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The efficacy of sleep education and wrist-activity monitor smartphone apps on improving sleep and performance in shiftworkers.

The efficacy of sleep education and wrist-activity monitors that provide daily feedback on sleep, on the sleep quality, quantity and cognitive performance of shiftworkers.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001774112
Acronym
FRMT (Fatigue Risk Management Trial)
Enrollment
88
Registered
2019-12-13
Start date
2020-02-17
Completion date
2020-02-25
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

A multi-armed randomised control trial to assess the effectiveness of sleep education and wrist-activity monitors that provide daily feedback on sleep . These interventions were selected as they are frequently used by shiftwork organisations as part of a systematic approach to manage fatigue risk. However, the effectiveness of these interventions is somewhat unknown. An assessment of sleep quality, quantity, and cognitive performance will follow these interventions using both subjective and objective measures.

Interventions

This study involves participants who undertake shiftwork for a Western Australian mining company. Participants are assigned to one of three intervention groups. Intervention group 1 will attend a 2-hour face to face group sleep education session; intervention group 2 will receive daily feedback on sleep via a wrist-activity monitor mobile app; and intervention group 3 will attend a 2-hour face to face group sleep education session and receive daily feedback on sleep via a wrist-activity monitor

This study involves participants who undertake shiftwork for a Western Australian mining company. Participants are assigned to one of three intervention groups. Intervention group 1 will attend a 2-hour face to face group sleep education session; intervention group 2 will receive daily feedback on sleep via a wrist-activity monitor mobile app; and intervention group 3 will attend a 2-hour face to face group sleep education session and receive daily feedback on sleep via a wrist-activity monitor mobile app. The sleep education sessions will be delivered onsite by the researcher who has worked in the area of fatigue risk management for the past 7 years and holds a Post Graduate Diploma in Health and Safety, a Graduate Certificate in Public Health and a Bachelor of Science in Health Promotion. Sleep Education Sessions - Interactive group sessions that include powerpoint presentation, videos, and discussion that address the following: • What fatigue is and the importance of sleep in maintaining good health. • The science of sleep, our biological clock and circadian rhythms. • Common sleep disorders. • Sleep deprivation and the dangers associated with micro-sleeps. • How to recognise the signs of fatigue in yourself and others. • Lifestyle and environmental factors that contribute to good quality and quantity sleep. • Strategies to prepare for shift work. • Strategies to manage fatigue and increase alertness during your shift. Wrist-activity monitors - participants will wear a wrist-activity monitor 24 hrs a day (unless required to remove for safety reasons whilst at work) for the duration of 2 roster cycles (approx 42 days): pre-intervention, 21-days and post-intervention 21-day roster cycle. The intervention group with access to the mobile app will receive daily info on their sleep quality, quantity and performance ie: sleep duration, sleep fragmentation, alertness levels. This intervention group will be required to sync their data daily with the mobile app allowing the researcher to monitor adherence to the intervention through a overall web app. The researcher will send text message reminders if participants aren't syncing their data.

Sponsors

Gemma Maisey
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Factorial
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject)

Eligibility

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

Inclusion criteria

Shiftworkers from the participating organisation who meet the below criteria will be eligible to participate in this research. 1, Participants should be available for the duration of the study with no annual leave booked. 2. Participants should be undertaking the identified roster pattern that includes working days and nights for the duration of the study. 3. Participants shift start and finish times should be those identified for the study. 4. Participants must have access to a smartphone or tablet device to download the Fatigue Science mobile app and receive daily sleep feedback (required if assigned to intervention groups 2 and 3).

Exclusion criteria

There are no exclusion criteria for this study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026