跳至主要内容
临床试验/NCT03027986
NCT03027986撤回不适用

Evaluation of a Postural Rehabilitation Program Based on Sensory-motor Control in Men With Urinary Incontinence After Prostatectomy

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2017年10月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
116
试验地点
1
主要终点
Difference from baseline in urine leakage

研究概览

简要总结

Urinary incontinence (UI) is defined by the International Continence Society as "any involuntary loss of urine complained by the patient". The anatomical and histological specificities of the pelvic floor muscles (PFM) give them a key role in the control of urination but also in the control of postural stability. These activities are involuntary automatisms and the mechanisms that lead to post-prostatectomy stress urinary incontinence are not only due to the loss of voluntary contraction of the pelvic floor muscles. The mechanisms that lead to UI are more complex and may involve the loss of efficacy of all deep muscle stabilizing lumbo-pelvic region. Rehabilitation of pelvic floor muscles is recommended in the treatment of urinary incontinence after prostatectomy (Grade A), but there is a lack of evidence to define the best treatment regimen for PFM rehabilitation.

Two kinds of PFM rehabilitation are are commonly practiced by specialized physiotherapists.

  • The first one is made in individual box, in supine position. By analytic contractions of the PFM, (exercises of Kegel type) +/- associated with an instrumental biofeedback. This method used voluntary contractions of MPP.
  • The second is realized in various positions following a gravity progression, in individual and /or common room. This technique aims to restore a stabilization of the entire lumbo-pelvic region by postural recruitment involving synergistic contractions of the PFM.

These trials propose to compare these two rehabilitation programs on populations with postoperative follow-up of more than 12 months.

We chose to objectify the urine leaks with the pad test (weighing of the protections urinary over a period of 3 times 24h) which will be our main evaluation criterion. The home test pad of 3 times in 24 hours has been used by numerous studies and its reproducibility and reliability are established.

Urinary incontinence is a recognized factor of sedentary lifestyle, fatigue, impaired mental health and decreased of physical fitness. We therefore wish to observe these parameters for each of our two randomized groups

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 78 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Gender: Male
  • Between the age of 18 and 78 years
  • Patient who underwent prostatectomy more than 12 months ago but less than 10 years
  • 3x24h pad test over or equivalent to 10 grs
  • Persistent urinary incontinence beyond 12 month following prostatectomy
  • Patient affiliated to social security
  • Patient who submitted non-opposition for participation in the study

排除标准

  • Patients who underwent prostatectomy or other visceral surgery less than one year ago
  • Patient who underwent surgical treatment of urinary incontinence
  • Patient with urinary incontinence less than 10g
  • Surgery considered within two years of inclusion
  • Radio, hormone, or chemotherapy cured or in progress
  • Anticholinergic treatment less than 3 months ago
  • Patient with neurological or bladder disorders potentially involved in incontinence disorders
  • Vestibular or psychiatric pathology making limitations to carry out all the examinations provided for in the protocol
  • Patient unable to complete the planned 15 visits to physiotherapist
  • Patient participating in another clinical trial

研究组 & 干预措施

postural rehabilitation program based on sensory-motor control

Experimental

干预措施: postural rehabilitation program (Behavioral)

Standard physiotherapy

No Intervention

结局指标

主要结局

Difference from baseline in urine leakage

时间窗: 6 months

urine leakage will be measured using pad test

次要结局

  • Difference from baseline in The Berg balance scale test(6 months)
  • Difference from baseline in quality of life(6 months)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Evaluation of a Postural Rehabilitation Program... | 临床试验