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Lower urinary tract symptoms in men: The TRIUMPH cluster RCT

Worthington, Jo; Frost, Jessica; Sanderson, Emily; Cochrane, Madeleine; Wheeler, Jessica; Cotterill, Nikki; MacNeill, Stephanie J; Noble, Sian; Avery, Miriam; Clarke, Samantha; Fader, Mandy; Hashim, Hashim; McGeagh, Lucy; Macaulay, Margaret; Rees, Jonathan; Robles, Luke; Taylor, Gordon; Taylor, Jodi; Thompson, Joanne; Lane, J Athene; Ridd, Matthew J; Drake, Marcus J

Lower urinary tract symptoms in men: The TRIUMPH cluster RCT Thumbnail


Authors

Jo Worthington

Jessica Frost

Emily Sanderson

Madeleine Cochrane

Jessica Wheeler

Profile image of Nikki Cotterill

N Nikki Cotterill Nikki.Cotterill@uwe.ac.uk
Professor of Long Term Conditions (Continence Care)

Stephanie J MacNeill

Sian Noble

Miriam Avery

Samantha Clarke

Mandy Fader

Hashim Hashim

Lucy McGeagh

Margaret Macaulay

Jonathan Rees

Luke Robles

Gordon Taylor

Jodi Taylor

Joanne Thompson

J Athene Lane

Matthew J Ridd

Marcus J Drake



Abstract

Conservative therapies are recommended as initial treatment for male lower urinary tract symptoms. However, there is a lack of evidence on effectiveness and uncertainty regarding approaches to delivery. The objective was to determine whether or not a standardised and manualised care intervention delivered in primary care achieves superior symptomatic outcome for lower urinary tract symptoms to usual care. This was a two-arm cluster randomised controlled trial. The trial was set in 30 NHS general practice sites in England. Participants were adult men (aged ≥ 18 years) with bothersome lower urinary tract symptoms. Sites were randomised 1 : 1 to deliver the TReatIng Urinary symptoms in Men in Primary Health care using non-pharmacological and non-surgical interventions trial intervention or usual care to all participants. The TReatIng Urinary symptoms in Men in Primary Health care using non-pharmacological and non-surgical interventions intervention comprised a standardised advice booklet developed for the trial from the British Association of Urological Surgeons' patient information sheets, with patient and expert input. Patients were directed to relevant sections by general practice or research nurses/healthcare assistants following urinary symptom assessment, providing the manualised element. The healthcare professional provided follow-up contacts over 12 weeks to support adherence to the intervention. The primary outcome was the validated patient-reported International Prostate Symptom Score 12 months post consent. Rather than the minimal clinically important difference of 3.0 points for overall International Prostate Symptom Score, the sample size aimed to detect a difference of 2.0 points, owing to the recognised clinical impact of individual symptoms. A total of 1077 men consented to the study: 524 in sites randomised to the intervention arm ( = 17) and 553 in sites randomised to the control arm ( = 13). A difference in mean International Prostate Symptom Score at 12 months was found (adjusted mean difference of -1.81 points, 95% confidence interval -2.66 to -0.95 points), with a lower score in the intervention arm, indicating less severe symptoms. Secondary outcomes of patient-reported urinary symptoms, quality of life specific to lower urinary tract symptoms and perception of lower urinary tract symptoms all showed evidence of a difference between the arms favouring the intervention. No difference was seen between the arms in the proportion of urology referrals or adverse events. In qualitative interviews, participants welcomed the intervention, describing positive effects on their symptoms, as well as on their understanding of conservative care and their attitude towards the experience of lower urinary tract symptoms. The interviews highlighted that structured, in-depth self-management is insufficiently embedded within general practitioner consultations. From an NHS perspective, mean costs and quality-adjusted life-years were similar between trial arms. The intervention arm had slightly lower mean costs (adjusted mean difference of -£29.99, 95% confidence interval -£109.84 to £22.63) than the usual-care arm, and a small gain in quality-adjusted life-years (adjusted mean difference of 0.001, 95% confidence interval -0.011 to 0.014). The intervention showed a small, sustained benefit for men's lower urinary tract symptoms and quality of life across a range of outcome measures in a UK primary care setting. Qualitative data showed that men highly valued the intervention. Intervention costs were marginally lower than usual-care costs. Limitations of the study included that trial participants were unmasked, with limited diversity in ethnicity and deprivation level. Additional research is needed to assess the applicability of the intervention for a more ethnically diverse population.. This trial is registered as ISRCTN11669964. This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: 16/90/03) and is published in full in ; Vol. 28, No. 13. See the NIHR Funding and Awards website for further award information.

Journal Article Type Article
Acceptance Date Mar 26, 2024
Online Publication Date Mar 31, 2024
Publication Date Mar 31, 2024
Deposit Date Mar 27, 2024
Publicly Available Date Apr 4, 2024
Journal Health technology assessment (Winchester, England)
Print ISSN 1366-5278
Electronic ISSN 2046-4924
Publisher NIHR Journals Library
Peer Reviewed Peer Reviewed
Volume 28
Issue 13
Pages 1-162
DOI https://doi.org/10.3310/GVBC3182
Keywords CLUSTER RANDOMISED CONTROLLED TRIAL, General Practitioners, GENERAL PRACTICE, LOWER URINARY TRACT SYMPTOMS, Lower Urinary Tract Symptoms - therapy, Humans, Allied Health Personnel, PRIMARY CARE, TRIUMPH, PATIENT EXPERIENCE, SELF-MANAGEMENT, QUALITATIVE, P
Public URL https://uwe-repository.worktribe.com/output/11847389
Additional Information Free to read: This content has been made freely available to all.; contractual_start_date: 11-2017; editorial review begun: 08-2021; Accepted for publication: 02-2022

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