Return to Work After Potential Severe Injury

NCT02602405 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1741

Last updated 2017-12-21

No results posted yet for this study

Summary

In Norway an estimated 10 % of the population is injured annually. Of these 36.000 sustain permanent functional impairment, 1.200 receive disability pension, and approximately 2.500 die because of their injuries. Mortality is the most common variable measuring trauma outcome. However, measuring only trauma mortality may be looking merely at the tip of the iceberg. For every trauma death, there are ten-folds suffering long term functional impairment. Mortality is therefore a too crude variable to describe the impact of injuries - both for the individual trauma patient and for society as a whole. There is a need for variables describing long-term outcomes on a functional level. The aim of this study is to use the rate of return to work and education as an alternative outcome measure. The ability of returning to work after injury is a central indicator of individual functional outcome, combining both physical and mental skills in performing complex and compound tasks. Previous studies on return to work after injury are limited by a combination of short follow-up times, the use of patient reported outcomes and having mainly been focusing on only severely injured patients (ISS \> 15). This a population-based study including all patients in working age (16 - 65 years) received by a trauma team in any of the eight hospitals within the region of Central Norway in the time period from June 1st,2007 to May 30th, 2010. Already collected trauma registry data will be linked with national register data on sickness and disability benefits, employment and education.

Conditions

  • Multiple Trauma

Sponsors & Collaborators

  • St. Olavs Hospital

    collaborator OTHER
  • Statistics Norway

    collaborator INDUSTRY
  • Namsos Hospital

    collaborator OTHER
  • Helse Nord-Trøndelag HF

    collaborator OTHER
  • Alesund Hospital

    collaborator OTHER
  • Molde Hospital

    collaborator OTHER
  • Kristiansund Hospital

    collaborator OTHER
  • Norwegian University of Science and Technology

    lead OTHER

Principal Investigators

  • Pål Klepstad, md prof · Norwegian University of Science and Technology

Eligibility

Min Age
16 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2016-08-31
Completion
2016-08-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02602405 on ClinicalTrials.gov