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Clinical Trials/NL-OMON47366
NL-OMON47366
Recruiting
Phase 3

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

niversiteit Maastricht0 sites90 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
post partum incontinence
Sponsor
niversiteit Maastricht
Enrollment
90
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • \* adult woman after vaginal delivery
  • \* 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

Exclusion Criteria

  • \- UI prior to pregnancy, still existing after vaginal delivery
  • \* 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

Outcomes

Primary Outcomes

Not specified

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