ID

16667

Descripción

ODM Form derived from: https://ictr.wisc.edu/CaseReptTempt. Template Name: Subject Off Study. Case Report Form (CRF)/Source Document templates were created for University of Wisconsin-Madison researchers. These templates are consistent with the FDA's CDASH (Clinical Data Acquisition Standards Harmonization) standards. The CDASH standards identify those elements that should be captured on a Case Report Form (CRF). The forms serve only as templates, and must be edited to meet the study data collection needs as described in the protocol.

Link

https://ictr.wisc.edu/CaseReptTempt

Palabras clave

Versiones (3)
  1. 30/7/16 30/7/16 -
  2. 25/11/16 25/11/16 -
  3. 20/6/18 20/6/18 - Julian Varghese
Subido en

30 de julio de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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Subject Off Study: CRF Wisconsin Madison

Inglés

Subject Off Study: CRF Wisconsin Madison

1 formularios  
Header
Descripción

Header

PI Name
Descripción

PI Name

Tipo de datos

text

IRB Number
Descripción

IRB Number

Tipo de datos

integer

Short Title
Descripción

Short Title

Tipo de datos

text

Subject Initials
Descripción

Subject Initials

Tipo de datos

text

Subject ID
Descripción

Subject ID

Tipo de datos

integer

Date
Descripción

Date

Tipo de datos

date

Subject Off Study
Descripción

Subject Off Study

Date subject went Off Study
Descripción

Date

Tipo de datos

date

Last visit completed
Descripción

Last visit

Tipo de datos

text

Indicate the primary reason the subject is no longer participating in the study
Descripción

Primary reason

Tipo de datos

text

Was subject treatment unblinded?
Descripción

Was subject treatment unblinded?

Tipo de datos

text

Additional explanation required:
Descripción

Additional explanation required

Tipo de datos

text

Form completed by
Descripción

Form completed by

Tipo de datos

text

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Similar models

Subject Off Study: CRF Wisconsin Madison

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Header
PI Name
Item
PI Name
text
IRB Number
Item
IRB Number
integer
Short Title
Item
Short Title
text
Subject Initials
Item
Subject Initials
text
Subject ID
Item
Subject ID
integer
Date
Item
Date
date
Item Group
Subject Off Study
Date
Item
Date subject went Off Study
date
Item
Last visit completed
text
Last visit
Code List
Last visit completed
CL Item
Screening visit (1)
CL Item
Visit 1 (2)
CL Item
Visit 2 (3)
Item
Indicate the primary reason the subject is no longer participating in the study
text
Primary reason
Code List
Indicate the primary reason the subject is no longer participating in the study
CL Item
Study Activities Completed (1)
CL Item
Subject Withdrawn (by subject) PRIOR to enrollment (i.e. subject deemed eligible but declined participation, etc.) Additional explanation required.  (2)
CL Item
Subject Withdrawn (by subject) AFTER enrollment (i.e. due to personal time constraints, etc.) Additional explanation required.  (3)
CL Item
Subject Withdrawn (by PI or study team) PRIOR to enrollment (i.e. subject deemed inappropriate for study participation by the PI or study team, explain below) (4)
CL Item
Subject Withdrawn (by PI or study team) AFTER enrollment (i.e. identification of disease/condition after enrollment that warrants withdrawal, participant was determined to be ineligible after enrollment etc.) (5)
CL Item
Adverse Events/Side effects/Complications (complete Adverse Tracking Log) Additional explanation required.  (6)
CL Item
Other. Additional explanation required. (7)
Item
Was subject treatment unblinded?
text
Was subject treatment unblinded?
Code List
Was subject treatment unblinded?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Applicable (3)
Additional explanation required
Item
Additional explanation required:
text
Form completed by
Item
Form completed by
text
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