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Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial
BACKGROUND: Workers without a permanent employment contract represent a vulnerable group within the working population. Mental disorders are a major cause of sickness absence within this group. Common mental disorders are stress-related, depressive and anxiety disorders. To date, little attention ha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061521/ https://www.ncbi.nlm.nih.gov/pubmed/24919561 http://dx.doi.org/10.1186/1471-2458-14-594 |
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author | Lammerts, Lieke Vermeulen, Sylvia J Schaafsma, Frederieke G van Mechelen, Willem Anema, Johannes R |
author_facet | Lammerts, Lieke Vermeulen, Sylvia J Schaafsma, Frederieke G van Mechelen, Willem Anema, Johannes R |
author_sort | Lammerts, Lieke |
collection | PubMed |
description | BACKGROUND: Workers without a permanent employment contract represent a vulnerable group within the working population. Mental disorders are a major cause of sickness absence within this group. Common mental disorders are stress-related, depressive and anxiety disorders. To date, little attention has been paid to effective return to work interventions for this type of sick-listed workers. Therefore, a participatory supportive return to work program has been developed. It combines elements of a participatory return to work program, integrated care and direct placement in a competitive job. The objective of this paper is to describe the design of a randomised controlled trial to evaluate the cost-effectiveness of this program compared to care as usual. METHODS/DESIGN: The cost-effectiveness of the participatory supportive return to work program will be examined in a randomised controlled trial with a follow-up of twelve months. The program strongly involves the sick-listed worker in the identification of obstacles for return to work and possible solutions, resulting in a consensus based action plan. This plan will be used as a starting point for the search of suitable competitive employment with support of a rehabilitation agency. During this process the insurance physician of the sick-listed worker contacts other caregivers to promote integrated care. Workers eligible to participate in this study have no permanent employment contract, have applied for a sickness benefit at the Dutch Social Security Agency and are sick-listed between two and fourteen weeks due to mental health problems. The primary outcome measure is the duration until first sustainable return to work in a competitive job. Outcomes are measured at baseline and after three, six, nine and twelve months. DISCUSSION: If the participatory supportive return to work program proves to be cost-effective, the social security system, the sick-listed worker and society as a whole will benefit. A cost-effective return to work program will lead to a reduction of costs related to sickness absence. For the sick-listed worker a cost-effective program results in earlier sustainable return to work, which can be associated with both social and health benefits. TRIAL REGISTRATION: The trial registration number and date is NTR3563, August 7, 2012. |
format | Online Article Text |
id | pubmed-4061521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40615212014-06-19 Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial Lammerts, Lieke Vermeulen, Sylvia J Schaafsma, Frederieke G van Mechelen, Willem Anema, Johannes R BMC Public Health Study Protocol BACKGROUND: Workers without a permanent employment contract represent a vulnerable group within the working population. Mental disorders are a major cause of sickness absence within this group. Common mental disorders are stress-related, depressive and anxiety disorders. To date, little attention has been paid to effective return to work interventions for this type of sick-listed workers. Therefore, a participatory supportive return to work program has been developed. It combines elements of a participatory return to work program, integrated care and direct placement in a competitive job. The objective of this paper is to describe the design of a randomised controlled trial to evaluate the cost-effectiveness of this program compared to care as usual. METHODS/DESIGN: The cost-effectiveness of the participatory supportive return to work program will be examined in a randomised controlled trial with a follow-up of twelve months. The program strongly involves the sick-listed worker in the identification of obstacles for return to work and possible solutions, resulting in a consensus based action plan. This plan will be used as a starting point for the search of suitable competitive employment with support of a rehabilitation agency. During this process the insurance physician of the sick-listed worker contacts other caregivers to promote integrated care. Workers eligible to participate in this study have no permanent employment contract, have applied for a sickness benefit at the Dutch Social Security Agency and are sick-listed between two and fourteen weeks due to mental health problems. The primary outcome measure is the duration until first sustainable return to work in a competitive job. Outcomes are measured at baseline and after three, six, nine and twelve months. DISCUSSION: If the participatory supportive return to work program proves to be cost-effective, the social security system, the sick-listed worker and society as a whole will benefit. A cost-effective return to work program will lead to a reduction of costs related to sickness absence. For the sick-listed worker a cost-effective program results in earlier sustainable return to work, which can be associated with both social and health benefits. TRIAL REGISTRATION: The trial registration number and date is NTR3563, August 7, 2012. BioMed Central 2014-06-12 /pmc/articles/PMC4061521/ /pubmed/24919561 http://dx.doi.org/10.1186/1471-2458-14-594 Text en Copyright © 2014 Lammerts et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Lammerts, Lieke Vermeulen, Sylvia J Schaafsma, Frederieke G van Mechelen, Willem Anema, Johannes R Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title | Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title_full | Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title_fullStr | Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title_full_unstemmed | Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title_short | Return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
title_sort | return to work of workers without a permanent employment contract, sick-listed due to a common mental disorder: design of a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061521/ https://www.ncbi.nlm.nih.gov/pubmed/24919561 http://dx.doi.org/10.1186/1471-2458-14-594 |
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