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Trial registered on ANZCTR
Registration number
ACTRN12608000321347
Ethics application status
Approved
Date submitted
10/06/2008
Date registered
11/07/2008
Date last updated
3/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Evaluation of quality of life in women with overactive bladder treated with two different methods of Electro Stimulation
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Scientific title
Evaluation of quality of life in women with overactive bladder treated with Transvaginal Electro Stimulation or of the Posterior Tibial Nerve
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
overactive bladder
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Condition category
Condition code
Physical Medicine / Rehabilitation
3413
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0
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Physiotherapy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Posterior Tibial Nerve (frequency of the current 20 Hz, width of the pulse 200 µs, intensity according to patients tolerance, 30 minutes of electro stimulation). The treatment was carried out once a week, totalling twelve weeks.
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Intervention code [1]
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Rehabilitation
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Comparator / control treatment
Transvaginal electro stimulation (frequency of the current10 Hz, width of the pulse 700 µs, intensity according to patients tolerance, 20 minutes of electro stimulation). The treatment was carried out once a week, totalling twelve weeks.
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Control group
Active
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Outcomes
Primary outcome [1]
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Quality of life assessed by SF-36 a generic quality life questionnaire , and I-QOL. a specific questionnaire of quality of life related urinary incontinence
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Assessment method [1]
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Timepoint [1]
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baseline before 12 weeks of electro stimulation and at 12 weeks after electro stimulation
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Secondary outcome [1]
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Clinical complaint of urine loss was assessed by a voiding diary of 24 hours and Visual Analog Scale (VAS). To assess the satisfaction with treatment it was used subjective evaluation for clinical complaints and satisfaction with treatment, in which the patient reported to be cured, or better and satisfied with treatment (not requiring other therapy), or better although not satisfied with the treatment (seeking alternative therapy), or unchanged.
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Assessment method [1]
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Timepoint [1]
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baseline before 12 weeks of electro stimulation and at 12 weeks after electro stimulation
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Eligibility
Key inclusion criteria
urodynamic diagnosis of overactive bladder or mixed urinary incontinence, without drug therapy or drug therapy for more than 3 months
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Minimum age
18
Years
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Maximum age
79
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
pregnant and pospartum, level III vaginal prolapses, pelvic tumor, urinary or vaginal infection, cardiac dispositves, nerologic disorders, cogntive problems, interruption of the drugtherapy during the reserch
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
6/03/2006
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
42
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Brazil
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State/province [1]
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Sao Paulo
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Funding & Sponsors
Funding source category [1]
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Other
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Name [1]
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Maira Menezes Franco
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Address [1]
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Av. Governador Lucas Nogueira Garcez
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Country [1]
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Brazil
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Primary sponsor type
University
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Name
University of São Paulo
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Address
Av Bandeirantes 3900, Ribeirão Preto- SP CEP 14049-900
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Country
Brazil
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto
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Address [1]
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Av Bandeirantes 3900, Ribeirao Preto- SP CEP 14049-900
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Country [1]
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Brazil
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Comite de Etica em pesquisa do HCFMRP-USP
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Ethics committee address [1]
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Ethics committee country [1]
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Brazil
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Date submitted for ethics approval [1]
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Approval date [1]
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04/12/2006
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Ethics approval number [1]
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13247/2006
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Summary
Brief summary
The objective of this study was to compare the effects of the treatment with intravaginal electro stimulation and with posterior tibial nerve electro stimulation in the life quality and complaints of urinary loss in women with overactive bladder. Method: It was constituted a sample that included 42 patients with overactive bladder or mixed urinary incontinence for treatment either by intravaginal electro stimulation or by the posterior tibial nerve electro stimulation. To assess the quality of life (QOL) questionnaire was used a generic quality life, the SF-36, and a questionnaire of quality specific to IU, the I-QOL. The reports of urinary loss and incommodious caused by the same respectively were evaluated by the voiding of 24 hours daily, and Visual Analog Scale (VAS). The treatment was carried out once a week, totalling twelve weeks. Result: The group that received posterior tibial nerve electro stimulation had significant improvement in three domains of the I-QOL, in VAS (p = 0.03), and four aspects of the miccional diary. For the group of intravaginal electro stimulation there was significant improvement in two domains of the SF-36, three domains of the I-QOL, in VAS (p <0.01) and four aspects of the miccional diary. The comparison of the two groups, after treatment didn’t reveal significant difference in any of the variables. Conclusion: There was improvements of the life quality by the use of the two treatment types, as well as a decrease of the complaints of urinary loss, however the group that received intravaginal electro stimulation obtained improvement in the scores in two domains of the generic questionnaire of life quality after the treatment, what didn't happen with the other group treatment.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Maíra menezes franco
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Address
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Av. Governador Lucas Nogueira Garcez n. 70. Ribeirão Preto -SP CEP 14051510
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Country
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Brazil
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Phone
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16 32346943
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Maíra menezes franco
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Address
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Av. Governador Lucas Nogueira Garcez n. 70. Ribeirão Preto -SP CEP 14051510
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Country
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Brazil
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Phone
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16 3632346943
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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