Treatment of Stress Urinary Incontinence Via Smartphone
研究概览
详细说明
Female urinary incontinence (UI) is very common and affects up to one fourth of grownup women. It may reduce quality of life for those affected and costs for society are high. The most common type of urinary incontinence is SUI, i.e leakage when coughing, sneezing or jumping.
The recommended first line treatment is pelvic floor muscle training (PFMT)which leads to improvement or cure in two-thirds of patients. In addition, life style changes, such as weight loss when obese, smoking cessation and reduction of fluid intake if high is recommended.
There is a need for new , flexible and easily accessible treatment programmes for female urinary incontinence. In our previous study, we compared two treatment programmes for SUI without face-to-face contact: one internet based and one sent by post, both based on three months of PFMT. In this randomized controlled trial of 250 women aged 18-70 years, we found highly significant improvements (p<0.001) with large effect sizes (>0,8)concerning primary outcomes (symptoms and quality of life scores) but no significant differences between groups. Compared with the postal group, more participants in the internet group perceived they were much or very much improved (40.9% vs 26.5%, p<0.01, reported reduced usage of incontinence aids (59.5% vs 41.4%, p=0.02) and were satisfied with the treatment programme (84.8% vs 62.9%, p<0.001).
The selling of smartphones is increasing rapidly. About 75% of all cellphones sold in Sweden today are smartphones. Two million adults in Sweden have a smartphone. Many smartphone owners have at least one health app on their phone. Exercise, diet, and weight apps are the most popular types.
From our previous experience of an Internet-based programme, we have developed a treatment program designed for smartphone. The effect of the treatment programme will be evaluated after three months by comparing the effect in the "smartphone group" with the effect in the "waiting group".
Participants are consecutively recruited through our website. They answer an online screening survey with automated immediated response for initial screening of eligibility criteria. Informed consent and leakage diary (number of episodes of urinary leakage during 48 hours) are sent by post. After that, they answer a web questionnaire and finally they are interviewed by a researcher to confirm the diagnosis SUI and to ascertain that the patient is well informed of the study procedure.
Women are then randomized to either of the two groups. Women in the smartphone group get a smartphone application for iphone or android. Follow-up after three months with a web questionnaire and a leakage diary. After that the waiting group get their smartphone application.
We aim to recruit 120 women aged 18 and older via our website www.tät.nu. In the power calculation we assume that the improvement in the symptom score (ICIQ UI SF) and the QOL score (ICIQ luts QOL)in the smartphone group will be similar to the improvement we found in the postal group in our previous study. We also assume that the waiting group will improve in some extent.
To detect a difference between groups, power 80%, 2-side test and significance 0,05, group size as follow
ICIQ UI SF Smartphone group improves 2.9 (SD3,1) and waiting group 1,0 (SD2,0); 30 in each group
ICIQ luts QOL Smartphone group improves 4.6 (SD6,7) and waiting group 2.0(SD3.0), 35 in each group
PGI (patient´s global impression of improvement). 26,5% improves much or very much (smartphone) and 4% (waiting group):39 in each group
We expect a drop out rate of 33% and thus need approximately 120 persons, 60 in each group.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Umeå、瑞典、S-90185
- Umeå University
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- stress urinary incontinence
- leakage once a week or more often
- duration of symptoms for at least 6 months
- motivation and time to perform a 12 week long treatment with pelvic floor muscle training
- ability to read and write Swedish
- asset to smartphone
- possibility to send and receive email and asset to printer
- accept to be randomized to one of two groups; a treatment group or a waiting list group
Exclusion Criteria:
- participation in our previous internet study
- pregnancy
- former incontinence surgery
- known malignancy in lower abdomen
- difficulties with passing urine
- visual blood in urine
- intermenstrual bleeding
- severe psychiatric diagnosis
- neurological disease with affection on sensibility in legs or lower abdomen
- urge incontinence
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Smartphone treatment
Smartphone treatment with PFMT.
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A smartphone application with information on SUI, life style information, different programmes of PFMT with increasing severity, possibility to save statistics on training.
The treatment period is three months
|
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无干预:Waiting list
Waiting list for three months.
They receive the smartphone application after follow-up.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
International Consultation on Incontinence Modular Questionnaire Urinary Incontinence Short Form (ICIQ-UI SF)
大体时间:baseline, three months
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Three items on frequency, amount of leakage and overall impact.
Scoring 0-21, higher values indicating increasing severity
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baseline, three months
|
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International Consultation on Incontinence Modular Questionnaire Lower Urinary Tract Symptoms Quality of Life (ICIQ-LUTSqol)
大体时间:baseline, three months
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The instrument includes 19 items on the impact of the leakage.
All items are scored 1-4 (not at all/never, slightly/sometimes, moderately/often, a lot/all the time).
The overall score is 19-76, with higher values indicating increased impact on QOL.
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baseline, three months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Usage of Incontinence Aids
大体时间:three months
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Usage of incontinence aids during the last 4 weeks.
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three months
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Patient Satisfaction
大体时间:three months
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A self-rated question about if the current treatment was sufficient, with three response options
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three months
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Incontinence Episode Frequency (IEF)
大体时间:baseline, three months
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number of incontinence episodes per week
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baseline, three months
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Patient's Global Impression of Improvement Scale (PGI-I)
大体时间:three months
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A self-rated question that asks about the change experienced after treatment with 7 response options, ranging from "very much better" to "very much worse".
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three months
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合作者和调查者
调查人员
- 学习椅:Eva Samuelsson, MD, PhD、Department of Public Health and Clinical Medicine, Umeå University
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- VisareNorr301811
- JLL314561 (其他赠款/资助编号:The County council of Jämtland)
- FAS2008-0952 (其他赠款/资助编号:Swedish Council for Working Life and Social research)
- ALFVLL222081 (其他赠款/资助编号:Västerbotten County Council (ALF))
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