Postal questionnaire data collection pilot study - APPEAL pilot study

Completed

• Conditions: Specialty: Reproductive Health and Childbirth, Primary sub-specialty: General Gynaecology; Health Category: Renal and Urogenital; Disease/Condition: Other diseases of urinary system; Urological and Genital Diseases

• Registration Number: ISRCTN99859966
• Lead Sponsor: Birmingham Women’s & Children’s NHS Foundation Trust

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-09-10
• Study Completion: 2018-11-30
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 800

Inclusion Criteria

Women who have delivered under the care of a participating community midwife team during a defined period

Exclusion Criteria

Women who:
1. Are under 16 years of age at the point their notes are reviewed
2. Have a non-live baby on discharge home after birth
3. Have informed the study team that they do not wish to receive the questionnaire

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The response rate for completion of urinary stress incontinence to the full and split questionnaire processes. The process that optimises the response rate for collection of urinary stress incontinence rates will then be used in the subsequent cluster randomised controlled trial (APPEAL).

Secondary Outcome Measures

Name	Time	Method
<br> 1. Stress urinary and bowel incontinence rates at questionnaire completion (10-12 weeks postnatal), the former for use in sample size calculation for the subsequent cluster randomised controlled trial<br> 2. Intra-cluster correlation co-efficient (ICC) for primary outcome for use in the subsequent cluster randomised controlled trial<br>