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Randomised controlled trial of the effectiveness of Mental Health Guru, an internet-based workplace induction program for depression and anxiety.

A randomised controlled trial evaluating the effect of Mental Health Guru, an internet-based workplace mental health induction program, on mental health literacy, stigma and help-seeking in a workplace population.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613001083785
Enrollment
880
Registered
2013-09-26
Start date
2014-07-11
Completion date
2014-11-12
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study aims to test whether an internet-based workplace mental health induction program is effective in increasing mental health literacy, decreasing stigma and improving help-seeking attitudes and intentions for depression and anxiety when compared to a wait-list control group.

Interventions

This study will test the effectiveness of a brief, internet-based, workplace mental health program- Mental Health Guru - using a randomised controlled trial design. The Mental Health Guru program is an online educational program currently comprising two modules: 1) depression and 2) generalised anxiety disorder each of which comprises information about mental illness and the myths associated with it, personalised feedback and consumer videos. Participants randomly allocated to the intervention

This study will test the effectiveness of a brief, internet-based, workplace mental health program- Mental Health Guru - using a randomised controlled trial design. The Mental Health Guru program is an online educational program currently comprising two modules: 1) depression and 2) generalised anxiety disorder each of which comprises information about mental illness and the myths associated with it, personalised feedback and consumer videos. Participants randomly allocated to the intervention condition will be asked to complete one module per week, with each module requiring approximately 30 minutes to complete. The program can be completed via home or work computers. Program usage data will be captured from the technology systems including program module access, number of site visits and an estimate of length of exposure derived from log analysis.

Sponsors

Professor Kathleen Griffiths
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants must be employed by an organisation that has provided written consent to participate in the trial.

Exclusion criteria

No exclusion criteria

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026