Written informed consent was obtained from all subjects after receiving an explanation of the study.
In this consent form an explanation of the study objectives and risks related to HLC collection were given, as well as the option for them to participate or not.
The interviews began with a consent process and an explanation of the study purpose.
After an explanation of the study, written informed consent will be obtained from each patient.
Subjects had to provide written informed consent after receiving an explanation of the study.
Those eligible were offered information leaflets and an explanation of the study by the CI (MED).
Consenting respondents were asked to sign an informed consent following an explanation of the study.
Written consent was obtained from all participants after an explanation of the study was provided.
The same form, which included an explanation of the study, was provided to all the participants.
Midwives were given an explanation of the study and were asked to give written consent.
