grabels, , France

Site Status: RECRUITING

cabinet de rééducation LINGOLSHEIM

Lingolsheim, , France

Site Status: RECRUITING

Cabinet Rééducation Poitiers

Poitiers, , France

Site Status: TERMINATED

CHU de ROUEN

Rouen, , France

Site Status: RECRUITING

cabinet SCM feeling

Saint-Étienne-du-Rouvray, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Déborah lebedieff

Role: CONTACT

deborah.lebedieff@chu-rouen.fr

0232888265 ext. +33

Facility Contacts

nolwenn quemener

Role: primary

aurélie lourenco

Role: primary

benoit steenstrup

Role: primary

benoit.stennstrup@chu-rouen.fr

benoit steenstrup

Role: primary

References

Hay-Smith EJC, Starzec-Proserpio M, Moller B, Aldabe D, Cacciari L, Pitangui ACR, Vesentini G, Woodley SJ, Dumoulin C, Frawley HC, Jorge CH, Morin M, Wallace SA, Weatherall M. Comparisons of approaches to pelvic floor muscle training for urinary incontinence in women. Cochrane Database Syst Rev. 2024 Dec 20;12(12):CD009508. doi: 10.1002/14651858.CD009508.pub2.

Reference Type: DERIVED

PMID: 39704322 (View on PubMed)

Other Identifiers

2017/389/HP

Identifier Type: -

Identifier Source: org_study_id