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Psychometric / Validation Study

This study is enrolling participants by invitation only.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01717365
First Posted: October 30, 2012
Last Update Posted: April 25, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Patricia Bowyer, Texas Woman's University
  Purpose
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.

Condition
To Determine the Psychometric Properties of the Short Child Occupational Profile (SCOPE) and Validate the SCOPE.

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: SCOPE: A Psychometric Study

Further study details as provided by Patricia Bowyer, Texas Woman's University:

Primary Outcome Measures:
  • To determine the psychometric properties of the Short Child Occupational Profile Validate SCOPE [ Time Frame: Up to 3 years- May 2019 - Anticipated ]
    To determine the psychometric properties of the Short Child Occupational Profile (SCOPE) and validate the SCOPE.


Estimated Enrollment: 500
Study Start Date: March 2008
Estimated Study Completion Date: August 2018
Estimated Primary Completion Date: August 2018 (Final data collection date for primary outcome measure)
Groups/Cohorts
OTs
Occupational therapists

Detailed 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.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   up to 21 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
The subjects from the data shared by the therapists are from the ages of 0-21, both male and female, and of any ethnicity.
Criteria

Inclusion Criteria:

Subjects receiving therapy from participating therapists.

Exclusion Criteria:

Age over 21.

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01717365


Locations
United States, Texas
Texas Woman's University
Houston, Texas, United States, 77030
Sponsors and Collaborators
Texas Woman's University
  More Information

Responsible Party: Patricia Bowyer, Patricia Bowyer, EdD, , MS, OTR, FAOTA, Texas Woman's University
ClinicalTrials.gov Identifier: NCT01717365     History of Changes
Other Study ID Numbers: 15007
First Submitted: October 26, 2012
First Posted: October 30, 2012
Last Update Posted: April 25, 2016
Last Verified: April 2016

Keywords provided by Patricia Bowyer, Texas Woman's University:
SCOPE


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