It should be noted that all the data about risk perception, attitudes and beliefs were provided at baseline before randomisation and any recall.
Written informed consent was provided by all participants before randomisation.
Written informed consent was provided by the participants before randomisation.
A randomisation schedule was provided to the investigator and in accordance with the randomisation numbers; the subject received the study treatment regimen assigned to the corresponding randomisation number.
However, no further information was provided regarding who performed the randomisation, use of blinding, sequence generation or treatment allocation.
This should also ensure that participants are providing informed consent and are fully committed and motivated to take part in the study before randomisation.
In open randomised trials, preferences should be ascertained before randomisation.
Baseline HRQoL questionnaires had to be completed before randomisation.
The baseline questionnaires and demographics will be registered before randomisation.
Baseline eligibility data will be required before randomisation.
The initial baseline survey will be conducted before randomisation.
