Evaluation of Programs of Reeducation for Urinary Incontinence in Woman

Not Applicable

Terminated

• Conditions: Urinary Incontinence
• Interventions: Other: Reference method; Other: CMP ® method

• Registration Number: NCT02899520
• Lead Sponsor: Hopital Foch

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)

Detailed Description

Not available

Study Timeline

• Study Start: 2014-11-10
• Study First Submitted: 2016-09-09
• Study First Submitted QC: 2016-09-09
• Study First Posted: 2016-09-14
• Primary Completion: 2019-10-18
• Study Completion: 2019-10-18
• Status Verified: 2019-12
• Last Update Submitted: 2019-12-31
• Last Update Posted: 2020-01-03

Recruitment & Eligibility

• Status: TERMINATED
• Sex: Female
• Target Recruitment: 60

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

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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.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group A	Reference method	Reference method
Group B	CMP ® method	CMP ® method (Knowledge and Control of Perineum)

Primary Outcome Measures

Name	Time	Method
USP (Urinary Symptoms Profile) score	38 weeks	Urinary Symptoms Profile score

Trial Locations

Locations (1)

Hopital Foch; 🇫🇷 Suresnes, France