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Trial registered on ANZCTR
Registration number
ACTRN12617000938303
Ethics application status
Approved
Date submitted
14/06/2017
Date registered
28/06/2017
Date last updated
11/02/2021
Date data sharing statement initially provided
11/06/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
A cohort study of the effects of transcutaneous electrical nerve stimulation (TENS) on psychosocial and incontinence outcomes in children with overactive bladder syndrome
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Scientific title
A cohort study of the effects of transcutaneous electrical nerve stimulation (TENS) on psychosocial and incontinence outcomes in children with overactive bladder syndrome
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Secondary ID [1]
292184
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None
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Universal Trial Number (UTN)
Not applicable
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Trial acronym
Not applicable
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Linked study record
.
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Health condition
Health condition(s) or problem(s) studied:
Overactive bladder syndrome in children
303656
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Condition category
Condition code
Renal and Urogenital
303042
303042
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0
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Other renal and urogenital disorders
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Mental Health
303043
303043
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0
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Other mental health disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
TENS is based on the gate control theory of abolishing the local micturition reflex arc. The sticky electrodes are applied on the lower back, on the bladder dermatome S2, S3 and S4. The child is encouraged to wear the TENS for 1 hour every day for three months. The TENS is set at a frequency 10 Hz with the current density set as has as tolerated by the child. Children attending the urinary incontinence clinics at The Children's Hospital at Westmead and John Hunter Children’s Hospital in Newcastle, who are diagnosed with overactive bladder who require additional treatment for their overactive bladder after at least one month of urotherapy will be invited to participate in the study. Children are referred by their general practitioners or specialists to the clinics. Parents will be informed that parasacral TENS is an alternative to the pharmacological treatment with anticholinergics. Those wishing to participate in the study and have provided informed consent will be provided with a TENS machine for three months.
Children and their parents will be instructed on how to use the TENS, which will be used in their homes at times convenient to them. the child will be asked to wear the TENS (set at 10 Hz) for 60 minutes per day for 3 months. The study coordinator will contact study participants every 4 weeks to provide additional support and to evaluate their progress. Participants will be asked to complete 3 baseline questionnaires at enrolment and after 3 months of TENS use.
As this study forms part of an international collaboration, data from the Australian sites will be also be compared with data from Germany and Brazil.
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Intervention code [1]
298338
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Treatment: Devices
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Comparator / control treatment
No Control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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quality of life (pinQ score)
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Assessment method [1]
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Timepoint [1]
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pre and post treatment
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Primary outcome [2]
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behaviour (SDQ score)
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Assessment method [2]
302490
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Timepoint [2]
302490
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pre and post treatment
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Secondary outcome [1]
335908
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Change in ICIQ-CLUTS score
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Assessment method [1]
335908
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Timepoint [1]
335908
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pre and post treatment
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Secondary outcome [2]
336175
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Change in mean voiding frequency
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Assessment method [2]
336175
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Timepoint [2]
336175
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by comparing 48-h bladder diary data pre and post treatment
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Secondary outcome [3]
336176
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Change in maximum voided volume
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Assessment method [3]
336176
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Timepoint [3]
336176
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by comparing 48-h bladder diary pre and post treatment
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Secondary outcome [4]
336178
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Change in post void residual urine
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Assessment method [4]
336178
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Timepoint [4]
336178
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by comparing bladder scan pre and post treatment
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Eligibility
Key inclusion criteria
All children who present to the outpatient incontinence clinics at the Children’s Hospital at Westmead and John Hunter Children’s Hospital with overactive bladder who have had at least one month of urotherapy, for which treatment with TENS is indicated, where parents chose to use TENS instead of anticholinergic medications as first line therapy
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Minimum age
4
Years
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Maximum age
17
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Children who have previously used or are currently using anticholinergics for overactive bladder syndrome. Also patients with concomitant faecal incontinence.
