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Self-management of stress urinary incontinence via a mobile app: two-year follow-up of a randomized controlled trial VICTORIA HOFFMAN1, LARS SÖDERSTRÖM2 & EVA SAMUELSSON1 1Department of Public Health and Clinical Medicine, Umeå University, Umeå, and 2Unit of Research, Education and Development – Östersund, Umeå University, Umeå, Sweden ACTA Obstetricia et Gynecologica Scandinavica Journal Club -Gynecology- October 2017 Edited by Francesco D’Antonio
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Introduction It is estimated that approximately 10–25% of women experience urinary incontinence. Urinary incontinence can significantly affect quality of life and generate large costs for society. Stress urinary incontinence (SUI), is a peculiar type of incontinence and it is defined as leakage of urine concurrent with coughing, sneezing, or physical exertion. Despite this, only 15% of women with SUI seek care. Pelvic floor muscle training (PFMT) is recommended as the first-line treatment for SUI. A recent systematic review concluded that the long-term success (defined as one year or more after treatment) of PFMT is between 41 and 85%, with a surgery rate of 4.9–58%. Women can perform PFMT without face-to-face contact and it has been reported that PFMT provided via the internet or mobile app is associated with marked improvements in several short and long term outcomes.
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Aim of the study To investigate the long-term effects of using a mobile app to treat stress urinary incontinence with a focus on pelvic floor muscle training.
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Material and Methods Study design: Follow-up investigation of women who took part in a randomized controlled trial conducted from March 2013 to October 2014 in Sweden. Mobile App: The Tät® mobile app contains information about SUI, lifestyle, and the pelvic floor, and it allows users to set reminders and save statistics. The mobile app presents PFMT exercises with increasing levels of difficulty (six basic and six advanced). The exercises include four different types of contractions in different combinations, and they are meant to be performed three times a day. Findings from the previous RCT: Women with SUI, aged 27–72 years, were randomized either to receive the mobile app at the beginning of the study period (app group, n = 62), or to wait three months to receive it (control group, n = 61). After three months, the reduction in symptoms [the International Consultation on Incontinence Modular Questionnaire Urinary Incontinence Short Form (ICIQUI SF)] and quality of life scores [International Consultation on Incontinence Modular Questionnaire Lower Urinary Tract Symptoms Quality of Life (ICIQ-LUTSqol)] were 3.9 and 4.8, respectively. These reductions were significantly greater than those achieved for the control group .
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Material and Methods
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Material and Methods Inclusion criteria: Women who received the mobile app following randomization in the previous study and who received a follow-up of two years. Primary outcome: Difference in score from baseline to the two-year follow-up in: ICIQ-UI SF (which measures symptom severity with a score of 0–21, with higher values indicating increasing severity). ICIQ-LUTSqol, (which measures condition-specific quality of life with a score of 19–76, with higher values indicating more affected quality of life). Secondary outcomes: Changes in answers to the PGI-I questionare. Proportion of women who had sought further treatment for SUI since joining the study. Changes in the use of incontinence protection products since the women joined the study. Changes in the proportion of women who felt they could contract their pelvic floor muscles correctly since joining the study. Statistical analysis: Student’s t-, Fisher, Mann–Whitney, Wilcoxon and McNemar’s test were used to analyse data.
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Results Of the 61 women who participated in the three-month follow-up of the original study, 46 responded at two years. There were no significant differences between responders and non-responders with respect to age, BMI, smoking, education, and the severity of incontinence at baseline
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Results The symptom severity score (ICIQ-UI SF) decreased significantly from baseline to the two-year follow-up, mean decrease 3.1 (95% CI 2.0–4.2). For condition-specific quality of life (ICIQ-LUTSqol), the mean decrease was 4.0 (95% CI 2.1–5.9).
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Results At the two-year follow-up, 66.7% of the women reported that their leakage had improved compared with baseline. The proportion of women who felt they could contract their pelvic muscles correctly at two years was significantly greater than at baseline (67.4% vs. 30.4%, p < 0.001). The use of incontinence protection products decreased significantly compared to baseline (p = 0.04).
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Limitations Absence of a control group. Small sample size. Participants may not be representative of the general population. Approximately 80% of women included, had studied at a university level. However, the educational level does not appear to be associated with the ability to understand instructions and perform PFMT.
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Conclusion Self-management of stress urinary incontinence with support from the Tät® app had significant and clinically relevant long-term effects and may serve as first-line treatment of this condition.
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