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Evaluation of Programs of Reeducation for Urinary Incontinence in Woman

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02899520
Acronym
ReedPerinee
Enrollment
60
Registered
2016-09-14
Start date
2014-11-10
Completion date
2019-10-18
Last updated
2020-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Incontinence

Brief summary

The objective of this study is to compare two methods of pelvic floor muscle training: reference method versus CMP ® method ( (Connaissance et Maîtrise de Périnée : Knowledge and Control of Perineum)

Interventions

OTHERReference method

Electrostimulation associated to perineal training

OTHERCMP ® method

Method based on Knowledge and Control of Perineum

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients more than 18 years old and less than 75 years * Patients presenting an urinary incontinence of effort or mixed symptomatic associated with a pelvic statics disorder * Patients with a perineale reeducation prescription * Patients affiliated to a national insurance scheme or benefiting from such a program * Patients having given her written consent form

Exclusion criteria

* Nulliparous woman * Patients already operated for their incontinence * Patients with a prolapse of higher level at the stage II of the classification POP-Q (Pelvic Organ Prolapse Quantification) * Pregnant women * Patients presenting an associated anal incontinence, * Patients presenting a cancellation (section of marrow, syringomyelia for example) or an inversion of perineum control * Patients having given birth less than 6 months before the care * Patients having benefited from a pelvi-périnéale reeducation in the previous 12 months, * Patients presenting psychiatric disease * Patients presenting a vaginismus, * Patients presenting a contraindication to the practice of the electrostimulation.

Design outcomes

Primary

MeasureTime frameDescription
USP (Urinary Symptoms Profile) score38 weeksUrinary Symptoms Profile score

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026