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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 6 February 2017
Main ID:  ACTRN12617000162314
Date of registration: 30/01/2017
Prospective Registration: Yes
Primary sponsor: Wroclaw Medical University
Public title: Electromyographic evaluation of the effect of pelvic floor muscle training to improve the function of the lower urinary tract in women with ischemic stroke
Scientific title: Electromyographic evaluation of the effect of pelvic floor muscle training to improve the function of the lower urinary tract in women with ischemic stroke: a prospective, randomized study with a control group.
Date of first enrolment: 20/02/2017
Target sample size: 40
Recruitment status: Not yet recruiting
URL:  http://www.anzctr.org.au/ACTRN12617000162314.aspx
Study type:  Interventional
Study design:  Randomised controlled trial 
Phase: 
Countries of recruitment
Contacts
Key inclusion & exclusion criteria
Health Condition(s) or Problem(s) studied
ischemic stroke
urinary incontinence
Intervention(s)
Participants will be randomly assigned to one of two comparison groups: A group - group, which will be used pelvic floor muscle training and B group (control) - a group without specialized training of the pelvic floor muscles. In group A will be applied the pelvic floor muscle training. Therapy will be held for ten days (two weeks at five sessions per week) and each will last about 30 minutes a day. The whole therapy will be carried out under the supervision of a therapist at the hospital. Participants will be recruited from among patients of the hospital Selection of exercises will be individual determined, in depends on the function of the lower urinary tract and the condition of the tested women (physiotherapist decision). Training will take into account the contractions of the pelvic floor muscles. Participants will perform contraction lasting a few seconds (depending on the condition of the patient, with a break lasts twice as long). They will also be carried out short, rapid contraction of this muscle. In this training, a electromyograph with the function of the visual biofeedback will be used. Feedback on muscle contraction provided via a screen for participants throughout each session via sEMG sensors. Each training session will be supervised and managed by a physiotherapist.
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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