A study of maternity service users’ and providers’ experience of the Tommy’s Clinical Decision Tool in four early adopter sites, and identification of factors to inform successful implementatio
- Conditions
- Pregnancy complicationsPregnancy and Childbirth
- Registration Number
- ISRCTN13498237
- Lead Sponsor
- King's College London
- Brief Summary
2022 Protocol article in https://pubmed.ncbi.nlm.nih.gov/35971107/ (added 16/08/2022)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 1298
Current inclusion criteria as of 17/10/2022:
Work Package 1: Healthcare professionals/providers providing and/or managing maternity care in participating Trusts
Work Package 2: Women booking for maternity care at participating Trusts who have:
1. Registered for the Tommy's Clinical Decision Tool
2. Given permission for researchers to contact them
3. Consented to participate in this study.
Work Package 3: Aggregate data from women booking for maternity care at participating Trusts who have registered for the Clinical Decision Tool
_____
Previous inclusion criteria:
Work Package 1: Healthcare professionals/providers providing and/or managing maternity care in participating Trusts
Work Package 2: Women booking for maternity care at participating Trusts who have:
1. Registered for the Clinical Decision Tool
2. Given permission for researchers to contact them following the birth of their baby
Work Package 3: Aggregate data from women booking for maternity care at participating Trusts who have registered for the Clinical Decision Tool
Current exclusion criteria as of 17/10/2022:
Work Package 1: unwilling to participate in the study
Work Package 2:
1. Women who have not registered to use the tool during this pregnancy
2. Those unwilling to give permission for researchers to contact them.
Work Package 3: women who have indicated their NHS data should not be used for research purposes
_____
Previous exclusion criteria:
Work Package 1: unwilling to participate in the study
Work Package 2: unwilling to participate in the study
Work Package 3: women who have indicated their NHS data should not be used for research purposes
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method