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临床试验/NCT05546736
NCT05546736尚未招募不适用

Effects of the iCanWork Intervention to Improve Cancer Survivors' Experience With Return to Work: A Randomized Controlled Trial (RCT)

McGill University2 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2023年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
270
试验地点
2
主要终点
Change from baseline return to work status in the course of the 24-month study

研究概览

简要总结

The aim of this study is to evaluate the effectiveness of the iCanWork intervention in assisting cancer survivors (CS) to return to work (RTW) and its impact on their health-related quality of life (QoL), health service utilization, RTW readiness, time to RTW, and work capacity.

详细描述

The iCanWork intervention comprises several elements related to health and work, taken from the latest reviews that recommend a remote and individual intervention, led by a vocational rehabilitation counsellor (VRC), experts in assisting RTW for CS. The intervention includes 6 sessions with a VRC and 1-4 sessions with an occupational therapist (OT). A total of 270 CS will be recruited into 2 groups (intervention or control). The duration of this study is 24 months. Study participants will complete electronic questionnaires measuring study variables at baseline before randomization and at 6-month, 12-month, 18-month, and 24-month follow-ups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

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

  • diagnosed with cancer (all types) treated with curative intent and of working age (between 18 and 65 at the time of diagnosis)
  • gainfully employed at the time of diagnosis (full or part-time, including students)
  • still on sick leave, including long-term disability leave, but for less than 2 years
  • has not started to return to work, since stopping due to cancer
  • can read and understand English or French
  • reside in Canada.

排除标准

  • If the cancer survivor's physicians consider returning to work unwise, such as due to a metastatic cancer diagnosis

结局指标

主要结局

Change from baseline return to work status in the course of the 24-month study

时间窗: baseline, 6 months, 12 months, 18 months, 24 months

binary variable (Yes/No)

次要结局

  • Change from baseline work capacity in the course of the 24-month study(baseline, 6 months, 12 months, 18 months, 24 months)
  • Change from baseline health related quality of life in the course of the 24-month study(baseline, 6 months, 12 months, 18 months, 24 months)
  • Change from baseline readiness to return to work in the course of the 24-month study(baseline, 6 months, 12 months, 18 months, 24 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Christine Maheu

Associate Professor

McGill University

研究点 (2)

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