Validity of a Test of Functional Cognition in Persons With Acquired Brain Injury
1 other identifier
observational
73
1 country
1
Brief Summary
The purpose of this study is to test the validity of the Weekly Calendar Planning Activity (WCPA), a test of functional cognition in persons with acquired brain injury. We will formally examine the utility, baseline profile and validity of the WCPA with adults ages 21 and above with acquired brain injury for both the WCPA 17 and WCPA 10 versions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2017
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 12, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 5, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
February 5, 2020
CompletedFirst Submitted
Initial submission to the registry
June 22, 2021
CompletedFirst Posted
Study publicly available on registry
June 29, 2021
CompletedJune 29, 2021
June 1, 2021
3.1 years
June 22, 2021
June 22, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
WCPA Percent Accuracy
The Weekly Calendar Planning Activity (WCPA) is a performance-based Cognitive Instrumental activities of daily living (C-IADL) task that requires working memory, planning, shifting, inhibition, and self-monitoring. The WCPA requires the examinee to input a series of 10 appointments, into a mock weekly calendar/schedule while following multiple rules, managing appointment conflicts, ignoring distracting questions by the examiner and keeping track of time. WCPA percent accuracy is the number of appointments entered correctly out of 10.
During hospitalization, approximately one week
Interventions
Eligibility Criteria
Persons with acquired brain injury receiving inpatient occupational therapy
You may qualify if:
- Able to attend for at least 10 minutes
- Able to read and write legibly in English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Weill Cornell Medicine
New York, New York, 10065, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michael O'Dell, MD
Weill Medical College of Cornell University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 22, 2021
First Posted
June 29, 2021
Study Start
January 12, 2017
Primary Completion
February 5, 2020
Study Completion
February 5, 2020
Last Updated
June 29, 2021
Record last verified: 2021-06
Data Sharing
- IPD Sharing
- Will not share