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Evaluate the Usefulness of Mental Health e-Learning

Randomized Trial to Evaluate the Usefulness of Mental Health e-Learning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06393322
Enrollment
125
Registered
2024-05-01
Start date
2024-08-06
Completion date
2025-06-30
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression

Keywords

Depression, Mental Health, Mental Health Literacy, e-Learning, Knowledge, Stigma, Randomized Controlled Trial

Brief 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.

Interventions

OTHERDepression 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. 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.

OTHERDepression 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. 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.

OTHERAnxiety e-Learning A

Participants in Anxiety e-Learning A will be provided e-learning about anxiety, consisting of following components: 1. One multimedia e-learning lesson on anxiety; 2. A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson.

OTHERAnxiety e-Learning B

Participants in Anxiety e-Learning B will be provided e-learning about anxiety, consisting of following components: 1. One multimedia e-learning lesson on anxiety; 2. A series of 4 'micro-learning' emails (2 emails/week) with small segments of content to reinforce the material from the lesson.

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in the Depression Literacy Questionnaire0, 2, 4 weeksThe 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.
Change from baseline in the Anxiety Literacy Questionnaire0, 2, 4 weeksThe 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.

Secondary

MeasureTime frameDescription
Change from baseline in the Depression Stigma Scale0, 2, 4 weeksThe 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.
Change from baseline in the Generalized Anxiety Stigma Scale0, 2, 4 weeksThe 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.
Participant satisfaction2 weeksA custom satisfaction questionnaire data adapted from the Information Assessment Method For All (IAM4all) will be collected and saved to assess satisfaction with the intervention.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026