1.how will you put the principle of informed consent into practice
2.have you informed all participants that are taking part in a study or are involved init
3.how will you ensure that the participants do not suffer any disadvantages or damages from the study or from taking part in it
4.how will you make sure that the participants in a control group do not suffer any dis ad vantage from the intervention they did not receive
5.how will you guarantee the voluntarism of the participation
6.how will you sure that children or cognitively impaired people have agreed to being interviewed that not merely the consent of caregivers was obtained
7.how will you organize the anonymization of the data and how will you deal with the issues of data protection in the study
8.how will you take these issues into account for the storage of the data and in presenting the results
9.have you checked you method of proceeding against the relevant ethical code
10.if so which problems became evident here
11.is a statement from an ethics committee necessary for you study and so have you obtained it
12.how will the project conform to requirements formulated in this process
13.what is the novelty in the expected results which justifies doing your project
14.can you specify the expected results