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临床试验/NL-OMON47306
NL-OMON47306招募中3 期

ong term effects of multidisciplinary assessment and pre-partum Pelvic Floor Muscle Group Treatment in adult gravid women with stress urinary incontinence compared to care-as-usual: a randomized controlled trial - motherfit pre-partum

niversiteit Maastricht0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • * adult gravid woman
  • * urinary incontinence (stress or mixed with predominant stress UI factor)
  • * motivated for participation in the motherfit program
  • * signed informed consent
  • * competent to speak and understand Dutch language and to read and fill in forms independent
  • * mApps on tablet (Apple or Android) or webApp available

排除标准

  • * UI prior to pregnancy, still existing during pregnancy
  • * high-risk pregnancy giving, resulting in a contra-indication for performing intensive PFM exercises (f.i. placenta praevia, vaginal blood loss, partus prematurus imminens)
  • * suffering from significant exercise limitations or co-morbidities (physical or psychological) that would restrain a woman from participation in motherfit (group) training
  • * history of chronic neurological disorders or diseases related to UI (f.i. multiple sclerosis, cerebro-vascular accident, diabetes mellitus)
  • * urinary tract infection (urine-sediment, urine culture)
  • * history of anti-incontinence or urogynecological surgery
  • * women who are expected to be lost to follow-up (e.g. because of a planned change of residency)
  • * recent pelvic physiotherapy (< 6 months)
  • * refusal to use a mApp or webApp

研究者

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