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NCT06255015 Clinical Trial

Breastfeeding Planning Card Trial in Scotland

Breastfeeding Clinical Trial

— CARRDS  

Official title:
Breastfeeding Planning Card Feasibility Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06255015
Other study ID # IRAS: 316125
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2023
Est. completion date July 31, 2024

Study information
Verified date February 2024
Source University of Stirling
Contact David Comerford
Phone 01786 467370
Email david.comerford@stir.ac.uk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the efficacy of a "breastfeeding toolkit" card delivered as part of antenatal care in promoting breastfeeding maintenance.

Description:

The project is an evaluation of an intervention that will start on January 1 2024. From January 1 2024 through to March 31st 2024 midwives will present to patients attending their 24 week antenatal appointment a breastfeeding toolkit card. The trial compares breastfeeding rates across patients who receive the card and those whose 24-week antenatal appointment occurred in the three months October 1 2023 - December 31 2023.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date July 31, 2024
Est. primary completion date October 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 17 Years and older
Eligibility Inclusion Criteria: - Pregnant women in NHS Grampian Exclusion Criteria: None

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Breastfeeding toolkit card
The card is delivered at 24 weeks and is also referred to in the 32 and 36 week antenatal meetings. It will also be referred to in the first 24 hours post-partum and in home visits.

Locations
Country Name City State
United Kingdom University of Stirling Stirling Stirlingshire

Sponsors (2)
Lead Sponsor Collaborator
University of Stirling NHS Grampian

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary breastfeeding rates at 6-8 weeks post-partum Proportion of women recorded as breastfeeding by their home visitor at 6-8 weeks post-partum 6-8 weeks
Secondary breastfeeding rates at 10-14 days post-partum Proportion of women recorded as breastfeeding by their home visitor at 10-14 days post-partum 10-14 days
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