Postpartum urinary incontinence Urological and Genital Diseases
Conditions
Interventions
The intervention in this pilot and feasibility cluster randomized controlled trial comprises an antenatal midwife training package aimed at enhancing midwife ability and motivation to inform and suppo
Sponsors
Birmingham Women's and Children's NHS Foundation Trust
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: All women who receive antenatal care from a participating community midwifery team (cluster) during the trial period
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Dichotomous feasibility measures, such as recruitment and questionnaire return rates, as well as data completeness, will be reported as numbers and percentages 2. The feasibility and pilot cluster trial questionnaire will provide data to facilitate estimation of the sample size required for a future RCT 3. Outcome data on urinary incontinence and PFME will be collected from women at 10-12 weeks postnatally | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
England, United Kingdom
Contacts
Public ContactWilliam McKinnon
Outcome results
None listed