Psychometric / Validation Study

To Determine the Psychometric Properties of the Short Child Occupational Profile Clinical Trial

Official title:

SCOPE: A Psychometric Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01717365
• Other study ID #: 15007
• Status: Completed
• Phase: N/A
• First received: October 26, 2012
• Last updated: October 11, 2017

Study information

• Verified date: October 2017
• Source: Texas Woman's University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 499
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 21 Years

Eligibility

Inclusion Criteria:

Subjects receiving therapy from participating therapists.

Exclusion Criteria:

Age over 21.

Related Conditions & MeSH terms

• To Determine the Psychometric Properties of the Short Child Occupational Profile

Locations

Country	Name	City	State
United States	Texas Woman's University	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Texas Woman's University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine the psychometric properties of the Short Child Occupational Profile Validate SCOPE	To determine the psychometric properties of the Short Child Occupational Profile (SCOPE) and validate the SCOPE.	36 months