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Study of the Efficacy of 4 Treatments for Fecal Incontinence in Community-dwelling Women

2018年1月8日 更新者:Lluís Mundet、Hospital de Mataró

Study of the Efficacy of Treatment of Fecal Incontinence in Community-dwelling Women: Assessment of Individual Efficacy on Anorectal Physiology and Cortical Plasticity, Its Impact on Clinical Severity and on Quality of Life.

This is a RCT aimed to assessing efficacy of kegel exercises,biofeedback, electrostimulation and transcutaneous neuromodulation on women with fecal incontinence, measuring its impact on anorectal physiology, cortical plasticity, clmical severity and the quality of life.

研究概览

地位

完全的

条件

详细说明

Fecal incontinence is a prevalent condition with a major impact on quality of life. Currently four treatments are being used in clinical practice: Kegel exercises (K), biofeedback (BF), electrostimulation (ES) and transcutaneous neuromodulation (NM). Results in the literature are discordant and lack methodological rigour making scientific evidence weak.

The aim of this study is to assess the efficacy of these four treatments on community-dwelling women and their impact on anorectal physiology, on clinical severity and on QoL.

This is a randomized control trial. Patient physiology was studied with anorectal manometry and endoanal ultrasonography; clinical severity was assessed with Cleveland and St. Mark's scales, and QoL with the Faecal Incontinence Quality of Life (FIQL) and the EuroQol's EQ5D questionnaires. Urinary incontinence (UI) was also evaluated by means of International Consultation on Incontinence (ICIQ) score. Patients were randomized and assigned to K (control), BF+K, ES+K or NM+K, given active treatment for a 3-month period, and then evaluated again with identical tests and parameters to identify changes.

研究类型

介入性

注册 (实际的)

150

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Age higher than 18
  • To be woman
  • Have had incontinence episiodes at least from 6 month since the beginning of the study
  • Have had incontinence episodes during the last month prior the beginning of the study
  • The patient is able to understand the nature and impliations of the study and, therefore, to decide her participation.

Exclusion Criteria:

  • Not meeting inclusion criteria
  • Have very mild condition (Wexner <4)
  • To be unable to perform / understand the treatments properly
  • Being pregnant
  • To have used treatmets for fecal incontinence within the last six months prior to the start of the study
  • If, at reserarcher's criteria, the patient has not the proper conditions to perform and finish the treatments.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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:Kegel exercises
Pelvic floor exercises designed in the 1950s' by Arnold Kegel.
The aim is to compare how each treatment improves symptoms and quality of life and which physiologic mechanisms affects. The basal treatment which other therapies are compared to is Kegel.
实验性的:biofeedback
Biofeeback therapy to improve neuromuscular coordination and strengthen sphincter contractility.
The aim is to compare how each treatment improves symptoms and quality of life and which physiologic mechanisms affects. The basal treatment which other therapies are compared to is Kegel.
实验性的:electrostimulation
Administration of electric current with a specific device (stimulator) and through a vaginal prove, in order to improve pelvic floor contractility.
The aim is to compare how each treatment improves symptoms and quality of life and which physiologic mechanisms affects. The basal treatment which other therapies are compared to is Kegel.
实验性的:transcutaneous neuromodulation
Stimulation of tibial nerve with a specific electric current through a stimulator and surface electrodes
The aim is to compare how each treatment improves symptoms and quality of life and which physiologic mechanisms affects. The basal treatment which other therapies are compared to is Kegel.

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
clinical severity
大体时间:Changes of severity after 3 month-treatment
severity of the symptoms measured with Cleveland score
Changes of severity after 3 month-treatment
maximum anal resting pressure
大体时间:Changes maximum anal resting pressure after 3 month-treatment
pressure of the anal canal measured with mmHg
Changes maximum anal resting pressure after 3 month-treatment
maximum squeeze pressure
大体时间:Changes maximum squeeze pressure after 3 month-treatment
pressure on the anal canal when squeezing measured with mmHg
Changes maximum squeeze pressure after 3 month-treatment
rectal sensitivity
大体时间:changes in rectal balloon filling after 3 month-treatment
patient's rectal perception, measured with cm3 of distention of a rectal balloon
changes in rectal balloon filling after 3 month-treatment

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2013年2月1日

初级完成 (实际的)

2016年12月1日

研究完成 (实际的)

2017年3月1日

研究注册日期

首次提交

2017年11月29日

首先提交符合 QC 标准的

2018年1月8日

首次发布 (实际的)

2018年1月9日

研究记录更新

最后更新发布 (实际的)

2018年1月9日

上次提交的符合 QC 标准的更新

2018年1月8日

最后验证

2018年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • IF02-11/2012

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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