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Trial of an at home screening program for investigation of obstructive sleep apnoea in rail safety workers

Trial of an at home screening program for investigation of obstructive sleep apnoea in rail safety workers

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611000185965
Acronym
nil
Enrollment
100
Registered
2011-02-16
Start date
2011-04-01
Completion date
Unknown
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

The aim of this pilot study is to assess whether or not objective health criteria (inclusion criteria), coupled with a portable home monitor (ApneaLink) could be a more reliable and valid method of screening for obstructive sleep apnoea in Rail Safety Workers, when compared with the current self reported Epworth Sleepiness Scale.

Interventions

Participants who meet the inclusion criteria will undertake an at home sleep assessment via a portable home monitoring device to screen for obstructive sleep apnoea. Participants will be given instruction on how to operate and administer this device by an occupational health nurse during their routine medical assessments. The device is about the size of a mobile telephone. Participants will take the device home for use on the night of their periodic Rail Safety assessment. The device (the "

Participants who meet the inclusion criteria will undertake an at home sleep assessment via a portable home monitoring device to screen for obstructive sleep apnoea. Participants will be given instruction on how to operate and administer this device by an occupational health nurse during their routine medical assessments. The device is about the size of a mobile telephone. Participants will take the device home for use on the night of their periodic Rail Safety assessment. The device (the "ApneaLink") is a portable battery powered 3 channel unit that measures: 1. nasal flow (via nasal cannulae) 2. oxygen saturation (via finger sensor) 3. chest expansion (via a chest strap) Participants will undertake the study in their own home/bed, and will be instructed to attach the leads and turn the device on around 15-20 minutes before sleep. They will then be asked to turn the unit off when they wake the next morning, after preferably at least 6 hours of sleep time in between. The above parameters are recorded via the unit, and data will be extracted the next day once the unit is returned to study centre. The data will then be extracted and analysed to assess whether or not there are any periods of apnoea (cessation of breathing) or hyponoea (reduced breathing) during sleep. A sleep physician will then interpret the data and give opinion as to whether or not there are any characteristics of obstructive sleep apnoea.

Sponsors

Medibank Health Solutions
Lead SponsorCommercial sector/Industry

Eligibility

Sex/Gender
Male
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Railcorp Safety Critical Workers males body mass index >35 neck circumference >43 cm with: known hypertension or systolic blood pressure >150mmHg or impaired glucose tolerance or known diabetes mellitus

Exclusion criteria

- non railcorp safety critical workers - known obstructive sleep apnoea or other sleep disordered breathing

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026