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The Computer Automated Pause Software (CAPS) study, randomised controlled trial in the effectiveness of pause software in VDU workers.

The Computer Automated Pause Software (CAPS) study, randomised controlled trial in the effectiveness of pause software in VDU workers for prevention of work related upper extremity complaints.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25225
Enrollment
600
Registered
2005-06-24
Start date
2005-08-22
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

None listed

Interventions

The intervention group will have break software at their disposal in an active way: they will know how to set up and use the software and will have background information on the possible benefits of t

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Workers with at least 4 hours of VDU work per day. In light of the prevalence of complaints, a maximum of 40% of the included workers will have (or will have had) RSI complaints.

Exclusion criteria

Exclusion criteria: All other than the inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Main outcomes are prevalence and incidence of RSI risk factors and complaints. A worker will be defined as a RSI case in case symptoms are present on at least 4 days during at least 1 week in the last 12 months. Symptoms have to be present in one or more of the upper extremity body regions: neck, upper back, shoulder, elbow, forearm, wrist and/or hand (SALTSA definition). Duration of computer use will be registered with WorkPace registration software. Complaints will be measured with the QuickDASH questionnaire. Pain and complaints in the previous 24 hours will be measured with a Visual Analogue Scale. The average pain intensity in will be evaluated by the worker on an 11-pointnumerical scale ranging from 0 (no pain) to 10 (as much as can be imagined).

Secondary

MeasureTime frame
Data on costs will be gathered from several sources. Data on sick leave will be gathered from the companies registration Direct costs (visits to the general practitioner etc) due to upper limb musculoskeletal disorders will be gathered by questionnaire. Data on productivity will be collected by registering the amount of processed claims.

Contacts

Public ContactEline M. Meijer

Academic Medical Center (AMC), Coronel Institute for occupational and Environmental Health, P.O. Box 22660

e.m.meijer@amc.uva.nl+31 (0)20 5662799

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)