We'd like your feedback
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Dr
Carol
Kingdon
ckingdon@liverpool.ac.uk
Carol
Kingdon
C.Kingdon@liverpool.ac.uk
Abi
Merriel
abi.merriel@liverpool.ac.uk
Complications of labour and deliveryDelivery
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
Enabling women and birthing people to make decisions about their care by providing them with the necessary information to make decisions is vital. In this study we will build a consensus around the core information that should be provided about induction of labour and caesarean birth, we will do this separately for each topic. To do this we will review existing leaflets and literature, analyse existing data from interviews and carry out an online survey of parents, health and medicolegal professionals, and other interested groups. Once we have collected all of the possible information points, we will develop a survey, test it with users, and then recruit participants, from the previously mentioned groups, to identify how important each of the information elements is to them. We will undertake two rounds of this survey with important or controversial items going through to the second round, to ensure that the items included in the final list are the most important ones. We will finalise the core information sets at a consensus meeting of stakeholders.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Cross-sectional;
You can take part if:
You may not be able to take part if:
Women: Women who are under the age of 16. Women who are not able to give informed consent to participate in the study and women who do not understand/read one of the study languages.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Dr
Carol
Kingdon
ckingdon@liverpool.ac.uk
Carol
Kingdon
C.Kingdon@liverpool.ac.uk
Abi
Merriel
abi.merriel@liverpool.ac.uk
The study is sponsored by University of Liverpool and funded by NIHR Academy .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 55397
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
