- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06393322
Evaluate the Usefulness of Mental Health e-Learning
Randomized Trial to Evaluate the Usefulness of Mental Health e-Learning
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, L8S4L8
- McMaster University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Live in Canada
- 45 years of age and over
- Good command of the English language
- Access to email and high speed internet
- Comfortable using email and internet
Exclusion Criteria:
- Lives outside of Canada
- Not 45 years of age or over
- Does not speak English,
- Does not have access to email or high speed internet
- Is not comfortable using email of internet
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Depression e-Learning A
|
Participants in Depression e-Learning A will be provided e-learning about depression, consisting of following components:
1. One multimedia e-learning lesson on depression; 2. A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson. |
|
Experimental: Anxiety e-Learning A
|
Participants in Anxiety e-Learning A will be provided e-learning about anxiety, consisting of following components:
|
|
Experimental: Depression e-Learning B
|
Participants in Depression e-Learning B will be provided e-learning about depression, consisting of following components:
1. One multimedia e-learning lesson on depression; 2. A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson. |
|
Experimental: Anxiety e-Learning B
|
Participants in Anxiety e-Learning B will be provided e-learning about anxiety, consisting of following components:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in the Depression Literacy Questionnaire
Time Frame: 0, 2, 4 weeks
|
The Depression Literacy Questionnaire assesses mental health literacy specific to depression.
The questionnaire consists of 22 items which are true or false.
Respondents can answer each item with one of three options - true, false, or I don't know.
Each correct response receives one point.
Higher scores indicate higher depression literacy.
|
0, 2, 4 weeks
|
|
Change from baseline in the Anxiety Literacy Questionnaire
Time Frame: 0, 2, 4 weeks
|
The Anxiety Literacy Questionnaire assesses mental health literacy specific to anxiety.
The questionnaire consists of 22 items which are true or false.
Respondents can answer each item with one of three options - true, false, or I don't know.
Each correct response receives one point.
Higher scores indicate higher depression literacy.
|
0, 2, 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in the Depression Stigma Scale
Time Frame: 0, 2, 4 weeks
|
The Depression Stigma Scale is a 9-item assessment designed to measure stigma associated with depression with two subscales: personal and perceived.
The Personal Stigma Subscale measures stigma in the respondents' own attitudes towards depression by asking them to indicate how strongly they personally agree with nine statements about depression.
The Perceived Stigma Subscale measures the respondent's perception about the attitudes of others towards depression by asking them to indicate what they think most other people believe about the same nine statements.
Responses to each item are measured on a five-point scale (ranging from zero 'strongly disagree' to four 'strongly agree').
Higher scores indicate higher levels of depression stigma.
|
0, 2, 4 weeks
|
|
Change from baseline in the Generalized Anxiety Stigma Scale
Time Frame: 0, 2, 4 weeks
|
The Generalised Anxiety Stigma Scale is analogous, but designed to measure stigma associated with anxiety disorders.
It has two subscales: personal and perceived.
The Personal Stigma Subscale measures stigma in the respondents' own attitudes towards anxiety disorders by asking them to indicate how strongly they personally agree with 10 statements about anxiety disorders.
The Perceived Stigma Subscale measures the respondent's perception about the attitudes of others towards anxiety disorders by asking them to indicate what they think most other people believe about the same 10 statements.
Responses to each item are measured on a five-point scale (ranging from zero 'strongly disagree' to four 'strongly agree').
Higher scores indicate higher levels of anxiety stigma.
|
0, 2, 4 weeks
|
|
Participant satisfaction
Time Frame: 2 weeks
|
A custom satisfaction questionnaire data adapted from the Information Assessment Method For All (IAM4all) will be collected and saved to assess satisfaction with the intervention.
|
2 weeks
|
Collaborators and Investigators
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Levinson_AFP
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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