None listed
Conditions
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 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
Study design
Eligibility
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.