Survey: National Decade against Cancer (Germany): Difference between revisions

Revision as of 15:58, 15 May 2024

Go back to Germany page

Primary purpose: To engage the population and relevant stakeholders in cancer research, gathering their needs and perspectives to facilitate the successful translation of research findings into medical practice.

Sponsor, manager or home institution: Federal Ministry of Education and Research; Federal Ministry of Health and many others partners.

Type of information: Data Dictionary: National Decade against Cancer - Survey.

Data level: respondent level.

Number of records: 3.047 respondents.

Date range: 2019.

Cancer Areas of Interest: Unknown.

Data access: publicly available. Click here to access the public survey (general public) and [click here to access the science and care survey (professionals working in cancer research and healthcare)https://www.datenportal.bmbf.de/portal/opendata/PG_NDK_Umfrage_Wissenschaft_und_Versorgung_OnlineDialog.xlsx].

Contact information: Click here to access.

@@ Line 5: / Line 5: @@
 '''Sponsor, manager or home institution:''' [[dataOwner::Federal Ministry of Education and Research]]; [[dataOwner::Federal Ministry of Health]] and many others partners.
-'''Type of information:''' [[Data Dictionary: National Decade against Cancer - Survey]].
+'''Type of information:''' [[hasDataDictionary::Data Dictionary: National Decade against Cancer - Survey]].
-Public survey: Sex; Age class; Questions about place of residence; Cancers interests; insights into the public's awareness, interest, and involvement in cancer research; Participants' backgrounds; Perceptions of cancer research, information sources, and media coverage; The willingness of participants to contribute anonymized health data for research purposes and their past or potential involvement in cancer research projects. Science and care survey: Sex; their research or healthcare institution; Field of work; Roles and positions within the research or healthcare sector; The top five challenges facing patient-oriented and translational cancer research in Germany; Experiences and perspectives on involving patient representatives in cancer research projects, the phases of research where such involvement is deemed crucial; Types of projects where patient involvement is most important; Experiences with engaging community oncologists in cancer research; Challenges and potential improvements; Research findings to the public and opinions on media coverage of cancer research from a public and patient perspective.
-'''Data level:''' Respondent level.
+'''Data level:''' [[dataLevel::respondent level]].
-'''Number of Records:''' 3.047 respondents.
+'''Number of records:''' 3.047 respondents.
-'''Date Range:''' 2019.
+'''Date range:''' [[dataEnd::2019]].
 '''Cancer Areas of Interest:''' Unknown.
-'''Open data access:''' Public survey (general public) [https://www.datenportal.bmbf.de/portal/opendata/PG_NDK_Umfrage_Oeffentlichkeit_OnlineDialog.xlsx] and science and care survey (professionals working in cancer research and healthcare)[https://www.datenportal.bmbf.de/portal/opendata/PG_NDK_Umfrage_Wissenschaft_und_Versorgung_OnlineDialog.xlsx].
+'''Data access:''' [[dataAvailability::	publicly available]]. [https://www.datenportal.bmbf.de/portal/opendata/PG_NDK_Umfrage_Oeffentlichkeit_OnlineDialog.xlsx Click here to access the public survey (general public)] and [click here to access the science and care survey (professionals working in cancer research and healthcare)https://www.datenportal.bmbf.de/portal/opendata/PG_NDK_Umfrage_Wissenschaft_und_Versorgung_OnlineDialog.xlsx].
-'''Information/Contact for data request:''' Contact information [https://www.govdata.de/web/guest/kontakt].
+'''Contact information:''' [https://www.govdata.de/web/guest/kontakt Click here to access].