Project Aura: Co-design of a Home-based Monitoring Service

Inclusion criteria: For patients: * Adequate English to participate in focus groups without an interpreter * Patients of the study site who are currently undergoing treatment for anaemia of CKD * Patients willing to participate in at least one or more 60-minute and ideally 90-minute focus groups at the designated study location, time and date. * Patients capable of providing informed consent before attending the first focus group For carers: * Should be the primary carer nominated by a patient who fulfils the inclusion criteria, this includes parents of affected children * Should be willing to participate in at least 60-minute and ideally 90-minute focus groups at the designated study location, time and date. * Carers can only participate in the study with the patient he/she is caring for. The patient has also to be involved in the study * Carers need to be capable of providing informed consent before attending the first focus group For healthcare professionals: * All clinicians need to be current employees of the study site * Doctors need to be employed at Specialist Registrar, Fellow or Consultant Level * Nurses of all grades are invited to participate but ideally need to have had some involvement in the outpatient care of CKD patients with anaemia All participants: * Should be willing to have the session's recorded audio, transcripts and analysed data from the focus groups shared with Entia. * should be willing to attend multiple 60 to 90 minute focus groups. * should be willing for unidentifiable photos and video footage to be taken during the interview. * Participants attending focus groups later in the development process must be comfortable consenting to finger prick testing/ assessing the ease of use of the test disposable Exclusion criteria: Patients: * Does not have adequate English to participate in focus group interviews without an interpreter. * Patients of the study site who are not currently undergoing treatment or have previously undergone treatment within the past 12 months. * Patients not willing to participate in at least 60-minute and ideally 90-minute focus group discussion at the designated study location, time and date. * Participant not capable of providing consent or have a suitable, legally acceptable representative present to provide consent before the focus group interview. For carers: * Is not the nominated primary carer of a patient who fulfils the inclusion criteria, this includes parents of affected children * Not paired with a patient that is involved in the study * Carers not willing to participate in at least a 60-minute and ideally 90-minute focus group discussion at the designated study location, time and date. For healthcare professionals: None.