A randomized clinical trial of urinary incontinence in older women: cost-effectiveness of protocolized assessment and evidence-based treatment
Completed
- Conditions
- involuntary loss of urineurinary incontinence10018188
- Registration Number
- NL-OMON31408
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 246
Inclusion Criteria
Patients are eligible for the study if they have symptoms of involuntary loss of urine, if they are able to fill in a questionnaire in Dutch, and if they have given informed consent
Exclusion Criteria
Patients will be excluded if they have urinary tract infections or overflow incontinence, are suffering from malignancies, are currently treated for urogynaecological conditions, have an indwelling catheter or are severely demented or in a poor physical condition (according to their GP). In cases of urinary tract infections subjects will be offered treatment and reconsidered at a later date if the incontinence persists.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method