跳至主要内容
临床试验/NCT06924671
NCT06924671招募中不适用

GLA:D Back Canada - a Program for Persistent Low Back Pain.

University of Alberta1 个研究点 分布在 1 个国家目标入组 2,200 人开始时间: 2021年6月18日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
2,200
试验地点
1
主要终点
Implementation

研究概览

简要总结

GLA:D Back is a program developed in Denmark to help people with persistent low back pain. This study will assist in contextualizing Danish content into an English version of the program.

详细描述

GLA:D Back is a program developed in Denmark to help people with persistent low back pain. Unfortunately, all materials developed for the program are in Danish. In this pilot, the investigators will translate the Danish materials into English, then use them to conduct an English training session for community clinicians in Edmonton, Alberta, Canada. Interested clinicians will then implement the program in their communities and provide feedback to contextualize the program for use in English. Specifically, surveys, interviews and focus groups will be used to help fine-tune the printed content of the course (e.g. manuals), it's training materials (e.g. lectures) and processes related to REDCap data collection (e.g. surveys).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • •Patients must have persistent low back pain of at least 1 month's duration.

排除标准

  • •Participating currently in a supervised exercise or rehabilitation program or enrolled in another interventional clinical trial.
  • •Patients with nerve root involvement, suspected serious pathology, unstable trauma to the spine, aspects of pregnancy or other conditions that would prevent participation or disallow trial completion within the prescribed time period.
  • •Persons with conditions that require a specialist consult are suspected of needing a specialist consult, or have conditions that would be aggravated or worsened if treated by the interventions in this study.

结局指标

主要结局

Implementation

时间窗: 6 months

Number of clinicians who implement the program

次要结局

  • Patients enrolled(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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