跳至主要内容
临床试验/NCT00741650
NCT00741650已完成2 期

Ibedrift- Health Related Coping. A Randomized Controlled Trial Comparing a Worksite Educational Intervention With or Without Referral to Treatment as Usual.

NORCE Norwegian Research Centre AS2 个研究点 分布在 1 个国家目标入组 2,097 人开始时间: 2008年9月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
2,097
试验地点
2
主要终点
Sick Leave

研究概览

简要总结

A randomized controlled trial comparing a new approach to musculoskeletal pain consisting of education and peer involvement to treatment as usual. All local government employees in 1-3 Norwegian municipalities will be invited to participate.

详细描述

The purpose of the study is to systematically test a new treatment method for musculoskeletal pain in Norway. The intervention focuses on attempting to treat musculoskeletal pain outside the traditional medical system as much as possible, to avoid the establishment of a patient identity and passive patient behavior. In addition, participants are given reasons to stay active, and not advice to stay active.

Ibedrift is a randomized controlled trial with the aim of studying the effect of a new treatment regime for musculoskeletal pain, focusing on didactic information about low back pain with peer support. Those participants not in the control group will have the option of contacting a peer advisor, a non health professional trained by the iBedrift crew to give information about back pain and reasons to stay active. For those who have not recovered within a short period of time, and who are randomized to full treatment, the peer advisor can send them directly to health personnel for a brief intervention consisting of a medical examination with screening for conditions that need treatment, counseling and education.

The intervention was done in 2 Norwegian municipalities for all local government employees. Randomization was done at the level of working units (schools, offices etc) which allows for more message containment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All employees above 18 years

排除标准

  • Known congenital musculoskeletal disease
  • Cauda equina syndrome

结局指标

主要结局

Sick Leave

时间窗: 1 year and 2 year after start of intervention

次要结局

  • Low Back pain(1 year and 2 years after intervention)
  • Subjective Health complaints(1 year and 2 years after intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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