CLINICAL RESEARCH

BASIC REQUIREMENTS TO OBTAIN THE SUPPORT OF EDTNA/ERCA IN RESEARCH ACTIVITIES

Step 1
- To be a current member of the association
- To submit the research protocol to the EDTNA/ERCA Research Group
- The RG will evaluate the protocol and will submit to the EDTN/ERCA Executive Committee for final approval.

Step 2
Once the research protocol is approved, the Principal Investigator formally agrees; 
- To collaborate with the Chair and the Data Manager of the EDTNA/ERCA Research Group

- Formally agrees to share the final results of the study with EDTNA/ERCA
- In case of publication of the results, the Principal Investigator formally agrees to add members of the EDTNA/ERCA Research Group or EDTNA/ERCA Executive Committee who have contributed substantially to the study, as co-author and declare the support of the EDTNA/ERCA


PROJECTS

'Nurse-perceived facilitators and barriers to palliative care in patients with end-stage kidney disease:an international multi-centre Delphi-survey' 

'Awareness, understanding and treatment practices among health care professionals involved in managing cachexia in patients with End-Stage Kidney Disease (in collaboration with the Queen’s University Belfast)'

EDTNA/ERCA Secretariat

Källstorps Gård / Högs Byväg 118 / SE-246 55 Löddeköpinge / Sweden
Phone: +46 46 70 96 24 / secretariat@edtnaerca.org

Legal Venue

EDTNA/ERCA, Seestrasse 91, CH 6052 Hergiswil, Switzerland