Your browser doesn't support javascript.
loading
Protocol for the Individual Placement and Support (IPS) in Pain Trial: A randomized controlled trial investigating the effectiveness of IPS for patients with chronic pain.
Linnemørken, Lene Therese B; Sveinsdottir, Vigdis; Knutzen, Thomas; Rødevand, Linn; Hernæs, Kjersti Helene; Reme, Silje Endresen.
Afiliação
  • Linnemørken LTB; Department of Pain Management and Research, Oslo University Hospital, Oslo, Norway.
  • Sveinsdottir V; Uni Research Health, Uni Research, Bergen, Norway.
  • Knutzen T; Department of Pain Management and Research, Oslo University Hospital, Oslo, Norway.
  • Rødevand L; Department of Pain Management and Research, Oslo University Hospital, Oslo, Norway.
  • Hernæs KH; NORMENT, KG Jebsen Centre for Psychosis Research, Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.
  • Reme SE; Oslo University Hospital, Oslo, Norway.
BMC Musculoskelet Disord ; 19(1): 47, 2018 02 13.
Article em En | MEDLINE | ID: mdl-29433493
ABSTRACT

BACKGROUND:

Work disability involves large costs to the society as well as to the individual. Work disability is common among people with chronic pain conditions, yet few effective interventions exist. Individual Placement and Support (IPS) is an evidence-based work rehabilitation model originally developed to help people with severe mental illness obtain and maintain employment. The effectiveness of IPS for patients with severe mental illness is well documented, but the model has never before been tested for patients with chronic pain. METHODS/

DESIGN:

The aim of the IPS in Pain trial is to investigate the effectiveness of IPS as an integrated part of the interdisciplinary treatment for patients with chronic pain in a hospital outpatient clinic. The study is a randomized controlled trial comparing pain treatment with integrated IPS to treatment as usual in unemployed patients suffering from various chronic pain conditions. The primary outcome of the study is labor market participation during 12 months after enrollment, and secondary outcomes include physical and mental health and well-being, collected at baseline, 6, and 12 months. Finally, there will be an additional long-term follow-up for the primary outcome, which will be collected through a brief phone interview at 24 months.

DISCUSSION:

The IPS in Pain trial will be the first report of the effectiveness of the IPS model of supported employment applied in an outpatient setting for chronic pain patients. It will thus provide important information about the effectiveness of repurposing IPS to a new patient group in great need of job support. TRIAL REGISTRATION Clinicaltrials.gov NCT02697656 . Registered January 15th, 2016.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reabilitação Vocacional / Medição da Dor / Readaptação ao Emprego / Dor Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reabilitação Vocacional / Medição da Dor / Readaptação ao Emprego / Dor Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article