Psychometric / Validation Study
Data for the study will be collected from therapist across the world. The therapists will share data they have already compiled from their caseload. Data will be stripped of all personal identifiers and personal health information. The TWU SCOPE research team has no contact with clients whose assessment data is being shared for secondary analysis or clinical data repository. For educational and training purposes clients can be videotaped by the therapist who will obtain consent and/or assent from the client. Not every client will be videotaped. The subjects from the data shared by the therapists are from the ages of 0-21, both male and female, and of any ethnicity. The total amount of data collected from all participating therapists will be 500 pieces.
To Determine the Psychometric Properties of the Short Child Occupational Profile (SCOPE) and Validate the SCOPE.
|Study Design:||Observational Model: Cohort
Time Perspective: Retrospective
|Official Title:||SCOPE: A Psychometric Study|
- To determine the psychometric properties of the Short Child Occupational Profile Validate SCOPE [ Time Frame: Up to 3 years- May 2013 - Anticipated ] [ Designated as safety issue: No ]To determine the psychometric properties of the Short Child Occupational Profile (SCOPE) and validate the SCOPE.
|Study Start Date:||March 2008|
|Estimated Primary Completion Date:||June 2014 (Final data collection date for primary outcome measure)|
Therapists will be recruited by a TWU SCOPE research team member via email. Therapists who wish to participate will send a data sharing letter to the PI of the study. Once the TWU SCOPE research team has received the data sharing letter, a clinical data packet will then be distributed to the therapist through the U.S. mail or an email will be sent containing a web address link to http://www.myweb.twu.edu/~ttioseco for access to the clinical data packet via the internet. Those therapists who collect ten pieces or more of de-identified data and send them to the TWU SCOPE research team will receive an incentive in the form of a gift card.
Flow Chart of Research Study Process Collaborators (share new de-identified data) → databank (new de-identified data input) → data analysis (analysis of new and old de-identified data) → publication/presentation
No risks are involved because data collected is without any personal identifiers.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01717365
|United States, Texas|
|Texas Woman's University||Recruiting|
|Houston, Texas, United States, 77030|
|Contact: Patricia Bowyer, EdD, OTR, BCN, FAOTA (713) 794-2128 firstname.lastname@example.org|
|Principal Investigator: Patricia Bowyer, EdD OTR BCN|