ID

16969

Descrição

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

Palavras-chave

  1. 17/08/2016 17/08/2016 -
Transferido a

17 de agosto de 2016

DOI

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Licença

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
Descrição

General Information

Protocol Title
Descrição

Protocol Title

Tipo de dados

text

Site Number
Descrição

Site Number

Tipo de dados

integer

Subject ID
Descrição

Subject ID

Tipo de dados

integer

Visit Date
Descrição

Visit Date

Tipo de dados

date

Study Completion
Descrição

Study Completion

1. Date of final study visit
Descrição

1. Date of final study visit

Tipo de dados

date

2. Date of last known study intervention
Descrição

2. Date of last known study intervention

Tipo de dados

date

3. Primary reason for terminating participation in the study
Descrição

3. Primary reason for terminating participation in the study

Tipo de dados

text

If Other, please specify
Descrição

If Other, please specify

Tipo de dados

text

Comments
Descrição

Comments

Tipo de dados

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
Descrição

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

Tipo de dados

text

Date
Descrição

Date

Tipo de dados

date

PI Printed Name
Descrição

PI Printed Name

Tipo de dados

text

Similar models

Study Completion Form: UIC Quality Improvement CRF

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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