ID

16969

Descripción

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

Palabras clave

  1. 17/8/16 17/8/16 -
Subido en

17 de agosto de 2016

DOI

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Licencia

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
Descripción

General Information

Protocol Title
Descripción

Protocol Title

Tipo de datos

text

Site Number
Descripción

Site Number

Tipo de datos

integer

Subject ID
Descripción

Subject ID

Tipo de datos

integer

Visit Date
Descripción

Visit Date

Tipo de datos

date

Study Completion
Descripción

Study Completion

1. Date of final study visit
Descripción

1. Date of final study visit

Tipo de datos

date

2. Date of last known study intervention
Descripción

2. Date of last known study intervention

Tipo de datos

date

3. Primary reason for terminating participation in the study
Descripción

3. Primary reason for terminating participation in the study

Tipo de datos

text

If Other, please specify
Descripción

If Other, please specify

Tipo de datos

text

Comments
Descripción

Comments

Tipo de datos

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
Descripción

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 datos

text

Date
Descripción

Date

Tipo de datos

date

PI Printed Name
Descripción

PI Printed Name

Tipo de datos

text

Similar models

Study Completion Form: UIC Quality Improvement CRF

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