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Effectiveness of a lumbo-pelvic monitor and feedback device to change postural behaviour in healthcare workers

The effectiveness of a lumbopelvic monitor and feedback device to change postural behaviour in healthcare workers with or without low back pain: a clustered randomized controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000449437
Acronym
ELF Study
Enrollment
130
Registered
2016-04-07
Start date
2016-04-28
Completion date
2017-04-01
Last updated
2023-07-18

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

Conditions

None listed

Brief summary

The study will assess whether a postural monitor and feedback device can help workers to prevent hazardous posture at the workplace. It is hypothesized that workers exposed to the feedback intervention will change their postural behaviour and reduce the amount of time spent in flexed posture at the workplace.

Interventions

Postural data will be recorded, and audio-feedback provided through a postural monitor feedback device. This device consists of a tri-axial accelerometer and data recorder, and has the size of a pager. Data will be collected over a 6 week period and then at follow-up time points. During the first and sixth week, baseline and post-intervention measurements will be collected. The intervention period consists of 4 weeks (weeks 2 to 5, inclusive). Arm 1 - Feedback Group (FG) The FG will received p

Postural data will be recorded, and audio-feedback provided through a postural monitor feedback device. This device consists of a tri-axial accelerometer and data recorder, and has the size of a pager. Data will be collected over a 6 week period and then at follow-up time points. During the first and sixth week, baseline and post-intervention measurements will be collected. The intervention period consists of 4 weeks (weeks 2 to 5, inclusive). Arm 1 - Feedback Group (FG) The FG will received postural audio-feedback, whenever the postural threshold is exceeded, during the four weeks of intervention. The field coordinator will be responsible for setting the devices and handing these to healthcare workers at the beginning of every week. Participants will wear the device clipped to their waistband or belt, during working hours, over the working days of each week. To enhance adherence, workers will receive reminders to their mobile phones (if they consent with that), and reminders will be printed and placed at strategic areas of the workplace. Adherence will be assessed as the number of days participants worked with the lumbopelvic monitor and feedback device, and was will be expressed as a percentage of total working days of that specific week.

Sponsors

University of Otago
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Adult healthcare workers, with or without LBP, presently performing their regular work activities, will be included.

Exclusion criteria

Participants who work less than 20 hours/week or are unable to undertake regular work-related activities due to LBP or any other musculoskeletal disorder will be excluded from this study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 27, 2026