- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05123794
Shortened Depression Assessment Study
Using the Long to Short Approach to Develop Rapid Depressions Scales
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Ontario
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Toronto, Ontario, Canada
- University of Toronto
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18 and above
- Must be able to read English
- Must have access to the Internet worldwide
Exclusion Criteria:
- Children aged 17 and under
- Persons who cannot read English
- Persons that do not have access to Internet
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rapid Depression Assessment Tool based on Depression Anxiety Stress Scale 42
Time Frame: All participants completed the same assessments, which took 10-15 minutes
|
Participants filled out an online questionnaire about their demographic information (age, sex, and ethnicity) and all 42 items from the Depression Anxiety Stress Scale (DASS-42). Each item consists of a 4-point Likert scale from 0 to 3, where 0 means "Did not apply to me at all" and 3 means "Applied to me very much, or most of the time". The depression score is the sum of scores for the items in the depression sub-scale. A higher score indicates a more severe level of depression symptoms. Machine learning techniques were used to develop a shortened assessment (Rapid Depression Assessment Tool) using demographics and 5 DASS-42 items from the original questionnaire, to predict severity levels of depression indicated by DASS-42. The assessment tool calculates the likelihood of moderate depression symptoms and severe depression symptoms given the responses from each item (ranging from 0 to 3). The data was collected and aggregated through a public website. |
All participants completed the same assessments, which took 10-15 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Kang Lee, University of Toronto
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0032755
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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