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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06393322
Other study ID # Levinson_AFP
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2, 2024
Est. completion date June 30, 2025

Study information

Verified date April 2024
Source McMaster University
Contact Ayers
Phone 9055259140
Email ayerss@mcmaster.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this proposal, the investigators plan to study the impact of In this proposal, we plan to study the impact of e-learning on mental health literacy and stigma related to anxiety and depression. Participants will be randomized to one of four groups - Depression e-Learning A, Depression e-Learning B, Anxiety e-Learning A, and Anxiety e-Learning B. All participants will be given access to all e-learning at the conclusion of the study.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 125
Est. completion date June 30, 2025
Est. primary completion date September 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Depression e-Learning A
Participants in Depression e-Learning A will be provided e-learning about depression, consisting of following components: One multimedia e-learning lesson on depression; A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson. 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.
Depression e-Learning B
Participants in Depression e-Learning B will be provided e-learning about depression, consisting of following components: One multimedia e-learning lesson on depression; A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson. 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.
Anxiety e-Learning A
Participants in Anxiety e-Learning A will be provided e-learning about anxiety, consisting of following components: One multimedia e-learning lesson on anxiety; A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson.
Anxiety e-Learning B
Participants in Anxiety e-Learning B will be provided e-learning about anxiety, consisting of following components: One multimedia e-learning lesson on anxiety; A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
McMaster University

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in the Depression Literacy Questionnaire 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
Primary Change from baseline in the Anxiety Literacy Questionnaire 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 Change from baseline in the Depression Stigma Scale 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
Secondary Change from baseline in the Generalized Anxiety Stigma Scale 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
Secondary Participant satisfaction 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
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