Electrostimulation PROTOCOL Incontinence

Not Applicable

Completed

• Conditions: Female Stress Incontinence

• Registration Number: NCT03682926
• Lead Sponsor: Hospital Universitário Professor Edgard Santos

Brief Summary

To verify the effect of an adapted electrostimulation (EE) protocol for stress and mixed urinary incontinence (SUI / M) and its impact on quality of life (QoL)

Detailed Description

Controlled and randomized clinical trial performed at the Physiotherapy Outpatient Clinic at the Magalhães Neto Pavilion of ComHUPES / UFBA. Women aged between 30 and 65 years and diagnosis of SUI / IUM. The patients were allocated to two groups (GA) submitted to selective electrostimulation for tonic fiber, phasic fibers IIa / IIb and different times of electrical stimulation; (GB) used 50hz for all fibers by 20mm, both answered the questionnaire King's Health Questionnaire (KHQ).

Study Timeline

• Study Start: 2014-10
• Primary Completion: 2014-11
• Study First Submitted: 2015-03-11
• Study Completion: 2015-12
• Study First Submitted QC: 2018-09-20
• Study First Posted: 2018-09-25
• Status Verified: 2018-10
• Last Update Submitted: 2018-10-01
• Last Update Posted: 2018-10-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

• women between the ages of 30 and 65
• With diagnosis of stress urinary incontinence and / or mixed
• Perineal muscle weakness
• Accepted to sign the TCLE

Exclusion Criteria

• Women with neurological changes
• Pregnant women
• IUD use
• Pacemaker
• Genitourinary tract infection
• Cancer
• Refuse to sign the TCLE

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
contractile function of the perineal musculature	3 months	Perineal muscle function evaluated subjectively by vaginal touch using the PERFECT system to measure strength (graded from 0 to 5), strength (holding capacity of contraction recorded in seconds) and number of contractions of tonic and phasic fibers (ability to repeat muscle contractions perineal). Objectively, the vaginal cones were used to determine which load the patient was able to support (kit with 5 cones with weights ranging from 20 to 70g)

Secondary Outcome Measures

Name	Time	Method
King's Health Questionnaire	3 months	It allows qualitative evaluation of the impact of urinary incontinence on the quality of life of women, it is responsible for 20 questions, divided into 8 domains, in addition to these domains, there are two other independent scales: the first evaluates the severity of UI (severity measures) and the second, the presence and intensity of urinary symptoms through the scale of urinary symptoms (VAS) where there is a graduation from 0 to 10, where the higher the score, the higher the severity