ID

16969

Description

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.

Link

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

Keywords

  1. 8/17/16 8/17/16 -
Uploaded on

August 17, 2016

DOI

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License

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
Description

General Information

Protocol Title
Description

Protocol Title

Data type

text

Site Number
Description

Site Number

Data type

integer

Subject ID
Description

Subject ID

Data type

integer

Visit Date
Description

Visit Date

Data type

date

Study Completion
Description

Study Completion

1. Date of final study visit
Description

1. Date of final study visit

Data type

date

2. Date of last known study intervention
Description

2. Date of last known study intervention

Data type

date

3. Primary reason for terminating participation in the study
Description

3. Primary reason for terminating participation in the study

Data type

text

If Other, please specify
Description

If Other, please specify

Data type

text

Comments
Description

Comments

Data type

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
Description

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

Data type

text

Date
Description

Date

Data type

date

PI Printed Name
Description

PI Printed Name

Data type

text

Similar models

Study Completion Form: UIC Quality Improvement CRF

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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