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临床试验/NCT07793526
NCT07793526招募中不适用

Back on Track: Evaluation of a Computer-Assisted Occupational Reintegration Protocol for Sick-listed Employees With High Risk for Long-Term Sick Leave Due to Musculoskeletal Disorders

Amsterdam UMC, location VUmc1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2025年7月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
140
试验地点
1
主要终点
Time until full RTW

研究概览

简要总结

The objective of the Back on Track study is to evaluate a computer-assisted reintegration protocol for musculoskeletal disorders of a major occupational health service in the Netherlands on its (cost-)effectiveness and conduct a process evaluation. The computer-assisted reintegration protocol aims to reduce sick leave duration and sick-leave associated costs, with the intention to mitigate the impact of sick leave for both employee and employer. Furthermore, this study might provide valuable insights for the improvement of reintegration guidance for workers with musculoskeletal disorders in general.

详细描述

The objective of the Back on Track study is to evaluate a computer-assisted reintegration protocol for musculoskeletal disorders of a major occupational health service in the Netherlands on its (cost-)effectiveness and conduct a process evaluation. This protocol is characterized by an evidence-based, early, intensive and multidisciplinary approach. A non-randomized controlled study will compare employees on sick leave due to musculoskeletal complaints who are at high risk of long-term sick leave and receive care based on the computer-assisted reintegration protocol (n = 70) with employees receiving usual care (n = 70). The primary outcome will be time until full return to work. Secondary outcomes will include time until partial return to work , full and partial return to work (yes/no), way of return to work (at the own job/company, with our without adjustments), work ability, work productivity, pain, self-reported health and health-related quality of life. Participants will be asked to complete questionnaires at baseline and after three, six, nine and 12 months. Furthermore, data will be obtained from the occupational health service's register. Alongside the effectiveness study, economic and process evaluations will be conducted.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-65 years
  • Self-reported musculoskeletal complaints as primary reason for sick leave
  • High risk of long-term sick leave

排除标准

  • Musculoskeletal complaints due to pregnancy
  • Retirement within one year
  • Sick leave duration of >18 days

研究组 & 干预措施

Intervention: the computer-assisted reintegration protocol for musculoskeletal disorders

Employees on sick leave due to musculoskeletal complaints receiving return-to-work guidance according to the computer-assisted reintegration protocol

干预措施: The computer-assisted reintegration protocol for musculoskeletal disorders (Other)

Control: usual care

Employees on sick leave due to musculoskeletal complaints receiving return-to-work guidance according to usual care.

结局指标

主要结局

Time until full RTW

时间窗: Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).

The number of days from start sick leave until full RTW for at least 28 days.

次要结局

  • Time until partial return to work(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Full return to work(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Partial return to work(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Way of returning to work(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Current work ability(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Presenteeism(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Pain(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Self-reported health(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)
  • Health-related quality of life(Baseline (T0), after 3 months (T1), after 6 months (T2), after 9 months (T3), after 12 months (T4).)

研究者

发起方
Amsterdam UMC, location VUmc
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jantine Maarleveld

PhD Student

Amsterdam UMC, location VUmc

研究点 (1)

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