It means that the particpants have

to participate, that they understand the

of the study, and they are fully aware that they can

at any given time. When one is unable to give consent, eg disabled or

there are special provisions required like

from the parents

. Researchers may not

any information about a specific partcipants

. In fact, any identifying data that IS stored must be

from the participants data

minimisation. This means that the research must avoid or minimise any potential

risks or harms. This also means tat if there is any

of harm this must be antciapted and

to the participants, again making sure they are aware they can

at any time. Also, if discomfort/harm does occur, the researcher must

or reversed if applicable and the harm must be

by the merit of research

. This is an issue as by definition, it denies the right of free and informed

as the P's are not fully aware of the nature of the study BUT you can receive permission to do this under strict circumstances

merit, meaning whether the study itself is

appropriate, and capable of

the intended means

discriminating

of the client, when there is a

obligation, if there is an immediate risk of

that can be avoided by disclosing info. Also, when in a provisional or supervisional scenario, one is allowed to disclose information with

as long as they conceal the clients (and all related parties)...

to confidentiality.