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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)
not applicable
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
not applicable
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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
Single group
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Other design features
Before after study - comparison with baseline
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Sample size 30 at both CHW and JHCH: A sample of 30 patients will have 80% power at 5% one-sided significance to detect a within-patient improvement of 0.5 standard deviations in the continuous outcomes SDQ and PinQ scores after 3 months of treatment with TENS using a one-sample t-test.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/09/2017
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Actual
16/03/2018
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Date of last participant enrolment
Anticipated
31/12/2019
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Actual
11/03/2020
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Date of last data collection
Anticipated
30/03/2020
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Actual
14/07/2020
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Sample size
Target
30
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Accrual to date
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Final
31
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
8338
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The Children's Hospital at Westmead - Westmead
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Recruitment hospital [2]
8339
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John Hunter Children's Hospital - New Lambton
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Recruitment postcode(s) [1]
16408
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2145 - Westmead
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Recruitment postcode(s) [2]
16409
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2305 - New Lambton
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Funding & Sponsors
Funding source category [1]
296721
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Hospital
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Name [1]
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The Children's Hospital at Westmead
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Address [1]
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Hawkesbury Rd Westmead NSW 2145
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Country [1]
296721
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Australia
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Primary sponsor type
Individual
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Name
Assoc Prof Patrina Caldwell
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Address
The Children's Hospital at Westmead
Locked Bag 4001
Westmead NSW 2145
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Country
Australia
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Secondary sponsor category [1]
295688
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None
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Name [1]
295688
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Address [1]
295688
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Country [1]
295688
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Other collaborator category [1]
279601
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Individual
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Name [1]
279601
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Dr Aniruddh Deshpande
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Address [1]
279601
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John Hunter Hospital
Lookout Rd
New Lambton Heights NSW 2305
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Country [1]
279601
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
297948
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Sydney Children’s Hospitals Network Human Research Ethics Committee
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Ethics committee address [1]
297948
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The Children's Hospital at Westmead Locked Bag 4001 Westmead NSW 2145
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Ethics committee country [1]
297948
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Australia
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Date submitted for ethics approval [1]
297948
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01/08/2017
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Approval date [1]
297948
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12/12/2017
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Ethics approval number [1]
297948
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Summary
Brief summary
Transcutaneous electrical nerve stimulation (TENS) is an effective treatment method for overactive bladder and urge incontinence in children (de Gennaro et al., 2011; Barroso et al., 2011). The aim of the study is to analyse the effects of TENS on psychosocial outcomes,quality of life and lower urinary tract symptoms (LUTS) for treating overactive bladder in children by comparing changes in the strengths and difficulties questionnaire (SDQ) scores, the PinQ (paediatric incontinence quality of life) scores and lower urinary tract symptom scores (ICIQ-CLUTS – International Consultation on Incontinence Questionnaire – Pediatric Lower Urinary Tract Symptoms) before and after treatment with TENS for 3 months. The following hypotheses shall be examined: 1. Is there an improvement in psychological symptoms after three months of treatment with TENS? 2. Is there an improvement in quality of life scores after three months of treatment with TENS? 3. Is there a reduction in lower urinary tract symptoms after three months of treatment with TENS?
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Trial website
none
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Trial related presentations / publications
none yet
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Public notes
This study is part of an international collaboration, Data from the Australian sites will be also be compared with data from Germany and Brazil. Germany and Brazil have not registered the study.
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Contacts
Principal investigator
Name
75550
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A/Prof Patrina Caldwell
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Address
75550
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Centre for Kidney Research
The Children's Hospital at Westmead
Locked Bag 4001
Westmead NSW 2145
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Country
75550
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Australia
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Phone
75550
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+612 9845 3406
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Fax
75550
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+612 9845 1491
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Email
75550
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[email protected]
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Contact person for public queries
Name
75551
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Patrina Caldwell
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Address
75551
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Centre for Kidney Research
The Children's Hospital at Westmead
Locked Bag 4001
Westmead NSW 2145
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Country
75551
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Australia
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Phone
75551
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+612 9845 3406
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Fax
75551
0
+612 9845 1491
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Email
75551
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[email protected]
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Contact person for scientific queries
Name
75552
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Patrina Caldwell
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Address
75552
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Centre for Kidney Research
The Children's Hospital at Westmead
Locked Bag 4001
Westmead NSW 2145
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Country
75552
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Australia
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Phone
75552
0
+612 9845 3406
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Fax
75552
0
+612 9845 1491
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Email
75552
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
2263
Informed consent form
373123-(Uploaded-05-06-2019-13-52-48)-Study-related document.docx
2264
Study protocol
we are happy for the protocol to be publicly avail...
[
More Details
]
373123-(Uploaded-05-06-2019-13-53-24)-Study-related document.docx
2265
Ethical approval
373123-(Uploaded-05-06-2019-14-02-38)-Study-related document.pdf
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.
Download to PDF