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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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28 April 2013 |
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Main ID: |
NTR1117 |
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Date of registration:
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13/09/2007 |
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Primary sponsor: |
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Public title:
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Effectiveness of the RSI QuickScan.
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Scientific title:
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Effectiveness of the RSI QuickScan in relation to primary and secondary prevention of RSI. - Effectiveness of the RSI QuickScan in relation to primary and secondary prevention of RSI. |
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Date of first enrolment:
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1/4/2004 |
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Target sample size:
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1000 |
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Recruitment status: |
complete |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1117 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: Single; Control: Active; Group: Parallel; Type: 2 or more arms, randomized
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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Erwin
Speklé |
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Address:
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Faculty of Human Movement Sciences
VU University Amsterdam
Van der Boechorststraat 9
1081 BT
Amsterdam
The Netherlands |
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Telephone:
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+31 20 598 8451 |
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Email:
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e.spekle@fbw.vu.nl |
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Affiliation:
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Name:
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Erwin
Speklé |
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Address:
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Faculty of Human Movement Sciences
VU University Amsterdam
Van der Boechorststraat 9
1081 BT
Amsterdam
The Netherlands |
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Telephone:
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+31 20 598 8451 |
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Email:
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e.spekle@fbw.vu.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. All workers with 2 hours or more computerwork per day;
2. Workers without- and with arm, neck and shoulder symptoms are included in the trial.
Exclusion criteria: Workers with less than 2 hours computer work per day or those who did not give their consent to particpate in the investigation.
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Repetitive Strain Injury (RSI) , Upper-extremity disorders (UED)
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Intervention(s)
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RSI QuickScan (questionnaire with feedback) and preventive RSI interventions based on questionnaire results.
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Primary Outcome(s)
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Occurrence of risk factors, RSI complaints and absenteeism is assessed using the RSI QuickScan (web-based questionnaire) at baseline and 6 and 12 month follow-up.
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Secondary ID(s)
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WC2004-030
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Source(s) of Monetary Support
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ZON-MW, The Netherlands Organization for Health Research and Development, ArboUnie
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