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Study

19 forms  
Note: This form is used to record important data describing study conditions. This information will be the same for all documented cases, unless there are changes to the study conditions over time.
Description

Note: This form is used to record important data describing study conditions. This information will be the same for all documented cases, unless there are changes to the study conditions over time.

Study affiliation
Description

Study affiliation

Which TTU/TI does the study belong to?
Description

STUDY_TTUTI_AFFILIATION

Data type

text

Which other TTU/TI does the study belong to?
Description

STUDY_TTUTI_AFFILIATION_OTHER

Data type

text

Name of the study/cohort in which the patient was included.
Description

STUDY_NAME

Data type

text

Which other cohort/study does the data belong to?
Description

STUDY_NAME_OTHER

Data type

text

Study site
Description

Study site

From which location is the study being conducted?
Description

STUDY_SITE

Data type

text

From which other location(s) will the study be conducted?
Description

STUDY_SITE_OTHER

Data type

text

Declaration of consent (general)
Description

Declaration of consent (general)

Which authorizations can be found in the consent form of the study?
Description

STUDY_CONSENT_GEN

Data type

text

Which other authorizations can be found in the declaration of consent for the study?
Description

STUDY_CONSENT_GEN_OTHER

Data type

text

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Similar models

Study

19 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Note: This form is used to record important data describing study conditions. This information will be the same for all documented cases, unless there are changes to the study conditions over time.
Item Group
Study affiliation
Item
Which TTU/TI does the study belong to?
text
CL.65
Code List
Which TTU/TI does the study belong to?
CL Item
TI Academy (TI_AD)
CL Item
TI African Partner Institutions (TI_API)
CL Item
TI Biobanking (TI_BB)
CL Item
TI Bioinformatics Platform (TI_BP)
CL Item
TI Clinical Trial Unit (TI_CTU)
CL Item
TI Epidemiology (TI_EPI)
CL Item
TI Novel Antivirals (TI_NA)
CL Item
TI Product Development Unit (TI_PDU)
CL Item
TI Pathogen Repository (TI_PR)
CL Item
TTU Emerging Infections (TTU_EI)
CL Item
TTU Gasttrointestinal Infections (TTU_GII)
CL Item
TTU HAARBI (TTU_HA)
CL Item
TTU Hepatitis (TTU_HEP)
CL Item
TTU HIV (TTU_HIV)
CL Item
TTU Infections of immunocompromised Host (TTU_IICH)
CL Item
TTU Malaria (TTU_MAL)
CL Item
TTU Novel Antibiotics (TTU_NA)
CL Item
TTU Tuberculosis (TTU_TUB)
CL Item
Other TTU/TI (OTHER)
STUDY_TTUTI_AFFILIATION_OTHER
Item
Which other TTU/TI does the study belong to?
text
Item
Name of the study/cohort in which the patient was included.
text
CL.66
Code List
Name of the study/cohort in which the patient was included.
CL Item
DZIF tissue bank (CRYO)
CL Item
Controlled Human Malaria Infection (LACHMI)
CL Item
COVID autopsy register (COVT)
CL Item
Eppstein Barr Virus (KS)
CL Item
Fever Without Score (FWS)
CL Item
Fever Without Score - Children (FWSC)
CL Item
Hepatitis-Kohorte (HBV)
CL Item
HIV-cohort (HIV)
CL Item
TIARA: MDRO colonization in complex surgical patients (TIARA)
CL Item
Transplant-Cohort (TX)
CL Item
Tuberculosis (TBC)
CL Item
Other cohort/study (OTHER)
STUDY_NAME_OTHER
Item
Which other cohort/study does the data belong to?
text
Item Group
Study site
Item
From which location is the study being conducted?
text
CL.99
Code List
From which location is the study being conducted?
CL Item
African Partner Site (AFRP)
CL Item
Bonn (BN)
CL Item
Borstel (BOR)
CL Item
Bunswick (BS)
CL Item
Brunswick - DSMZ (BSDSMZ)
CL Item
Duesseldorf (DUE)
CL Item
Giessen (GI)
CL Item
Hanover (H)
CL Item
Heidelberg (HD)
CL Item
Hamburg University (HH)
CL Item
Hamburg (BNI) (HHBNI)
CL Item
Hamburg (UKE) (HHUKE)
CL Item
Luebeck (HL)
CL Item
Cologne (K)
CL Item
Marburg (MR)
CL Item
Munich (LMU) (MLMU)
CL Item
Munich (TUM) (MTUM)
CL Item
Riems (RIEMS)
CL Item
Tuebingen (TUE)
CL Item
Other location (OTHER)
STUDY_SITE_OTHER
Item
From which other location(s) will the study be conducted?
text
Item Group
Declaration of consent (general)
Item
Which authorizations can be found in the consent form of the study?
text
CL.68
Code List
Which authorizations can be found in the consent form of the study?
CL Item
Biospecimen collection permitted (BIO)
CL Item
Contacting co-treaters permitted (CC)
CL Item
Release of health insurance data (HI)
CL Item
Recontacting patients permitted (RP)
CL Item
Release transfer EU abroad (EU)
CL Item
Release for transfer to non-EU countries (NEU)
CL Item
Release for commercial use (CU)
CL Item
Further release(s) (OTHER)
STUDY_CONSENT_GEN_OTHER
Item
Which other authorizations can be found in the declaration of consent for the study?
text
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