ID

16969

Beskrivning

ODM derived from: http://research.uic.edu/qip/toolbox/case-report-forms-crf. Template Name: Study Completion Form. QIP Case Report Forms, UIC Quality Improvement CRF, Office of the Vice Chancellor for Research. Center for Clinical and Translational Science, UIC University of Illinois at Chicago.

Länk

http://research.uic.edu/qip/toolbox/case-report-forms-crf

Nyckelord

  1. 2016-08-17 2016-08-17 -
Uppladdad den

17 augusti 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Study Completion Form: UIC Quality Improvement CRF

Study Completion Form: UIC Quality Improvement CRF

General Information
Beskrivning

General Information

Protocol Title
Beskrivning

Protocol Title

Datatyp

text

Site Number
Beskrivning

Site Number

Datatyp

integer

Subject ID
Beskrivning

Subject ID

Datatyp

integer

Visit Date
Beskrivning

Visit Date

Datatyp

date

Study Completion
Beskrivning

Study Completion

1. Date of final study visit
Beskrivning

1. Date of final study visit

Datatyp

date

2. Date of last known study intervention
Beskrivning

2. Date of last known study intervention

Datatyp

date

3. Primary reason for terminating participation in the study
Beskrivning

3. Primary reason for terminating participation in the study

Datatyp

text

If Other, please specify
Beskrivning

If Other, please specify

Datatyp

text

Comments
Beskrivning

Comments

Datatyp

text

I have reviewed all data contained on all pages of the case report and certify that they are accurate, complete, and a true reflection of the subject´s record.: PI Signature
Beskrivning

I have reviewed all data contained on all pages of the case report and certify that they are accurate, complete, and a true reflection of the subject´s record.: PI Signature

Datatyp

text

Date
Beskrivning

Date

Datatyp

date

PI Printed Name
Beskrivning

PI Printed Name

Datatyp

text

Similar models

Study Completion Form: UIC Quality Improvement CRF

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
General Information
Protocol Title
Item
Protocol Title
text
Site Number
Item
Site Number
integer
Subject ID
Item
Subject ID
integer
Visit Date
Item
Visit Date
date
Item Group
Study Completion
1. Date of final study visit
Item
1. Date of final study visit
date
2. Date of last known study intervention
Item
2. Date of last known study intervention
date
Item
3. Primary reason for terminating participation in the study
text
Code List
3. Primary reason for terminating participation in the study
CL Item
Completed study (1)
CL Item
Subject was determined after enrollment to be ineligible (Provide comments) (2)
CL Item
Subject withdrew consent (Provide comments) (3)
CL Item
Adverse Event (Complete the SAE form if applicable) (4)
CL Item
Lost to follow-up (5)
CL Item
Other (specify) (6)
CL Item
Unknown (7)
If Other, please specify
Item
If Other, please specify
text
Comments
Item
Comments
text
I have reviewed all data contained on all pages of the case report and certify that they are accurate, complete, and a true reflection of the subject´s record.: PI Signature
Item
I have reviewed all data contained on all pages of the case report and certify that they are accurate, complete, and a true reflection of the subject´s record.: PI Signature
text
Date
Item
Date
date
PI Printed Name
Item
PI Printed Name
text

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