Stimulation of the tibial nerve—a randomised trial for urinary problems associated with Parkinson’s—the STARTUP trial

Author:

McClurg Doreen1,Elders Andrew1,Hagen Suzanne1,Mason Helen2,Booth Jo3,Cunnington Anne-Louise4,Walker Richard5,Deane Katherine6,Harari Danielle7,Panicker Jalesh8,Stratton Susan1,McArthur Jaclyn2,Sellers Ceri1,Collins Marissa2

Affiliation:

1. NMAHP RU , Glasgow Caledonian University, Glasgow G4 0BA , UK

2. Yunus Centre for Social Business and Health , Glasgow Caledonian University, Glasgow G4 0BA , UK

3. Scholl of Health & Life Sciences , Glasgow Caledonian University, Glasgow G4 0BA , UK

4. The New Stobhill Hospital – NHSGGC , G21 3UW

5. Northumbria Healthcare NHS Foundation Trust , NE25 0QJ

6. School of Nursing Sciences , University of East Anglia, NR4 7TJ, Norwich

7. Guy’s & St Thomas Hospital NHS Foundation Trust , SE1 7EH, London

8. University College London Hospitals NHS Foundation Trust , WC1E 6BT, London

Abstract

Abstract Background non-motor symptoms such as bladder dysfunction are common (80%) in people with Parkinson’s increasing the risk for falls with a negative impact on health-related costs and quality of life. We undertook STARTUP to evaluate the clinical and cost-effectiveness of using an adhesive electrode to stimulate the transcutaneous tibial nerve stimulation (TTNS) to treat bladder dysfunction in people with Parkinson’s disease (PD). Study design, materials and methods: STARTUP was a parallel two-arm, multi-centre, pragmatic, double-blind, randomised controlled trial. Each participant attended one clinic visit to complete consent, be randomised using a computer-generated system and to be shown how to use the device. The trial had two co-primary outcome measures: International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form and the International Prostate Symptom Score (IPSS). These were completed at baseline, 6 and 12 weeks. A bladder frequency chart and resource questionnaire were also completed. Results two hundred forty two participants were randomised. About 59% of participants were male, the mean age was 69 years and mean time since diagnosis was 6 years. Questionnaire return rate was between 79 and 90%. There was a statistically significantly lower score in the active group at 6 weeks in the IPSS questionnaire (mean difference (Standard deviation, SD) 12.5 (6.5) vs 10.9 (5.5), effect size −1.49, 95% CI −2.72, −0.25). There was no statistically significant change in any other outcome. Conclusion TTNS was demonstrated to be safe with a high level of compliance. There was a significant change in one of the co-primary outcome measures at the end of the treatment period (i.e. 6 weeks), which could indicate a benefit. Further fully powered RCTs are required to determine effective treatments.

Funder

Parkinson UK

Dunhill Medical Trust

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging,General Medicine

Reference36 articles.

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2. Lower urinary tract symptoms in Parkinson's disease: prevalence, aetiology and management;McDonald;Parkinsonism Relat Disord,2017

3. Urinary incontinence and pelvic organ prolapse in women: management;NICE

4. Anticholinergic drug exposure and the risk of dementia: a nested case-control study;Coupland;JAMA Intern Med,2019

5. Botulinum toxin a for overactive bladder and detrusor muscle overactivity in patients with Parkinson’s disease and multiple system atrophy;Giannantoni;J Urol,2009

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