Pilot study for the project: 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-OMON30406
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
Women 55 years or older
Suffering from urinary incontinence: involuntary loss of urine two or more times a month
Able to fill in a questionnaire
Informed consent
Exclusion Criteria
Indwelling urinary cateter
Urogynaecological malignancies
Demented
Poor physical condition
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>In the pilot the recruitment procedure is studied, the quality of the data from<br /><br>the questionnaires and the micturition diary and the logistics of the<br /><br>urogynaecological examination. Also, the time investment is measured.</p><br>
- Secondary Outcome Measures
Name Time Method <p>niet van toepassing</p><br>