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uSing Meditation App to Reduce ED occupational sTress - SMART trial

A multi-site, parallel group, two-arm randomised controlled trial to test the effectiveness of using a Meditation App in managing occupational stress among ED staff – Trial Protocol

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001175167
Acronym
SMART trial
Enrollment
148
Registered
2019-08-20
Start date
2019-08-26
Completion date
2019-09-30
Last updated
2021-06-28

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

Conditions

None listed

Brief summary

We hypothesise that introducing a well-designed mindfulness app will reduce staff stress. A multi-site, two-arm randomised controlled trial (RCT) will be conducted at two Queensland hospital EDs. Participants will be encouraged to practice daily, 10 minutes of app (Headspace app®) guided mindfulness-meditation during the four weeks intervention period. The simple intervention has the potential to reduce hospital ED staff stress and improve staff wellbeing. Ultimately it could also improve the bottom-line of operating budgets in Queensland hospitals and most importantly, improve patient care.

Interventions

Participants will be randomised in equal proportions into one of two groups. The experimental group will use a meditation app (Headspace app®) to practice meditation for four weeks. Participants will be encouraged to practice daily, 10 minutes of guided mindfulness-meditation during the four weeks intervention period. The ‘wait to treat’ group will be given access to the app four months later. In order to promote adherence to the intervention, participants will receive regular text message and e

Participants will be randomised in equal proportions into one of two groups. The experimental group will use a meditation app (Headspace app®) to practice meditation for four weeks. Participants will be encouraged to practice daily, 10 minutes of guided mindfulness-meditation during the four weeks intervention period. The ‘wait to treat’ group will be given access to the app four months later. In order to promote adherence to the intervention, participants will receive regular text message and email reminders to use the app during the study period by the principal investigator.

Sponsors

University of Queensland
Lead SponsorUniversity

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 70 Years
Healthy volunteers
Yes

Inclusion criteria

• Either permanent or causal staff in the EDs • Have a daily access to a smartphone with Internet access` • Able to commit to the four weeks intervention period

Exclusion criteria

• Agency staff or external staff • Self-reported with a previous diagnosis of psychiatric disease(s) or severe depression • Have practiced meditation or yoga regularly (practice at least once a week) in the past three months

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026