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Randomized Controlled Trial
A single-blind, randomized controlled trial to evaluate the effectiveness of transcutaneous tibial nerve stimulation (TTNS) in Overactive Bladder symptoms in women responders to percutaneous tibial nerve stimulation (PTNS).
- Miguel Martin-Garcia and Jennifer Crampton.
- Physiotherapy Department, Liverpool Women's NHS Trust, Crown Street, Liverpool, L8 7SS, UK. Electronic address: miguel.martin-garcia@lwh.nhs.uk.
- Physiotherapy. 2019 Dec 1; 105 (4): 469-475.
ObjectivesTo evaluate the effectiveness of transcutaneous tibial nerve stimulation (TTNS) compared to percutaneous tibial nerve stimulation (PTNS) in sustaining symptom improvement over a 6-month period in women with idiopathic Overactive Bladder (OAB) who had responded to an initial 12-week course of PTNS.DesignRandomized, active-controlled trial.ParticipantsTwenty-four women diagnosed with idiopathic OAB successfully treated with PTNS were included in this study.InterventionsTwelve subjects were allocated to receive monthly sessions of PTNS for six months, and twelve subjects followed a flexible home-based TTNS regime after instruction on the use of a TENS device for the same follow-up time.OutcomesParticipants were assessed at six weeks, three months and six months after completing the initial course of PTNS. Primary outcomes were changes from baseline in urinary frequency, number of episodes of urgency and number of episodes of urge urinary incontinence (UUI). Subjectively reported severity of symptoms and quality of life (QoL) were assessed using the validated OAB questionnaire (OAB-q).ResultsUrinary frequency, episodes of urinary urgency and episodes of UUI did not change significantly between baseline and six months in either group. Similarly, OAB-q scores for severity of symptoms and QoL were maintained within both arms for the duration of the study. There were no statistically significant differences between the groups in any of the outcome measures at any of the study points.ConclusionTTNS is effective in the maintenance of symptom improvement in women with OAB who had positively responded to a course of 12 weekly PTNS sessions. The trial was registered in the Clinicaltrials.gov PRS database (Identifier: NCT02377765).Copyright © 2018. Published by Elsevier Ltd.
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