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dc.contributor.authorDumoulin, Chantal
dc.contributor.authorMorin, Mélanie
dc.contributor.authorDanieli, Coraline
dc.contributor.authorCacciari, Licia P.
dc.contributor.authorMayrand, Marie-Hélène
dc.contributor.authorTousignant, Michel
dc.contributor.authorAbrahamowicz, Michal
dc.date.accessioned2024-08-12T15:45:38Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2024-08-12T15:45:38Z
dc.date.issued2020-08-03
dc.identifier.urihttp://hdl.handle.net/1866/33716
dc.publisherAmerican Medical Associationfr
dc.rightsCe document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed under a Creative Commons Attribution 4.0 International License.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/deed.fr
dc.titleGroup-based vs individual pelvic floor muscle training to treat urinary incontinence in older women : a randomized clinical trialfr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté de médecine. École de réadaptationfr
dc.identifier.doi10.1001/jamainternmed.2020.2993
dcterms.abstractImportance Urinary incontinence is one of the most prevalent health concerns experienced by older women (aged ≥60 years). Individual pelvic floor muscle training (PFMT) is the recommended first-line treatment for stress or mixed urinary incontinence in women, but human and financial resources limit its delivery. Whether group-based PFMT performs as well as individual PFMT in this population remains unclear. Objective To assess the efficacy of group-based PFMT relative to individual PFMT for urinary incontinence in older women. Design, Setting, and Participants The Group Rehabilitation or Individual Physiotherapy (GROUP) study is a single-blind, randomized, noninferiority trial conducted in 2 Canadian research centers, from July 1, 2012, to June 2, 2018. A total of 362 community-dwelling women aged 60 years or older with symptoms of stress or mixed urinary incontinence were enrolled. Interventions After an individual session conducted to learn how to contract pelvic floor muscles, participants completed 12-week PFMT as part of a group of 8 women (n = 178) or in individual sessions (n = 184). Main Outcomes and Measures The primary outcome measure was the percentage reduction in urinary incontinence episodes at 1 year, as reported in a 7-day bladder diary and relative to pretreatment baseline. Secondary outcomes included lower urinary tract–related signs, symptoms, and quality of life immediately following treatment and at 1 year. Per-protocol analysis was used. Results Among 362 women who were randomized (mean [SD] age, 67.9 [5.8] years), 319 women (88%) completed the 1-year follow-up and were included in the per-protocol analysis. Median percentage reduction in urinary incontinence episodes was 70% (95% CI, 44%-89%) in individual PFMT compared with 74% (95% CI, 46%-86%) in group-based PFMT. The upper boundary of the 95% CI for the difference in the percentage reduction in urinary incontinence episodes at 1 year was lower than the prespecified margin for noninferiority of 10% (difference, 4%; 95% CI, −10% to 7%; P = .58), confirming noninferiority. Individual PFMT and group-based PFMT had similar effectiveness for all secondary outcomes at 1 year. Adverse events were minor and uncommon. Conclusions and Relevance Results of the GROUP study suggest that group-based PFMT is not inferior to the recommended individual PFMT for the treatment of stress and mixed urinary incontinence in older women. Widespread use in clinical practice may help increase continence-care affordability and treatment availability.fr
dcterms.isPartOfurn:ISSN:2168-6106fr
dcterms.isPartOfurn:ISSN:2168-6114fr
dcterms.languageengfr
UdeM.ReferenceFournieParDeposantdoi:10.1001/jamainternmed.2020.2993fr
UdeM.VersionRioxxVersion publiée / Version of Recordfr
oaire.citationTitleJAMA internal medicinefr
oaire.citationVolume180fr
oaire.citationIssue10fr
oaire.citationStartPage1284fr
oaire.citationEndPage1293fr


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Ce document est mis à disposition selon les termes de la Licence Creative Commons
Paternité 4.0 International. / This work is licensed under a Creative Commons Attribution 4.0
International License.
Usage rights : Ce document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed under a Creative Commons Attribution 4.0 International License.