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dc.contributor.authorFimland, Marius Steiro
dc.contributor.authorVasseljen, Ottar
dc.contributor.authorGismervik, Sigmund Østgård
dc.contributor.authorRise, Marit By
dc.contributor.authorHalsteinli, Vidar
dc.contributor.authorJacobsen, Henrik Børsting
dc.contributor.authorBorchgrevink, Petter Chr.
dc.contributor.authorTenggren, Hanne
dc.contributor.authorJohnsen, Roar
dc.date.accessioned2015-09-11T12:43:45Z
dc.date.accessioned2015-09-28T14:26:10Z
dc.date.available2015-09-11T12:43:45Z
dc.date.available2015-09-28T14:26:10Z
dc.date.issued2014
dc.identifier.citationBMC Public Health 2014, 14(1)nb_NO
dc.identifier.issn1471-2458
dc.identifier.urihttp://hdl.handle.net/11250/302337
dc.description.abstractBackground: Long-term sick leave has considerably negative impact on the individual and society. Hence, the need to identify effective occupational rehabilitation programs is pressing. In Norway, group based occupational rehabilitation programs merging patients with different diagnoses have existed for many years, but no rigorous evaluation has been performed. The described randomized controlled trial aims primarily to compare two structured multicomponent inpatient rehabilitation programs, differing in length and content, with a comparative cognitive intervention. Secondarily the two inpatient programs will be compared with each other, and with a usual care reference group. Methods/design: The study is designed as a randomized controlled trial with parallel groups. The Social Security Office performs monthly extractions of sick listed individuals aged 18–60 years, on sick leave 2–12 months, with sick leave status 50% - 100% due to musculoskeletal, mental or unspecific disorders. Sick-listed persons are randomized twice: 1) to receive one of two invitations to participate in the study or not receive an invitation, where the latter “untouched” control group will be monitored for future sick leave in the National Social Security Register, and 2) after inclusion, to a Long or Short inpatient multicomponent rehabilitation program (depending on which invitation was sent) or an outpatient cognitive behavioral therapy group comparative program. The Long program consists of 3 ½ weeks with full rehabilitation days. The Short program consists of 4 + 4 full days, separated by two weeks, in which a workplace visit will be performed if desirable. Three areas of rehabilitation are targeted: mental training, physical training and work-related problem solving. The primary outcome is number of sick leave days. Secondary outcomes include time until full sustainable return to work, health related quality of life, health related behavior, functional status, somatic and mental health, and perceptions of work. In addition, health economic evaluation will be performed, and the implementation of the interventions, expectations and experiences of users and service providers will be investigated with different qualitative methods.nb_NO
dc.language.isoengnb_NO
dc.publisherBioMed Centralnb_NO
dc.titleOccupational rehabilitation programs for musculoskeletal pain and common mental health disorders: Study protocol of a randomized controlled trialnb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-09-11T12:43:45Z
dc.source.volume14nb_NO
dc.source.journalBMC Public Healthnb_NO
dc.source.issue1nb_NO
dc.identifier.doi10.1186/1471-2458-14-368
dc.identifier.cristin1170912
dc.description.localcode© 2014 Fimland et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 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.nb_NO


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