A Prospective Chart Review to Validate the WFIRS (Weiss Functional Impairment Rating Scale)
Psychometric Validation of the Weiss Functional Impairment Rating Scale and the Weiss Symptom Record in Patients With Attention-Deficit Hyperactivity Disorder
1 other identifier
observational
220
1 country
1
Brief Summary
The purpose of the study is to evaluate the psychometric validation of the Weiss Functional Impairment Rating Scale and the Weiss Symptom Record. It is hypothesized that the Weiss Functional Impairment Rating Scale has strong psychometric properties and good convergent validity with other measures of functioning and discriminant validity from symptoms and quality of life.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2006
Longer than P75 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
July 1, 2006
CompletedFirst Submitted
Initial submission to the registry
April 20, 2009
CompletedFirst Posted
Study publicly available on registry
April 22, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2011
CompletedJune 20, 2011
June 1, 2011
4.8 years
April 20, 2009
June 17, 2011
Conditions
Keywords
Eligibility Criteria
People with ADHD from 7 years of age
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of British Columbialead
- Eli Lilly and Companycollaborator
- Purdue Pharma LPcollaborator
- Shirecollaborator
Study Sites (1)
Provincial ADHD Program, BC Children's & Women's Health Centre
Vancouver, British Columbia, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Margaret D. Weiss, MD, Ph.D
University of British Columbia
- STUDY DIRECTOR
Chistopher Gibbins, MD
BC Children's & Women's Hospital, Vancouver
- STUDY DIRECTOR
Grant Iverson, MD
University of British Columbia
- STUDY DIRECTOR
Brian Brooks, MD
BC Children's & Women's Hospital, Vancouver
- STUDY DIRECTOR
Li Ying Lu, MD
BC Children's & Women's Hospital, Vancouver
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 20, 2009
First Posted
April 22, 2009
Study Start
July 1, 2006
Primary Completion
April 1, 2011
Study Completion
April 1, 2011
Last Updated
June 20, 2011
Record last verified: 2011-06