CONCL
Table Description:
Detailed notes for this table are included below.
1.0 Description: Conclusion of Study Participation
View Source CRFs
1.0 CRFs: Click on any PAG_NAME link below to be taken to the CRF used in the PPMI 1.0 Study.
2.0 CRFs: Click on any PAG_NAME link below to be taken to a screenshot of how this eCRF is currently implemented in the PPMI 2.0 Study.
2.0 Data Dictionary
Table Constraints:
2.0 Code Book
ITM_NAME |
CODE |
DECODE_1.0 |
|---|---|---|
COMPLT |
0 |
No |
COMPLT |
1 |
Yes |
WDRSN |
1 |
Adverse Event (complete AE Log) |
WDRSN |
2 |
Lost to follow-up |
WDRSN |
3 |
Subject withdrew consent (specify) |
WDRSN |
4 |
Pregnancy |
WDRSN |
5 |
Protocol violation |
WDRSN |
6 |
Death of subject |
WDRSN |
7 |
Investigator decision (specify) |
WDRSN |
9 |
Clinical Monitor decision (specify) |
WDRSN |
10 |
Sponsor decision (specify) |
WDRSN |
11 |
Primary Care Physician decision (specify |
WDRSN |
12 |
Informant / Caregiver decision (specify) |
WDRSN |
13 |
Institutionalized |
WDRSN |
14 |
Inability to continue giving consent |
WDRSN |
15 |
Other (specify) |
WDRSN |
20 |
Subject transitioning to a new cohort |
Missing Columns
ITM_NAME |
DSCR_1.0 |
|---|---|
COMPLT |
Did the subject complete the study? |
WDDT |
Withdrawal date |
WDRSN |
Reason for withdrawal |
WDRSNCM |
Withdrawal comment |
Details
The CONCL table captures the Conclusion of Study Particpation form. All participants in the PPMI 2.0 Study use this form on an as-needed basis. Early Imaging Sub-Study participants use the AVCONCL CRF.
WDRSN
The possible values for this variable have been harmonized to account for versions of the form that were used both in the original and extended phases of the PPMI study. “Other” in the extended version was recoded from 8 to 20 and codes 9-15 were added to account for possible values in the original version of the form. Codes 4, 9, 11, and 13 from the original version are not accounted for as they were never used in that phase.